Global Vaccine and Biotherapeutic Product Expert

Vor 5 Tagen

Genf, Genf, Schweiz WHO Vollzeit

Overview

The World Health Organization (WHO) is seeking an experienced expert in vaccine and biotherapeutic product development, production, and regulation to support our efforts in strengthening local production of vaccines and biotherapeutic products.

Job Description

We are looking for a highly skilled professional with a strong background in manufacturing processes, quality control, and regulatory affairs. The successful candidate will work closely with our team to provide technical assistance and capacity building activities to manufacturers of vaccines and biotherapeutic products in low- and middle-income countries.

Main Responsibilities:

  • Provide technical assistance and training to manufacturers on WHO and internationally recognized quality standards, GMP, and product dossier requirements;
  • Contribute to the development of standard operation procedures for provision of WHO PQ-related specialized technical assistance;
  • Facilitate on-site reviews of dossiers of vaccines and/or biotherapeutic products for compliance with current WHO/international standards and requirements;
  • Organize and conduct capacity building activities and technical assistance activities for relevant stakeholders in the areas of CMC/quality, non-clinical, clinical, and post-marketing safety documentation, etc.;
  • Design, plan, and implement activities to achieve the goal(s);
  • Interact with all stakeholders with tact and diplomacy, upholding the reputation of the Organization at all times;

Requirements:

  • Advanced university degree in pharmacy, health sciences, life sciences, or other science or health-related fields;
  • At least seven years of relevant experience, some of which at the international level, in the production, CMC, quality control, non-clinical, and/or clinical development, post-marketing safety documentation, and dossier preparation for vaccines and/or biotherapeutic products under current international quality standards;
  • Strong knowledge of manufacturing processes, CMC, non-clinical, and/or clinical development, post-marketing safety documentation, and product dossier requirements of vaccines and/or biotherapeutic products in accordance with WHO and/or internationally recognized standards;
  • Ability to review, revise, or develop technical documents and activities in the area of local production of medical products;
  • Excellent communication and interpersonal skills, strong planning and organizational skills, and ability to use a range of IT tools;

Benefits:

  • A competitive salary ranging from USD 7,000 to 9,980 per month, depending on experience;
  • Travel opportunities to support our global efforts in strengthening local production of vaccines and biotherapeutic products;

Contract Terms:

  • 2-11 months duration;
  • Full-time and part-time roles considered;

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