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Our specialized team utilizes various networks and have built up an extensive database of high-quality candidates.

Our consultants are resolute professionals who have extensive experience in the Pharmaceutical and Medical fields within large international corporations, and are therefore able to properly identify exactly which candidates best suits our Clients’ requirements.

We pride ourselves on being well-informed and up-to-date on the latest trends in the Pharmaceutical and Medical industry.

Pharmaceutical and Medical Jobs in Africa

The pharmaceutical industry in Africa is growing at a phenomenal rate. With growth rates higher than they’ve ever been in the industry, the race is on for top talent. Formally under the Insurance, Legal and Finance division CA Global now has dedicated staff who specialize in the recruitment of all Pharmaceutical and Medical staff.

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Country Sales Representative ( Chemicals / Raw Materials / Pharma / Distribution / Business Development ) – Nigeria, West Africa.

Job Reference

<p><strong>Reference Number:</strong>158 15 10&nbsp;MNW</p>

<p><strong>Job Description: </strong></p>

<p>Our client is seeking a Technical Sales Representative to handle all sales activities including identifying new business opportunities, grow existing business through product development and expanding customer base in Nigeria. The incumbent will further provide customers with technical advice on raw materials, processing and application formulations.&nbsp;</p>

<p><strong>Responsibilities: </strong></p>

<ul>
<li>Plan and execute sales visits to customers on a regular basis</li>
<li>Maintain a comprehensive contact customer database the all key contact details.</li>
<li>Develop customer intimacy and ensure a thorough understanding of customer needs.</li>
<li>Continuously update customers with current product portfolio and new product development plans.</li>
<li>Point of contact for customers in all aspects, queries re products, orders, deliveries etc;</li>
<li>Monitoring customer accounts to ensure they have sufficient credit limit for future sales and that long outstanding debt relating to queries are resolved timeously;</li>
<li>Assist customers with certificate of analysis, technical data and material safety data sheets; and resolve queries from customers in a timely manner</li>
<li>Ensure prompt dispatch of sample materials and follow up with customer</li>
<li>Monitor market trends and competitor activities and the reporting thereof to the Sub-Sahara Pharma Director</li>
<li>Maintain up-to-date market information and information on potential business opportunities/market.</li>
<li>Understand the industry in terms of customer business, market/industry trends, product application knowledge and competitive strengths.</li>
<li>Planning of supplier visits to ensure all key customer visits are made in a timely manner</li>
<li>Update supplier on all the market activities and discuss both opportunities and risks in the market</li>
<li>Comprehensive visit reports should be sent to supplier on all visits and shared with the Sub Saharan Pharma Director</li>
<li>Planning and coordination of supplier visit schedule which should be confirmed early to avoid visitor conflicts and overwhelming customers with repeat visits.</li>
<li>Support the Sub Saharan Pharma Director with general operations to help the team reaching sales objectives.</li>
<li>Communicate and coordinate closely all orders with the internal sales representative</li>
<li>Ongoing communication with Finance and Warehouse and logistics teams</li>
</ul>

<p><strong>Requirements</strong><strong>:</strong> <strong>Qualification and Skill<em> </em></strong></p>

<ul>
<li>Tertiary education in Chemical / Pharma etc.</li>
<li>Minimum 5 years sales experience</li>
</ul>

<p><strong>Benefits and Contractual information:</strong></p>

<ul>
<li>Permanent local contract</li>
</ul>

<p>&nbsp;</p>

<p>If you wish to apply for the position please <strong>send your CV </strong>to <strong>Mitchill Wernich </strong>at <strong><a href="mailto:mwernich@camining.com">mwernich@camining.com</a> </strong></p>

<p>Please visit <strong><a href="http://www.camining.com">www.camining.com</a> </strong>for more exciting opportunities.</p>

<p>&nbsp;</p>

<p><strong>Mitchill Wernich</strong></p>

<p>Recruitment Consultant&nbsp;</p>

<p><strong>CA Mining</strong></p>

<p>CA Mining will respond to short-listed candidates only. If you have not had any response in two weeks, please consider your application unsuccessful however your CV will be kept on our database for any other suitable positions.</p>

<p>&nbsp;</p>

Region

Western Africa#Central Africa

Technical Advisor (Vaccines / Health and Manufacturing / COVID-19) – Remote, South Africa

Job Reference

<p><strong>Reference Number: LBGLK005</strong></p>

<p> </p>

<p><strong>Job Description:</strong></p>

<p>An exciting global pharmaceutical client of ours is looking to hire a Technical Advisor who is an expert in vaccines and will be responsible for the implementation of technical assistance activities for COVID-19 vaccine manufacturing and regulation. They will report to the in-country Chief of Party or their designee and will work under technical guidance and oversight from the HQ-based Vaccines Director. The Technical Advisor will provide support to local manufacturers of vaccines in Africa in technology transfer and will help build national regulatory capacity for vaccines as well as the workforce competency for biologics and vaccines quality assurance. The successful candidate will provide technical assistance on fill/finish and packaging processes for COVID-19 vaccines. They will serve as a subject matter expert using knowledge to ensure cGMP compliance, fulfillment of technical requirements and regulatory guidelines as they relate to fill/finish and packaging equipment, materials, facilities, and process development. In fulfillment of the role, the incumbent will collaborate with other staff of the organization, their Global Biologics Division, local manufacturers, and vaccine regulators.</p>

<p> </p>

<p><strong>Responsibilities:</strong></p>

<ul>
<li>Lead and coordinate the technical development and implementation of in-country COVID-19 vaccine manufacturing and regulatory work plan activities.</li>
<li>Provide technical assistance to COVID-19 mRNA vaccines manufacturers on development, commissioning, qualification and validation of vaccine fill/finish and packaging processes.</li>
<li>Partner with the organization’s technical team members, consultants, other countries, vendors, and local stakeholders to assure adequate manufacturing facility design and startup.</li>
<li>Provide support to strengthen the National Medicines Regulatory Authority (NMRA) legal framework for vaccines manufacturing, supply, storage, distribution, and handling.</li>
<li>Support NMRA and national control labs in the development of lot release testing capacity and in the implementation of vaccine post-marketing surveillance.</li>
<li>Support the GMP inspectorate of the NMRA to strengthen its capacity for regulatory oversight of vaccine manufacturers.</li>
<li>Liaise with HQ Vaccines Director to develop appropriate training materials and to organize the delivery of training programs targeted to local vaccine manufacturers, regulators, and quality laboratory staff.</li>
<li>Support manufacturers in addressing deviations and non-compliances, in conducting audits to assess compliance and the establishment of cGMPs.</li>
<li>Filing of vaccine dossiers for market authorization according to NMRA’s requirements.</li>
<li>Coordinate efforts aimed at the identification of needs for manufacturing and laboratory equipment, materials, and processes in support to successful local production and quality assurance of COVID-19 vaccines.</li>
<li>Support manufacturers to identify chemistry, manufacturing, and controls (CMC) risks and continuous improvement opportunities.</li>
<li>Gather programmatic data and develop progress reports as guided by the organizations HQ Vaccines Director.</li>
<li>Support the development of technical and communication materials related to local manufacturing and quality of vaccines.</li>
</ul>

<p><strong>Requirements:</strong></p>

<ul>
<li>Master of Science or PhD in pharmacy, pharmaceutical science, chemistry, biochemistry, engineering, or science related field of study.</li>
<li>Bachelor of Science degree in pharmacy, pharmaceutical science, chemistry, biochemistry, engineering, or science related field of study required.</li>
<li>Understanding of GMP manufacturing of biologics, including vaccines</li>
<li>Understanding of compatibility and stability studies.</li>
<li>Understanding of cold chain monitoring.</li>
<li>Understanding of fill/finish and packaging processes for mRNA vaccines.</li>
<li>Direct experience with and understanding of WHO vaccine pre-qualification and/or other regulatory authority registration processes.</li>
<li>10+ years of experience in vaccines and biologics manufacturing or regulation.</li>
<li>Subject matter expert in vaccine/biopharmaceutical fill/finish and packaging processes.</li>
<li>Thorough understanding of Chemistry, Manufacturing and Controls and Good Manufacturing Practices for vaccines and medicines e.g., fill and finish.</li>
<li>Knowledge of regulatory requirements related to the development and manufacture of biologics</li>
<li>Strong technical writing and oral communication skills.</li>
</ul>

