Summary
Date Posted: Thursday, December 01, 2022 , Base Salary: Not Disclosed

JOB DETAILS:
Purpose of consultancy
To provide technical expertise to the Local Production & Assistance (LPA) Unit with programme activities in strengthening local production and technology transfer for improving access to quality-assured, safe and effective in-vitro diagnostics and other medical devices.

Deliverables:
The consultant will provide:
• Specialized Prequalification (PQ)-related technical assistance, for up to 10 manufacturers such as assessments/verification of the quality/CMC aspects and the dossier of vaccines and other biological/pharmaceutical products with the relevant documents (e.g. reports).
• PQ-related specialized technical assistance for up to 10 manufacturers with on-site/virtual training and/or technical assistance on the quality/CMC aspects and/or dossier of vaccines and other biological/pharmaceutical products, and the relevant documents (e.g., concept note, agenda, reports).
• Technical input for a standard operation procedure for provision of PQ-related specialized technical assistance to manufacturers of vaccines and other biological products and deliver relevant documentation (e.g. SoP document).
• On-site reviews of dossiers of vaccines and/or biological/pharmaceutical products for compliance with current WHO/international quality standards and requirements, including for WHO PQ/EUL, conducted in up to 4 countries and preparation of relevant documents (e.g. reports).
• At least 2 capacity building activities and technical assistance activities, organized and conducted for relevant stakeholders in the areas of CMC/quality, dossiers, etc. of vaccines and/or biological/pharmaceutical products with the relevant documents (e.g. concept note, agenda).
• Training materials prepared related on the quality/CMC aspects of vaccines and/or other biological/pharmaceutical products.
• Technical input on the technical products of the LPA Unit, such as ”frequently asked questions” documents, with collaboration from relevant colleagues.

Qualifications, experience, skills and languages
Educational Qualifications:
Essential:
• Advanced university degree in pharmacy, sciences, life sciences or other health or socio-economic related fields.

Desirable:
• Advanced university degree related to development and/or production of vaccines and/or biological products, such as immunology, biochemistry, cellular biology or biotechnology.

Experience
Essential:
• At least seven years of relevant experience, some of which at the international level, in the production, CMC, quality control and dossier preparation for vaccines and/or biological products under current international quality standards.

Desirable:
• Experience in the production, CMC and/or quality control of vaccines/biological products;
• Experience in a national regulatory authority as a CMC/quality assessor of vaccines/biological products;
• Experience with the WHO Prequalification and/or Emergency Use Listing procedures;
• Experience in organizing and/or providing capacity building/training for quality production of medical products in low- and middle-income countries;
• Experience in technology transfers; and/or in an international organization.

Relevant professional experience in the medical product manufacturing industry including:
Skills/Knowledge:
Essential:
• Strong knowledge of the manufacturing processes, CMC and product dossier requirements of vaccines and biological products in accordance with WHO and/or internationally-recognized standards;
• Knowledge of current WHO and other internationally-recognized quality assurance standards, WHO emergency listing and/or prequalification procedures and/or health product regulation for vaccines and biological products;
• Ability to review, revise or develop technical documents and activities in the area of local production of medical products;
• Ability to design, plan and implement activities to achieve the goal(s);
• Excellent communication and interpersonal skills, strong planning and organizational skills and ability to use a range of IT tools (Word, Excel, presentation software, databases and web navigators;
• Demonstrated ability to interact with all stakeholders with tact and diplomacy, upholding the reputation of the Organization at all times.

Desirable:
• Knowledge of current WHO and/or other internationally recognized standards of GMP and/or quality management systems of manufacturing facilities of vaccines and biological products;
• Knowledge of technology transfers for vaccines and/or biological/pharmaceutical products;
• Knowledge of the CMC, GMP and/or product dossier requirements of medicines in accordance with WHO and/or internationally-recognized standards.


Work Hours: 8

Experience in Months: 84

Level of Education: Postgraduate Degree

Job application procedure

Use the link(s) below to apply on company website.
Consultant –Local production and assistance in Product Chemistry, Manufacturing and Controls (CMC)/Quality and Dossier

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