<p><strong>Contractual information:</strong></p>

<ul>
<li>Willingness to travel up to 25% of the time.</li><li><span lang="EN-US" style="text-align: justify; text-indent: -18pt; font-size: 10pt;">Positions will be 1-year fixed term contact with
the potential of being extended.</span><p class="MsoListParagraph" style="margin-top:0cm;margin-right:0cm;margin-bottom:
0cm;margin-left:22.5pt;text-align:justify;text-indent:-18.0pt;line-height:normal;
mso-list:l0 level1 lfo1"><span lang="EN-US" style="font-size:10.0pt;
mso-bidi-font-family:Calibri"><o:p></o:p></span></p></li>
</ul>

<p>Please visit <strong>www.caglobalint.com</strong> for more exciting opportunities.</p>

<p> </p>

<p><strong>Leroy Gona</strong></p>

<p>Recruitment Consultant</p>

<p><strong>CA Global Finance</strong></p>

<p> </p>

<p>CA Global will respond to short-listed candidates only. If you have not had any response in two weeks, please consider your application unsuccessful however your CV will be kept on our database for any other suitable positions.</p>

Region

Southern Africa

Technical Advisor (Vaccines / Health and Manufacturing / COVID-19) – Lagos, Nigeria

Job Reference

<div>
<div>
<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Reference Number: CDTTA1</span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Job Description: </span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">An exciting global pharmaceutical client of ours is looking to hire a Technical Advisor who is an expert in vaccines and will be responsible for the implementation of technical assistance activities for COVID-19 vaccine manufacturing and regulation. They will report to the in-country Chief of Party or their designee and will work under technical guidance and oversight from the HQ-based Vaccines Director. The Technical Advisor will provide support to local manufacturers of vaccines in Africa in technology transfer and will help build national regulatory capacity for vaccines as well as the workforce competency for biologics and vaccines quality assurance. The successful candidate will provide technical assistance on fill/finish and packaging processes for COVID-19 vaccines. They will serve as a subject matter expert using knowledge to ensure cGMP compliance, fulfillment of technical requirements and regulatory guidelines as they relate to fill/finish and packaging equipment, materials, facilities, and process development. In fulfillment of the role, the incumbent will collaborate with other staff of the organization, their Global Biologics Division, local manufacturers, and vaccine regulators. </span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Responsibilities<em>: </em></span></span></strong></span></span></p>

<ul>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Lead and coordinate the technical development and implementation of in-country COVID-19 vaccine manufacturing and regulatory work plan activities</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Provide technical assistance to COVID-19 mRNA vaccines manufacturers on development, commissioning, qualification and validation of vaccine fill/finish and packaging processes</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Partner with the organization&rsquo;s technical team members, consultants, other countries, vendors, and local stakeholders to assure adequate manufacturing facility design and startup</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Provide support to strengthen the National Medicines Regulatory Authority (NMRA) legal framework for vaccines manufacturing, supply, storage, distribution, and handling </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Support NMRA and national control labs in the development of lot release testing capacity and in the implementation of vaccine post-marketing surveillance </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Support the GMP inspectorate of the NMRA to strengthen its capacity for regulatory oversight of vaccine manufacturers&nbsp; </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Liaise with HQ Vaccines Director to develop appropriate training materials and to organize the delivery of training programs targeted to local vaccine manufacturers, regulators, and quality laboratory staff</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Support manufacturers in addressing deviations and non-compliances, in conducting audits to assess compliance and the establishment of cGMPs</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Filing of vaccine dossiers for market authorization according to NMRA&rsquo;s requirements</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Coordinate efforts aimed at the identification of needs for manufacturing and laboratory equipment, materials, and processes in support to successful local production and quality assurance of COVID-19 vaccines </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Support manufacturers to identify chemistry, manufacturing, and controls (CMC) risks and continuous improvement opportunities </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Gather programmatic data and develop progress reports as guided by the organizations HQ Vaccines Director</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Support the development of technical and communication materials related to local manufacturing and quality of vaccines </span></span></span></span></li>
</ul>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Requirements</span></span></strong><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">:</span></span></strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif"> </span></span></span></span></p>

<ul>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Master of Science or PhD in pharmacy, pharmaceutical science, chemistry, biochemistry, engineering, or science related field of study</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Bachelor of Science degree in pharmacy, pharmaceutical science, chemistry, biochemistry, engineering, or science related field of study required </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Understanding of GMP manufacturing of biologics, including vaccines</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Understanding of compatibility and stability studies</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Understanding of cold chain monitoring</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Understanding of fill/finish and packaging processes for mRNA vaccines</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Direct experience with and understanding of WHO vaccine pre-qualification and/or other regulatory authority registration processes</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">8+ years of experience in vaccines and biologics manufacturing or regulation </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Subject matter expert in vaccine/biopharmaceutical fill/finish and packaging processes</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Thorough understanding of Chemistry, Manufacturing and Controls and Good Manufacturing Practices for vaccines and medicines e.g., fill and finish</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Knowledge of regulatory requirements related to the development and manufacture of biologics</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Strong technical writing and oral communication skills</span></span></span></span></li>
</ul>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Contractual information:</span></span></strong></span></span></p>

<ul>
<li style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt">Willingness to travel up to 25% of the time</span></span></span></li>
</ul>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">If you wish to apply for the position, please <strong>send your CV </strong>to <strong>Chalden Du Toit </strong>at <strong>cdutoit@caglobalint.com</strong></span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Please visit <strong><a href="http://www.caglobalint.com" style="color:blue; text-decoration:underline">www.caglobalint.com</a> </strong>for more exciting opportunities. </span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Chalden du Toit</span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Recruitment Consultant</span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">CA Global Finance</span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">CA Global will respond to short-listed candidates only. If you have not had any response in two weeks, please consider your application unsuccessful however your CV will be kept on our database for any other suitable positions.</span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>
</div>
</div>

Region

Southern Africa

Chief Of Party (Pharmaceuticals / Health / Strategy / USAID) – Kigali, Rwanda

Job Reference

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Reference Number: CDTCOPR</span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Job Description:</span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm; text-align:justify"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif"><span style="color:black">A leading international pharmaceutical client of our is currently looking to hire The Chief of Party, who is the Country lead management position for the country program. The Chief of Party provides overall in-country leadership for strategy, management, and program implementation to achieve the program&rsquo;s goal towards sustainably strengthening medical product quality assurance systems. (S)he ensures consistent, effective, and compliant country program operations and the timely delivery of products that meet work plan objectives that are aligned with the priority needs of the country quality assurance systems and stakeholders&rsquo; expectations. The Chief of Party serves as the primary liaison with USAID, relevant government agencies, and key stakeholders to ensure achievement of program deliverables, and to ensure that the program activities complement on-going initiatives. The Chief of Party will manage a team of staff in achieving program results while maintaining operational excellence. </span></span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Responsibilities<em>: </em></span></span></strong></span></span></p>

<ul>
<li><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt">Provides strategic leadership and oversight for overall management of the country program. This includes but is not limited to leading program design and developing work plans, leading overall implementation of project activities, and setting performance targets to meet priority needs of the country quality assurance systems and stakeholders&rsquo; expectations.</span></span></span></li>
<li><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt">Leads the implementation of program activities, monitor program progress, account for deliverables, monitor that the implementation of activities are of high quality, and produce timely quarterly and annual progress reports</span></span></span></li>
<li><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt">Accountable for the overall program operations, financial and contractual management, and compliance with USAID regulations. </span></span></span></li>
<li><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt">Oversees the accuracy, clarity, and quality of progress reports and other project documentation necessary for USAID reporting, ensuring they are completed in accordance with USAID and company policies and procedures and submitted in a timely manner.</span></span></span></li>
<li><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt">Oversees all human resources and personnel management issues and tasks, including recruitment, onboarding of local staff and performance management to ensure compliance of established policies and procedures</span></span></span></li>
<li><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt">Represent the Program and increase the program&rsquo;s visibility among key stakeholders through networking and active participation at relevant meetings and forums; engage with other Implementing Partners to take advantage of opportunities for leveraging existing initiatives and sharing of best practices.</span></span></span></li>
<li><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt">Develops and maintain strong working relationships with senior government officials, head of Agencies, leaders of pharmaceutical associations, donors, and other in-country stakeholders.</span></span></span></li>
</ul>

<p>&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Requirements</span></span></strong><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">:</span></span></strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif"> </span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif"><span style="color:black">Basic Qualifications:</span></span></span></span></span></p>

<ul>
<li><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt">Master&#39;s degree in a health-related field required</span></span></span></li>
<li><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt">Minimum of 10+ years of professional experience in the successful implementation of donor-funded programs with a minimum of 8 years&rsquo; relevant experience leading and managing diverse teams on USAID- funded global health program implementation and project management.</span></span></span></li>
<li><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt">Demonstrated knowledge of USAID rules, regulations and reporting requirements </span></span></span></li>
<li><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt">Deep understanding of pharmaceutical management issues in public health programs and challenges for meeting global health objectives.</span></span></span></li>
</ul>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Preferred Qualifications:</span></span></span></span></p>

<ul>
<li><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt">Pharmacist, medical doctor or other health profession qualification highly desirable</span></span></span></li>
<li><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt">Expertise in health systems strengthening preferred.</span></span></span></li>
<li><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt">Significant experience working with high level officials in USAID and country governments; existing relationships with key donors and implementing partners working on health and pharmaceutical systems strengthening preferred</span></span></span></li>
<li><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt">Strong people management skills, including of virtual, matrixed teams</span></span></span></li>
<li><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt">Excellent client relationship management skills </span></span></span></li>
<li><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt">Excellent written and verbal communication skills</span></span></span></li>
<li><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt">Ability to work in cross-cultural settings. </span></span></span></li>
<li><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt">Ability to demonstrate highest degree of ethics and integrity.&nbsp; </span></span></span></li>
<li><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt">Ability to travel up to 25% time. </span></span></span></li>
</ul>

<p style="margin-left:36pt; margin-right:0cm; text-align:justify">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">If you wish to apply for the position, please <strong>send your CV </strong>to <strong>Chalden Du Toit </strong>at <strong>cdutoit@caglobalint.com</strong></span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Please visit <strong><a href="http://www.caglobalint.com">www.caglobalint.com</a> </strong>for more exciting opportunities. </span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Chalden du Toit</span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Recruitment Consultant</span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">CA Global Finance</span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">CA Global will respond to short-listed candidates only. If you have not had any response in two weeks, please consider your application unsuccessful however your CV will be kept on our database for any other suitable positions.</span></span></span></span></p>

<div>
<div>
<p>&nbsp;</p>

<p>&nbsp;</p>
</div>
</div>

Region

Eastern Africa#Central Africa

Regional Technical Sales Representative ( Chemicals / Raw Materials / Pharma / Distribution / Business Development ) – Ghana, West Africa.

Job Reference

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Reference Number:</span></span></strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif"> 125 25 06 MNW</span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Job Description: </span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Our client is seeking a Technical Sales Representative to handle all sales activities including identifying new business opportunities, grow existing business through product development and expanding customer base in Ghana. The incumbent will further provide customers with technical advice on raw materials, processing and application formulations.&nbsp; </span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Responsibilities: </span></span></strong></span></span></p>

<ul>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Plan and execute sales visits to customers on a regular basis</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Maintain a comprehensive contact customer database the all key contact details.</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Develop customer intimacy and ensure a thorough understanding of customer needs.</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Continuously update customers with current product portfolio and new product development plans.</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Point of contact for customers in all aspects, queries re products, orders, deliveries etc;</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Monitoring customer accounts to ensure they have sufficient credit limit for future sales and that long outstanding debt relating to queries are resolved timeously;</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Assist customers with certificate of analysis, technical data and material safety data sheets; and resolve queries from customers in a timely manner</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Ensure prompt dispatch of sample materials and follow up with customer</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Monitor market trends and competitor activities and the reporting thereof to the Sub-Sahara Pharma Director</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Maintain up-to-date market information and information on potential business opportunities/market.</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Understand the industry in terms of customer business, market/industry trends, product application knowledge and competitive strengths.</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Planning of supplier visits to ensure all key customer visits are made in a timely manner</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Update supplier on all the market activities and discuss both opportunities and risks in the market</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Comprehensive visit reports should be sent to supplier on all visits and shared with the Sub Saharan Pharma Director</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Planning and coordination of supplier visit schedule which should be confirmed early to avoid visitor conflicts and overwhelming customers with repeat visits. </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Support the Sub Saharan Pharma Director with general operations to help the team reaching sales objectives.</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Communicate and coordinate closely all orders with the internal sales representative</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Ongoing communication with Finance and Warehouse and logistics teams</span></span></span></span></li>
</ul>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Requirements</span></span></strong><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">:</span></span></strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif"> <strong>Qualification and Skill<em> </em></strong></span></span></span></span></p>

<ul>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Tertiary education in Chemical / Pharma etc. </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Minimum 5 years sales experience </span></span></span></span></li>
</ul>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Benefits and Contractual information:</span></span></strong></span></span></p>

<ul>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Permanent local contract </span></span></span></span></li>
</ul>

<p>&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">If you wish to apply for the position please <strong>send your CV </strong>to <strong>Mitchill Wernich </strong>at <strong><a href="mailto:mwernich@camining.com" style="color:blue; text-decoration:underline">mwernich@camining.com</a> </strong></span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Please visit <strong><a href="http://www.camining.com" style="color:blue; text-decoration:underline">www.camining.com</a> </strong>for more exciting opportunities. </span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Mitchill Wernich</span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Recruitment Consultant&nbsp;</span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">CA Mining</span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">CA Mining will respond to short-listed candidates only. If you have not had any response in two weeks, please consider your application unsuccessful however your CV will be kept on our database for any other suitable positions.</span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

Region

Western Africa

Senior Program Manager (Vaccines / Health and Manufacturing / Pharmaceuticals / NGO Experience / Project Management) – Remote, South Africa

Job Reference

<p><strong>Reference Number: LBGLK008</strong></p>

<p>&nbsp;</p>

<p><strong>Job Description:</strong></p>

<p>An exciting global pharmaceutical client of ours is looking to hire a Senior Program Manager. The Senior Program Manager will be based in South Africa, work as part of a team to design and manage the implementation of donor-funded project activities in client&rsquo;s Global Health and Manufacturing Services (GHMS) Division, specifically activities related to Covid-19 vaccine roll-out in South Africa and the region under a USAID-funded project. The Senior Program Manager will provide the day-to-day program management oversight of assigned projects, including development of workplans, implementation and monitoring of project activities, drafting of progress reports, and development and management of project budgets, to ensure high quality results and the overall success and integrity of the project. The Senior Program Manager is responsible for providing strategic management in client assigned countries to achieve program and country goals and ensure that activities are based and informed by country needs and priorities. The Senior Program Manager may supervise a team that may include program managers and program associates, as well as short-term and long-term consultants. The incumbent will report to the Deputy Director.</p>

<p>&nbsp;</p>

<p><strong>Responsibilities:</strong></p>

<ul>
<li>Participates in strategic planning discussions and leads the design of project activities in close collaboration with the Vaccine Director, client&rsquo;s leadership, and other staff.</li>
<li>Supervises program managers and associates that support countries in the portfolio, as well as consultants as assigned.</li>
<li>Under the supervision and guidance of the Vaccine Director leads the planning and implementation of the assigned project activities to include development of annual workplans, activity monitoring matrices/implementation plans, performance monitoring plans, and progress reports with the support of the M&amp;E team.</li>
<li>Collaborates with the in-county teams and HQ staff to ensure the documentation of the program activities, highlighting technical and programmatic innovations, strengths, results.</li>
<li>Leads cross-functional project management teams to include technical, M&amp;E, and finance staff to produce high-quality work under tight deadlines, while remaining within the defined project scope and budget.</li>
<li>Manages timelines/deadlines and provides quality control support for project deliverables to ensure effective, efficient, and compliant project implementation.</li>
<li>Works closely with technical team and country program teams to identify opportunities for innovation, harmonize approaches, and maintain high quality standards in activity implementation.</li>
<li>Develops scopes of work and manage sub-awardees, consultants, and vendors, as applicable while ensuring compliance to donor rules and regulations and client&rsquo;s policies.</li>
<li>Delivers timely and high-quality donor reports; ensures M&amp;E data is regularly collected and documented; and works with other staff, including field staff, to develop global reports that demonstrate progress towards achieving specific targets.</li>
<li>Proactively anticipates, identifies, and facilitates resolution of potential project issues and risks relating to delays in implementation of project activities.</li>
<li>Develops project budgets and monitors project expenditures to ensure activities are implemented within budget and prepares pipelines/projections as needed in collaboration with Finance staff.</li>
<li>Develops effective working relationships with USAID, and other donors and key partners; and represents client at key stakeholder meetings.</li>
<li>Collaborates with external partners including other international and local partners in-country to jointly achieve the public health program goals. Designs programs and create business opportunities for program growth and sustainability.</li>
<li>Manages performance and career development goals for direct report and ensure client&rsquo;s processes and timelines for documentation are adhered to.</li>
<li>Ensures good records management, according to client and donor&rsquo;s policies.</li>
</ul>

<p>&nbsp;</p>

<p><strong>Requirements:</strong></p>

<ul>
<li>Master&rsquo;s degree in pharmaceutical sciences, public health, or related field required</li>
<li>Minimum of 8 Years of experience managing donor-funded (e.g., USAID) global health projects</li>
<li>Demonstrated ability to work independently and manage multiple workflows, while effectively managing project timelines and deliverable schedules.</li>
<li>Strong written and oral communication skills</li>
<li>Strong communication skills and fluent in English language.</li>
<li>Knowledge of USAID policies and procedures and prior management of USAID-Funded programs.</li>
<li>Ability to build relationships and interact effectively with technical experts, other partners, and donor agencies.</li>
</ul>

<p>&nbsp;</p>

<p><strong>Contractual information:</strong></p>

<ul>
<li>Authorized to work in South Africa.</li>
<li>Position is currently remote but will become an in-office role at a later stage.</li>
<li>Willingness to travel up to 20% of the time.</li>
</ul>

<p>&nbsp;</p>

<p>Please visit www.caglobalint.com for more exciting opportunities.</p>

<p>&nbsp;</p>

<p><strong>Leroy Gona</strong></p>

<p>Recruitment Consultant</p>

<p><strong>CA Finance</strong></p>

<p>&nbsp;</p>

<p>CA Global will respond to short-listed candidates only. If you have not had any response in two weeks, please consider your application unsuccessful however your CV will be kept on our database for any other suitable positions.</p>

Region

Southern Africa

Manager: Procurement Excellence (Procurement / Supplier Relationship / Governance) – Gauteng, South Africa

Job Reference

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Job Description: </span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Our client is a large banking firm seeking to employ Manager: Procurement for their offices located in Gauteng, South Africa.&nbsp; The main purpose of this position is to lead the Procurement Excellence Section, which includes Governance, Supplier Relationship Management, Contracts Administration, Reporting and Data Analytics, to ensure that the Procurement Division delivers its mandate within a predefined framework and policy.</span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Responsibilities: </span></span></strong></span></span></p>

<ul>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Develop, review and maintain the Procurement Policy, Procedural Guidelines and any applicable Terms of Reference (ToR), templates, checklists and flowcharts.</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Advise on, and facilitate the effective implementation of, the principles contained in the Procurement Policy, Procedural Guidelines and any applicable ToR throughout the Group.</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Manage the outputs of the section, which include Governance, Risk and Compliance (GRC), Supplier Relationship Management (SRM), Contracts Administration, Meta-data Management, Reporting and Data Analytics.&nbsp; </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Provide strategic guidance to the SRM lead and collaborate with the sourcing teams on strategic supplier management and supplier risk management.</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Collaborate and liaise with the Legal Services Department (LSD) for mitigation of potential procurement risks as due to new legislation and relevant case law.&nbsp; </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Analyse and integrate management information relating to the divisional outputs for reporting purposes (Sourcing, Supplier Relationship Management, Procurement Governance Risk and Compliance). </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Create awareness of Procurement GRC, SRM and develop training material; facilitate training workshops for staff members from the Procurement Division or to any other business departments.</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Facilitate and conduct quality assurance reviews to check for compliance with the Procurement Policy, Procedural Guidelines and any applicable ToR and investigate instances of non-compliance and facilitate the implementation of corrective measures.</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Monitor, manage and mitigate procurement risks in accordance with the Procurement Governance and Risk Management Framework. </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Stay abreast of any new developments and best practice in the procurement domain and apply in functional area. </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Facilitate and coordinate internal and external audit activities relating to the Procurement Division.</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Liaise with LSD and business to facilitate the effective management of procurement contracts throughout the contract management lifecycle.</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Manage and enhance relationships of the Procurement Division with relevant internal and external stakeholders.&nbsp; </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Manage the performance and development of staff in the section, provide technical coaching and guidance, and motivate the team to deliver results.</span></span></span></span></li>
</ul>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Requirements</span></span></strong><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">:</span></span></strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif"> <strong>Qualification and Skill<em> </em></strong></span></span></span></span></p>

<ul>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">a minimum of a bachelor&rsquo;s degree in Commerce, Law, Supply Chain Management (NQF 7) or an equivalent qualification; and</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">8‒10 years of working experience in a supply chain, legal governance, or business governance.</span></span></span></span></li>
</ul>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Additional requirements are as follows:</span></span></strong></span></span></p>

<ul>
<li style="margin-left: 0cm; margin-right: 0cm;"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">a post graduate qualification/certification (added advantage) </span></span></span></span></li>
<li style="margin-left: 0cm; margin-right: 0cm;"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">industry, organisational and business awareness knowledge and skills.</span></span></span></span></li>
<li style="margin-left: 0cm; margin-right: 0cm;"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">quality assurance knowledge and skills.</span></span></span></span></li>
<li style="margin-left: 0cm; margin-right: 0cm;"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">continuous improvement knowledge and skills.</span></span></span></span></li>
<li style="margin-left: 0cm; margin-right: 0cm;"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">continued learning and/or professional development knowledge and skills.</span></span></span></span></li>
<li style="margin-left: 0cm; margin-right: 0cm;"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">tactical sourcing.</span></span></span></span></li>
<li style="margin-left: 0cm; margin-right: 0cm;"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">risk profiling.</span></span></span></span></li>
<li style="margin-left: 0cm; margin-right: 0cm;"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">financial analysis.</span></span></span></span></li>
<li style="margin-left: 0cm; margin-right: 0cm;"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">enterprise resource planning (ERP).</span></span></span></span></li>
<li style="margin-left: 0cm; margin-right: 0cm;"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">supply chain management.</span></span></span></span></li>
<li style="margin-left: 0cm; margin-right: 0cm;"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">project management.</span></span></span></span></li>
<li style="margin-left: 0cm; margin-right: 0cm;"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">business process optimization.</span></span></span></span></li>
<li style="margin-left: 0cm; margin-right: 0cm;"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">relevant legislation.</span></span></span></span></li>
<li style="margin-left: 0cm; margin-right: 0cm;"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">computer literacy.</span></span></span></span></li>
<li style="margin-left: 0cm; margin-right: 0cm;"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">conceptual thinking.</span></span></span></span></li>
<li style="margin-left: 0cm; margin-right: 0cm;"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">drive for results.</span></span></span></span></li>
<li style="margin-left: 0cm; margin-right: 0cm;"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">building and managing relationships.</span></span></span></span></li>
<li style="margin-left: 0cm; margin-right: 0cm;"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">problem solving and analysis.</span></span></span></span></li>
<li style="margin-left: 0cm; margin-right: 0cm;"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">effective communication (verbal and written English language)</span></span></span></span></li>
<li style="margin-left: 0cm; margin-right: 0cm;"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">planning and organizing.</span></span></span></span></li>
<li style="margin-left: 0cm; margin-right: 0cm;"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">judgement and decision-making.</span></span></span></span></li>
<li style="margin-left: 0cm; margin-right: 0cm;"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">service and stakeholder focus; and </span></span></span></span></li>
<li style="margin-left: 0cm; margin-right: 0cm;"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">impact and influence.</span></span></span></span></li>
</ul>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">If you wish to apply for the position, please <strong>send your CV </strong>to <strong>srabsch@caglobalint.com </strong></span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Please visit <strong><a href="http://www.caglobalint.com" style="color:blue; text-decoration:underline">www.caglobalint.com</a></strong> for more exciting opportunities. </span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Shearidan Rabsch</span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Managing Consultant</span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">CA Finance &ndash; Banking, Insurance, Legal and Finance</span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">CA Global will respond to short-listed candidates only. If you have not had any response in two weeks, please consider your application unsuccessful however your CV will be kept on our database for any other suitable positions.</span></span></span></span></p>

Region

Southern Africa

Technical Advisor (Vaccines / Health and Manufacturing / COVID-19) – Kigali, Rwanda

Job Reference

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Reference Number: CDTTA2</span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Job Description: </span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">An exciting global pharmaceutical client of ours is looking to hire a Technical Advisor who is an expert in vaccines and will be responsible for the implementation of technical assistance activities for COVID-19 vaccine manufacturing and regulation. They will report to the in-country Chief of Party or their designee and will work under technical guidance and oversight from the HQ-based Vaccines Director. The Technical Advisor will provide support to local manufacturers of vaccines in Africa in technology transfer and will help build national regulatory capacity for vaccines as well as the workforce competency for biologics and vaccines quality assurance. The successful candidate will provide technical assistance on fill/finish and packaging processes for COVID-19 vaccines. They will serve as a subject matter expert using knowledge to ensure cGMP compliance, fulfillment of technical requirements and regulatory guidelines as they relate to fill/finish and packaging equipment, materials, facilities, and process development. In fulfillment of the role, the incumbent will collaborate with other staff of the organization, their Global Biologics Division, local manufacturers, and vaccine regulators. </span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Responsibilities<em>: </em></span></span></strong></span></span></p>

<ul>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Lead and coordinate the technical development and implementation of in-country COVID-19 vaccine manufacturing and regulatory work plan activities</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Provide technical assistance to COVID-19 mRNA vaccines manufacturers on development, commissioning, qualification and validation of vaccine fill/finish and packaging processes</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Partner with the organization&rsquo;s technical team members, consultants, other countries, vendors, and local stakeholders to assure adequate manufacturing facility design and startup</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Provide support to strengthen the National Medicines Regulatory Authority (NMRA) legal framework for vaccines manufacturing, supply, storage, distribution, and handling </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Support NMRA and national control labs in the development of lot release testing capacity and in the implementation of vaccine post-marketing surveillance </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Support the GMP inspectorate of the NMRA to strengthen its capacity for regulatory oversight of vaccine manufacturers&nbsp; </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Liaise with HQ Vaccines Director to develop appropriate training materials and to organize the delivery of training programs targeted to local vaccine manufacturers, regulators, and quality laboratory staff</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Support manufacturers in addressing deviations and non-compliances, in conducting audits to assess compliance and the establishment of cGMPs</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Filing of vaccine dossiers for market authorization according to NMRA&rsquo;s requirements</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Coordinate efforts aimed at the identification of needs for manufacturing and laboratory equipment, materials, and processes in support to successful local production and quality assurance of COVID-19 vaccines </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Support manufacturers to identify chemistry, manufacturing, and controls (CMC) risks and continuous improvement opportunities </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Gather programmatic data and develop progress reports as guided by the organizations HQ Vaccines Director</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Support the development of technical and communication materials related to local manufacturing and quality of vaccines </span></span></span></span></li>
</ul>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Requirements</span></span></strong><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">:</span></span></strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif"> </span></span></span></span></p>

<ul>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Master of Science or PhD in pharmacy, pharmaceutical science, chemistry, biochemistry, engineering, or science related field of study</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Bachelor of Science degree in pharmacy, pharmaceutical science, chemistry, biochemistry, engineering, or science related field of study required </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Understanding of GMP manufacturing of biologics, including vaccines</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Understanding of compatibility and stability studies</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Understanding of cold chain monitoring</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Understanding of fill/finish and packaging processes for mRNA vaccines</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Direct experience with and understanding of WHO vaccine pre-qualification and/or other regulatory authority registration processes</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">8+ years of experience in vaccines and biologics manufacturing or regulation </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Subject matter expert in vaccine/biopharmaceutical fill/finish and packaging processes</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Thorough understanding of Chemistry, Manufacturing and Controls and Good Manufacturing Practices for vaccines and medicines e.g., fill and finish</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Knowledge of regulatory requirements related to the development and manufacture of biologics</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Strong technical writing and oral communication skills</span></span></span></span></li>
</ul>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Contractual information:</span></span></strong></span></span></p>

<ul>
<li style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt">Willingness to travel up to 25% of the time</span></span></span></li>
</ul>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">If you wish to apply for the position, please <strong>send your CV </strong>to <strong>Chalden Du Toit </strong>at <strong>cdutoit@caglobalint.com</strong></span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Please visit <strong><a href="http://www.caglobalint.com" style="color:blue; text-decoration:underline">www.caglobalint.com</a> </strong>for more exciting opportunities. </span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Chalden du Toit</span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Recruitment Consultant</span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">CA Global Finance</span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">CA Global will respond to short-listed candidates only. If you have not had any response in two weeks, please consider your application unsuccessful however your CV will be kept on our database for any other suitable positions.</span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

Region

Southern Africa

Technical Advisor (Vaccines / Health and Manufacturing / COVID-19) – Remote, Senegal

Job Reference

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Job Description: </span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">An exciting global pharmaceutical client of ours is looking to hire a Technical Advisor who is an expert in vaccines and will be responsible for the implementation of technical assistance activities for COVID-19 vaccine manufacturing and regulation. They will report to the in-country Chief of Party or their designee and will work under technical guidance and oversight from the HQ-based Vaccines Director. The Technical Advisor will provide support to local manufacturers of vaccines in Africa in technology transfer and will help build national regulatory capacity for vaccines as well as the workforce competency for biologics and vaccines quality assurance. The successful candidate will provide technical assistance on fill/finish and packaging processes for COVID-19 vaccines. They will serve as a subject matter expert using knowledge to ensure cGMP compliance, fulfillment of technical requirements and regulatory guidelines as they relate to fill/finish and packaging equipment, materials, facilities, and process development. In fulfillment of the role, the incumbent will collaborate with other staff of the organization, their Global Biologics Division, local manufacturers, and vaccine regulators. </span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Responsibilities<em>: </em></span></span></strong></span></span></p>

<ul>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Lead and coordinate the technical development and implementation of in-country COVID-19 vaccine manufacturing and regulatory work plan activities</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Provide technical assistance to COVID-19 mRNA vaccines manufacturers on development, commissioning, qualification and validation of vaccine fill/finish and packaging processes</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Partner with the organization&rsquo;s technical team members, consultants, other countries, vendors, and local stakeholders to assure adequate manufacturing facility design and startup</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Provide support to strengthen the National Medicines Regulatory Authority (NMRA) legal framework for vaccines manufacturing, supply, storage, distribution, and handling </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Support NMRA and national control labs in the development of lot release testing capacity and in the implementation of vaccine post-marketing surveillance </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Support the GMP inspectorate of the NMRA to strengthen its capacity for regulatory oversight of vaccine manufacturers&nbsp; </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Liaise with HQ Vaccines Director to develop appropriate training materials and to organize the delivery of training programs targeted to local vaccine manufacturers, regulators, and quality laboratory staff</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Support manufacturers in addressing deviations and non-compliances, in conducting audits to assess compliance and the establishment of cGMPs</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Filing of vaccine dossiers for market authorization according to NMRA&rsquo;s requirements</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Coordinate efforts aimed at the identification of needs for manufacturing and laboratory equipment, materials, and processes in support to successful local production and quality assurance of COVID-19 vaccines </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Support manufacturers to identify chemistry, manufacturing, and controls (CMC) risks and continuous improvement opportunities </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Gather programmatic data and develop progress reports as guided by the organizations HQ Vaccines Director</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Support the development of technical and communication materials related to local manufacturing and quality of vaccines </span></span></span></span></li>
</ul>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Requirements</span></span></strong><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">:</span></span></strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif"> </span></span></span></span></p>

<ul>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Master of Science or PhD in pharmacy, pharmaceutical science, chemistry, biochemistry, engineering, or science related field of study</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Bachelor of Science degree in pharmacy, pharmaceutical science, chemistry, biochemistry, engineering, or science related field of study required </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Understanding of GMP manufacturing of biologics, including vaccines</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Understanding of compatibility and stability studies</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Understanding of cold chain monitoring</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Understanding of fill/finish and packaging processes for mRNA vaccines</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Direct experience with and understanding of WHO vaccine pre-qualification and/or other regulatory authority registration processes</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">8+ years of experience in vaccines and biologics manufacturing or regulation </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Subject matter expert in vaccine/biopharmaceutical fill/finish and packaging processes</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Thorough understanding of Chemistry, Manufacturing and Controls and Good Manufacturing Practices for vaccines and medicines e.g., fill and finish</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Knowledge of regulatory requirements related to the development and manufacture of biologics</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Strong technical writing and oral communication skills</span></span></span></span></li>
</ul>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Contractual information:</span></span></strong></span></span></p>

<ul>
<li style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt">Willingness to travel up to 25% of the time</span></span></span></li>
</ul>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">If you wish to apply for the position, please <strong>send your CV </strong>to <strong>Jamie Adams </strong>at <strong>jadams@caglobalint.com</strong></span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Please visit <strong><a href="http://www.caglobalint.com" style="color:blue; text-decoration:underline">www.caglobalint.com</a> </strong>for more exciting opportunities. </span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Jamie Adams</span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Recruitment Specialist&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">CA Finance</span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">CA Global will respond to short-listed candidates only. If you have not had any response in two weeks, please consider your application unsuccessful however your CV will be kept on our database for any other suitable positions.</span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

Region

Western Africa

Technical Advisor (Vaccines / Health and Manufacturing / COVID-19) – Kwabenya, Ghana

Job Reference

<p><strong>Reference Number: LBGLK006</strong></p>

<p>&nbsp;</p>

<p><strong>Job Description:</strong></p>

<p>An exciting global pharmaceutical client of ours is looking to hire a Technical Advisor who is an expert in vaccines and will be responsible for the implementation of technical assistance activities for COVID-19 vaccine manufacturing and regulation. They will report to the in-country Chief of Party or their designee and will work under technical guidance and oversight from the HQ-based Vaccines Director. The Technical Advisor will provide support to local manufacturers of vaccines in Africa in technology transfer and will help build national regulatory capacity for vaccines as well as the workforce competency for biologics and vaccines quality assurance. The successful candidate will provide technical assistance on fill/finish and packaging processes for COVID-19 vaccines. They will serve as a subject matter expert using knowledge to ensure cGMP compliance, fulfillment of technical requirements and regulatory guidelines as they relate to fill/finish and packaging equipment, materials, facilities, and process development. In fulfillment of the role, the incumbent will collaborate with other staff of the organization, their Global Biologics Division, local manufacturers, and vaccine regulators.</p>

<p>&nbsp;</p>

<p><strong>Responsibilities:</strong></p>

<ul>
<li>Lead and coordinate the technical development and implementation of in-country COVID-19 vaccine manufacturing and regulatory work plan activities.</li>
<li>Provide technical assistance to COVID-19 mRNA vaccines manufacturers on development, commissioning, qualification and validation of vaccine fill/finish and packaging processes.</li>
<li>Partner with the organization’s technical team members, consultants, other countries, vendors, and local stakeholders to assure adequate manufacturing facility design and startup.</li>
<li>Provide support to strengthen the National Medicines Regulatory Authority (NMRA) legal framework for vaccines manufacturing, supply, storage, distribution, and handling.</li>
<li>Support NMRA and national control labs in the development of lot release testing capacity and in the implementation of vaccine post-marketing surveillance.</li>
<li>Support the GMP inspectorate of the NMRA to strengthen its capacity for regulatory oversight of vaccine manufacturers.</li>
<li>Liaise with HQ Vaccines Director to develop appropriate training materials and to organize the delivery of training programs targeted to local vaccine manufacturers, regulators, and quality laboratory staff.</li>
<li>Support manufacturers in addressing deviations and non-compliances, in conducting audits to assess compliance and the establishment of cGMPs.</li>
<li>Filing of vaccine dossiers for market authorization according to NMRA’s requirements.</li>
<li>Coordinate efforts aimed at the identification of needs for manufacturing and laboratory equipment, materials, and processes in support to successful local production and quality assurance of COVID-19 vaccines.</li>
<li>Support manufacturers to identify chemistry, manufacturing, and controls (CMC) risks and continuous improvement opportunities.</li>
<li>Gather programmatic data and develop progress reports as guided by the organizations HQ Vaccines Director.</li>
<li>Support the development of technical and communication materials related to local manufacturing and quality of vaccines.</li>
</ul>

<p><strong>Requirements:</strong></p>

<ul>
<li>Master of Science or PhD in pharmacy, pharmaceutical science, chemistry, biochemistry, engineering, or science related field of study.</li>
<li>Bachelor of Science degree in pharmacy, pharmaceutical science, chemistry, biochemistry, engineering, or science related field of study required.</li>
<li>Understanding of GMP manufacturing of biologics, including vaccines</li>
<li>Understanding of compatibility and stability studies.</li>
<li>Understanding of cold chain monitoring.</li>
<li>Understanding of fill/finish and packaging processes for mRNA vaccines.</li>
<li>Direct experience with and understanding of WHO vaccine pre-qualification and/or other regulatory authority registration processes.</li>
<li>10+ years of experience in vaccines and biologics manufacturing or regulation.</li>
<li>Subject matter expert in vaccine/biopharmaceutical fill/finish and packaging processes.</li>
<li>Thorough understanding of Chemistry, Manufacturing and Controls and Good Manufacturing Practices for vaccines and medicines e.g., fill and finish.</li>
<li>Knowledge of regulatory requirements related to the development and manufacture of biologics</li>
<li>Strong technical writing and oral communication skills.</li>
</ul>

<p><strong>Contractual information:</strong></p>

<ul>
<li>Willingness to travel up to 25% of the time.</li><li>Positions will be 1-year fixed term contact with
the potential of being extended.</li>
</ul>

<p>Please visit&nbsp;<strong>www.caglobalint.com</strong>&nbsp;for more exciting opportunities.</p>

<p>&nbsp;</p>

<p><strong>Leroy Gona</strong></p>

<p>Recruitment Consultant</p>

<p><strong>CA Global Finance</strong></p>

<p>&nbsp;</p>

<p>CA Global will respond to short-listed candidates only. If you have not had any response in two weeks, please consider your application unsuccessful however your CV will be kept on our database for any other suitable positions.</p>

Region

Western Africa

Finance and Operations Manager (Accounting / Administration / Pharmaceuticals) Madagascar

Job Reference

<div>
<div>
<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif"><span style="color:black">Reference Number: CDTFOM1</span></span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif"><span style="color:black">Job Description: </span></span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm; text-align:justify"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif"><span style="color:black">Working under the direction and guidance of the Madagascar based Program Lead with dotted line reporting to the home office Director for Finance and Operations, the Finance &amp; Operations Manager will be responsible for overseeing the overall country office operations, including leading the start-up of country operations, for the Promoting of the program. This role is responsible and accountable for effective and efficient operations of the country office to include management of all financial, accounting, and administrative functions, such as procurement and inventory tracking, human resources, and safety and security in accordance with the company, and in country regulations for the program.&nbsp; The Finance &amp; Operations Manager will maintain frequent communication with the company&rsquo;s HQ, including the Finance &amp; Operations Director, Global Finance, HR, and the Finance and Operations Manager, and serve as a member of the leadership team. This position will oversee the Madagascar branches budget development, expenditure monitoring, and managing of all accounts payable functions to include processing payroll, processing invoices, and analyzing accounts and tax returns according to local statutory requirements. S/he will be also responsible for coordinating with required audit functions, including providing necessary financial information, compiling, and submitting reports. S/He will also ensure compliance with USAID and Government of Madagascar regulations by leading the implementation of the company&rsquo;s financial management policies and procedures.</span></span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm; text-align:justify">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif"><span style="color:black">Responsibilities: </span></span></span></strong></span></span></p>

<ul>
<li style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Adopts and implements the company&rsquo;s policies and procedures in compliance with the company, USAID and Government regulations and manages finances and accounting, budgeting and audits as set by HQ. </span></span></span></span></li>
<li style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Provides training to local staff to ensure overall compliance with operational policies and procedures.&nbsp; </span></span></span></span></li>
<li style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Leads and develops annual project budgets/forecasts and monitors spend on a monthly basis to ensure activities are implemented within budget and conducts financial review and analysis to alert management of issues/risks related to budget spend.</span></span></span></span></li>
<li style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Monitors the field offices cash balances and submits monthly cash requests to the company&rsquo;s home office for approval. </span></span></span></span></li>
<li style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Manages day-to-day accounting operations to include review of all accounting transactions to ensure adequate supporting documentation, accuracy of amounts and project coding, and necessary internal controls over payments</span></span></span></span></li>
<li style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Maintains system of accounts ensuring all accounting data are updated, reconciled and fully supported</span></span></span></span></li>
<li style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Manages preparation and submission of required monthly reconciliation and financial reports to HQ and coordinates with the Finance &amp; Operations Director and Director Eastern and Southern Africa on financial reports requested.</span></span></span></span></li>
<li style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Serves as Liaison with external auditors, facilitates internal and external audit undertakings, prepares responses to audit findings and follows-up on the implementation of audit recommendations in collaboration with Global Finance</span></span></span></span></li>
<li style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Processes and manages VAT Exemptions via USAID mechanism</span></span></span></span></li>
<li style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Liaise with headquarters, USAID, partners, banks, and Government official (Ministry of Finance &ndash; Tax Office)</span></span></span></span></li>
<li style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Maintains accounting controls by ensuring the implementation of financial management policies and procedures.</span></span></span></span></li>
<li style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Performs other tasks as assigned. </span></span></span></span></li>
</ul>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif"><span style="color:black">Human Resources Management </span></span></span></strong></span></span></p>

<ul>
<li style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Manages local Human Resources processes in accordance with local labor laws in collaboration with HQ, including contracts, compensation packages and working hours</span></span></span></span></li>
<li style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Manages in-country recruitment process to ensure compliance with the company&rsquo;s policies and procedures and leads new hire onboarding in collaboration with HQ </span></span></span></span></li>
<li style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Overseas performance management process and support in ensuring high engagement of staff</span></span></span></span></li>
<li style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Acts as point of contact in country for any performance management issues that may arise and partner with HQ-HR on resolution of issues</span></span></span></span></li>
<li style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Ensures staff complete timesheets per the company&rsquo;s policies, and systems are in place to track accrued vacation/personal leave </span></span></span></span></li>
<li style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Maintains employee records and files in country</span></span></span></span></li>
</ul>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif"><span style="color:black">Administration </span></span></span></strong></span></span></p>

<ul>
<li><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Oversees logistics including management of travel arrangements, meeting/workshop logistical arrangements, etc. to support effective and efficient project implementation</span></span></span></span></li>
<li><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Manages office inventory /assets and government property, as applicable in compliance with USAID rules and regulations </span></span></span></span></li>
<li><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Manages IT vendors and coordinates with regional IT staff to address any issues related to IT operations (hardware, software, and access to systems)</span></span></span></span></li>
<li><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Serves as in-country Security Focal Point and coordinates with Global Security to maintain safety and security of staff and visitors</span></span></span></span></li>
<li><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Ensures that the in- country legal registrations are current and adequate, and that the country office is in compliance with local labor and other relevant regulations.</span></span></span></span></li>
<li><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Ensures that the country office management is efficient, effective and conducive to promoting an enjoyable place to work where staff can thrive and engage one another.</span></span></span></span></li>
<li><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Develops and maintains a comprehensive and efficient filing system for good records keeping and document management.</span></span></span></span></li>
<li><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Trains and mentors finance and operations staff in an effort to continuously build capacity of the in-country staff</span></span></span></span></li>
</ul>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif"><span style="color:black">Requirements: Qualifications &amp; Skills</span></span></span></strong></span></span></p>

<ul>
<li style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Bachelor&rsquo;s degree in finance, accounting or a professional equivalent</span></span></span></span></li>
<li style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Minimum of 8 years of progressive professional accounting experience and /or financial management or master&rsquo;s degree in finance, accounting, or related field</span></span></span></span></li>
<li style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Minimum of 5 years of demonstrated experience (Including people management) in finance and administration/operations of a USG funded project</span></span></span></span></li>
<li><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Knowledge of applicable Malagasy, rules and regulations, and policies governing financial and administrative processes. </span></span></span></span></li>
<li><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">General knowledge and understanding of donor funded business development.</span></span></span></span></li>
<li><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Experience filing statutory Malagasy taxes and managing office financial environment.</span></span></span></span></li>
<li><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Demonstrated experience with MS Excel, word PowerPoint, and accounting software, experience with QuickBooks preferred.</span></span></span></span></li>
<li><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Meticulous attention to detail, as well as outstanding critical thinking and problem-solving skills. </span></span></span></span></li>
<li><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Demonstrated ability to work both independently and as a member of a team, show initiative, solve problems, handle multiple tasks simultaneously and remain calm under pressure</span></span></span></span></li>
<li><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Ability to work independently and as part of a team.</span></span></span></span></li>
<li><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Ability to influence without direct authority.</span></span></span></span></li>
<li><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Ability and desire to work well with diverse employees and customers in a cooperative and friendly manner.</span></span></span></span></li>
<li><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Ability to handle multiple priorities in a fast-paced environment and meeting deadlines; results-oriented.</span></span></span></span></li>
<li><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Excellent written and verbal communications skills.</span></span></span></span></li>
<li style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="color:black">Proven capability to productively support internal and external staff and be a team player.</span></span></span></span></li>
</ul>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif"><span style="color:black">If you wish to apply for the position, please <strong>send your CV </strong>to <strong>Chalden Du Toit </strong>at <strong>Cdutoit@caglobalint.com</strong></span></span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif"><span style="color:black">Please visit <strong><a href="http://www.caglobalint.com"><span style="color:black">www.caglobalint.com</span></a> </strong>for more exciting opportunities. </span></span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif"><span style="color:black">Chalden Du Toit</span></span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif"><span style="color:black">Recruitment Specialist&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span></span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif"><span style="color:black">CA Global Finance</span></span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif"><span style="color:black">CA Global will respond to short-listed candidates only. If you have not had any response in two weeks, please consider your application unsuccessful however your CV will be kept on our database for any other suitable positions.</span></span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p>&nbsp;</p>
</div>
</div>

<p>&nbsp;</p>

Region

Southern Africa

Senior Technical Officer - Regulatory Systems Strengthening

Job Reference

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Job Description: </span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">An exciting global pharmaceutical client of ours is looking to hire a Senior Technical Officer - Regulatory Systems Strengthening(STO-RSS) must have expert skills in key pharmaceutical regulatory functions including Post-Marketing Surveillance (PMS), Quality Management Systems (QMS), Product Evaluation and Registration, Good Manufacturing Practices (GMP) and Good Distribution Practices (GDP) and others. The STO-RSS will provide technical assistance to the National Medicines Regularity Authority &ldquo;Agence du Medicament de Madagascar&rdquo; (AMM) and to the Ministry of Health to build their capacity to regulate pharmaceutical products in Madagascar. The selected candidate will work with other PQM+ team members to assist AMM to implement relevant actions listed in the institutional development plan (IDP) of the agency, focusing on the PMS and other core regulatory functions, which will help improve WHO-GBT Maturity Level of AMM. He/she will provide technical oversight of the PMS and QMS related components of the PQM+&rsquo;s objective of improving country and regional regulatory systems to assure the quality of medical products in the public and private sectors.</span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Responsibilities<em>: </em></span></span></strong></span></span></p>

<ul>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Provide technical oversight of activities to support the regulatory functions of AMM</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Work with AMM to implement relevant actions listed in the institutional development plan (IDP) of the authority, focusing on PMS and other core regulatory functions, to assist the AMM improve the WHO-Global Benchmarking Tool (WHO-GBT) Maturity Level rating.</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Implement PQM+ technical activities under the guidance of the regional and US Rockville-based technical teams.</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Propose, design, and implement interventions aimed at strengthening the PMS, QMS and other core regulatory functions including the development and implementation of protocols, guidelines, procedures, and other relevant tools.</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Provide technical leadership and support to improve efficiency, effectiveness, and sustainability of PMS and other core regulatory processes.</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Work closely with AMM to support development and deployment of strategies towards improvement of national regulatory systems. </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Actively contribute to annual programmatic and resource planning process and development of quarterly and annual reports.</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Support development of country work plans and budgets.</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Collect and report program data and indicators; documents and translates program information; and helps in coordinating in-country program logistics for implementation of workplan activities.</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Lead and manages other PQM+ local staff and consultants in Madagascar.</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Performs other duties as assigned by the senior program manager.</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Travel in Africa 25% of the time.</span></span></span></span></li>
</ul>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Requirements</span></span></strong><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">:</span></span></strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif"> </span></span></span></span></p>

<ul>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Bachelor&rsquo;s degree in pharmaceutical sciences</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">At least 8 years&rsquo; hands-on experience working in pharmaceutical regulation, quality management systems or pharmaceutical quality control </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Master&rsquo;s degree in pharmaceutical sciences/pharmaceutical quality assurance and quality control of medicines is beneficial.</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Post-qualification training and implementation in pharmaceutical quality management systems is beneficial.</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Strong technical writing and communication skills and fluent in spoken and written English language. </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Ability to build relationships and interact effectively with technical experts, other partners, and donor agencies. </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Experience working with USAID projects preferred.</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Must possess ability to work independently and handle multiple priorities in a fast-paced environment</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Skills in training and workshop facilitation desired </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Demonstratable highest degree of ethics and integrity.</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Excellent interpersonal, leadership and organizational skills with strong attention to detail. </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Results driven with demonstrated successful outcomes</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Experience in managing and leading technical teams</span></span></span></span></li>
</ul>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">If you wish to apply for the position, please <strong>send your CV </strong>to <strong>Jamie Adams </strong>at <strong>jadams@caglobalint.com</strong></span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Please visit <strong><a href="http://www.caglobalint.com" style="color:blue; text-decoration:underline">www.caglobalint.com</a> </strong>for more exciting opportunities. </span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Jamie Adams</span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Recruitment Specialist&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">CA Finance</span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">CA Global will respond to short-listed candidates only. If you have not had any response in two weeks, please consider your application unsuccessful however your CV will be kept on our database for any other suitable positions.</span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

Region

Southern Africa

Director: Health Standards Development And Training (Healthcare / Regulations / Compliance) Pretoria, South Africa

Job Reference

<div>
<div>
<p><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Reference Number: CDTDHS</span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Job Description: </span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:11.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">A client of ours within the health sector is currently seeking a Director of Health Standards Development and Training, who will be responsible for developing the health standards framework and measure compliance with health standards. </span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Responsibilities: </span></span></strong></span></span></p>

<ul>
<li><span style="font-size:12pt"><span style="font-family:Calibri,sans-serif"><span style="color:black"><span style="font-size:11.0pt">Develop and implement the Health Standards research, design and development management framework.</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:Calibri,sans-serif"><span style="color:black"><span style="font-size:11.0pt">Direct the drafting, testing, validation, and periodic review of tools to measure compliance with health &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;standards and norms.</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:Calibri,sans-serif"><span style="color:black"><span style="font-size:11.0pt">Direct the drafting, consuitation and finalization of health standards for consideration by the Minister and publication for public comments.</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:Calibri,sans-serif"><span style="color:black"><span style="font-size:11.0pt">Direct the capability development of OHSC compliance inspectors, complaints assessors and investigators.</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:Calibri,sans-serif"><span style="color:black"><span style="font-size:11.0pt">Direct the management of health standards guidance and support. General management of staff and other resources in accordance with OHSC policies and any other reasonable responsibilities.</span></span></span></span></li>
</ul>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Requirements</span></span></strong><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">:</span></span></strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif"> </span></span></span></span></p>

<ul>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:11.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif"><span style="color:black">An MBChB or a bachelor&rsquo;s degree in Nursing.</span></span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:11.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif"><span style="color:black">A post graduate qualification in Public Health or Quality Management would be an advantage.</span></span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:11.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif"><span style="color:black">A minimum of eight (8) years&rsquo; experience in direct patient care and /or health care management of which five (5) years must have been at a middle management or equivalent level.</span></span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:11.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif"><span style="color:black">Experience must also include the development or review of health standards for regulations and measurement tools.</span></span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:11.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif"><span style="color:black">Knowledge of the norms and standards for health establishments.</span></span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:11.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif"><span style="color:black">Excellent communication, analytical and report writing skills.</span></span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:11.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif"><span style="color:black">A valid driver&rsquo;s license.</span></span></span></span></span></li>
</ul>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">If you wish to apply for the position, please <strong>send your CV </strong>to <strong>Chalden Du Toit </strong>at <strong><a href="mailto:cdutoit@caglobalint.com" style="color:blue; text-decoration:underline">cdutoit@caglobalint.com</a></strong></span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Please visit <strong><a href="http://www.caglobalint.com" style="color:blue; text-decoration:underline">www.caglobalint.com</a> </strong>for more exciting opportunities. </span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Chalden Du Toit</span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Recruitment Consultant</span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">CA Finance</span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">CA Global will respond to short-listed candidates only. If you have not had any response in two weeks, please consider your application unsuccessful however your CV will be kept on our database for any other suitable positions.</span></span></span></span></p>
</div>
</div>

Region

Southern Africa

Technical Advisor (Vaccines / Health and Manufacturing / COVID-19) – Nairobi, Kenya

Job Reference

<div>
<div>
<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Reference Number: CDTTA3</span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Job Description: </span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">An exciting global pharmaceutical client of ours is looking to hire a Technical Advisor who is an expert in vaccines and will be responsible for the implementation of technical assistance activities for COVID-19 vaccine manufacturing and regulation. They will report to the in-country Chief of Party or their designee and will work under technical guidance and oversight from the HQ-based Vaccines Director. The Technical Advisor will provide support to local manufacturers of vaccines in Africa in technology transfer and will help build national regulatory capacity for vaccines as well as the workforce competency for biologics and vaccines quality assurance. The successful candidate will provide technical assistance on fill/finish and packaging processes for COVID-19 vaccines. They will serve as a subject matter expert using knowledge to ensure cGMP compliance, fulfillment of technical requirements and regulatory guidelines as they relate to fill/finish and packaging equipment, materials, facilities, and process development. In fulfillment of the role, the incumbent will collaborate with other staff of the organization, their Global Biologics Division, local manufacturers, and vaccine regulators. </span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Responsibilities<em>: </em></span></span></strong></span></span></p>

<ul>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Lead and coordinate the technical development and implementation of in-country COVID-19 vaccine manufacturing and regulatory work plan activities</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Provide technical assistance to COVID-19 mRNA vaccines manufacturers on development, commissioning, qualification and validation of vaccine fill/finish and packaging processes</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Partner with the organization&rsquo;s technical team members, consultants, other countries, vendors, and local stakeholders to assure adequate manufacturing facility design and startup</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Provide support to strengthen the National Medicines Regulatory Authority (NMRA) legal framework for vaccines manufacturing, supply, storage, distribution, and handling </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Support NMRA and national control labs in the development of lot release testing capacity and in the implementation of vaccine post-marketing surveillance </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Support the GMP inspectorate of the NMRA to strengthen its capacity for regulatory oversight of vaccine manufacturers&nbsp; </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Liaise with HQ Vaccines Director to develop appropriate training materials and to organize the delivery of training programs targeted to local vaccine manufacturers, regulators, and quality laboratory staff</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Support manufacturers in addressing deviations and non-compliances, in conducting audits to assess compliance and the establishment of cGMPs</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Filing of vaccine dossiers for market authorization according to NMRA&rsquo;s requirements</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Coordinate efforts aimed at the identification of needs for manufacturing and laboratory equipment, materials, and processes in support to successful local production and quality assurance of COVID-19 vaccines </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Support manufacturers to identify chemistry, manufacturing, and controls (CMC) risks and continuous improvement opportunities </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Gather programmatic data and develop progress reports as guided by the organizations HQ Vaccines Director</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Support the development of technical and communication materials related to local manufacturing and quality of vaccines </span></span></span></span></li>
</ul>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Requirements</span></span></strong><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">:</span></span></strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif"> </span></span></span></span></p>

<ul>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Master of Science or PhD in pharmacy, pharmaceutical science, chemistry, biochemistry, engineering, or science related field of study</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Bachelor of Science degree in pharmacy, pharmaceutical science, chemistry, biochemistry, engineering, or science related field of study required </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Understanding of GMP manufacturing of biologics, including vaccines</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Understanding of compatibility and stability studies</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Understanding of cold chain monitoring</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Understanding of fill/finish and packaging processes for mRNA vaccines</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Direct experience with and understanding of WHO vaccine pre-qualification and/or other regulatory authority registration processes</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">10+ years of experience in vaccines and biologics manufacturing or regulation </span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Subject matter expert in vaccine/biopharmaceutical fill/finish and packaging processes</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Thorough understanding of Chemistry, Manufacturing and Controls and Good Manufacturing Practices for vaccines and medicines e.g., fill and finish</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Knowledge of regulatory requirements related to the development and manufacture of biologics</span></span></span></span></li>
<li><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Strong technical writing and oral communication skills</span></span></span></span></li>
</ul>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Contractual information:</span></span></strong></span></span></p>

<ul>
<li style="text-align:justify"><span style="font-size:11pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt">Willingness to travel up to 25% of the time</span></span></span></li>
</ul>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">If you wish to apply for the position, please <strong>send your CV </strong>to <strong>Chalden Du Toit </strong>at <strong>cdutoit@caglobalint.com</strong></span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Please visit <strong><a href="http://www.caglobalint.com" style="color:blue; text-decoration:underline">www.caglobalint.com</a> </strong>for more exciting opportunities. </span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Chalden du Toit</span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">Recruitment Consultant</span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">CA Global Finance</span></span></strong></span></span></p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>

<p style="margin-left:0cm; margin-right:0cm"><span style="font-size:12pt"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Calibri&quot;,sans-serif">CA Global will respond to short-listed candidates only. If you have not had any response in two weeks, please consider your application unsuccessful however your CV will be kept on our database for any other suitable positions.</span></span></span></span></p>

<p style="margin-left:0cm; margin-right:0cm">&nbsp;</p>
</div>
</div>

Region

Southern Africa

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