E-MED:OMS/Poste pour la pr�-qualification des fournisseurs/produits
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Vacancy Notice No.: HQ/02/HTP/TA16
http://erecruit.who.int/e-jobs/public/hrd-cl-vac-view.cfm?jobinfo_uid_c=176&
vaclng=en
Title: Technical Officer
Deadline for applications : 6 January 2003
17 day(s) until closing deadline
Grade: P-4
Contract type: Temporary appointment
Duration: Five months
Duty Station: GENEVA Switzerland
Organizational Unit:
Health Technology and Pharmaceuticals (HTP)
Essential Drugs and Medicines Policy (EDM )
Quality Assurance and Safety: Medicines (QSM)
INTRODUCTION:
Description of duties
Pre-qualification of pharmaceutical products and suppliers: HIV/AIDS,
Malaria, Tuberculosis
1. Model Quality Assurance System
- To assist the Project Manager in establishing the Model Quality Assurance
System that can be used in various
organizations, more specifically for United Nations procurement
organizations in cooperation with other supply agencies.
2. Operational Procedures and related documentation
- To assist in the drafting, review and maintenance of a documented quality
system for the pre-qualification process of pharmaceutical products.
- Liaise with other staff members in EDM in the development, implementation
and review of guidelines related to EDM/QSM activities, norms and
standards.
3. Pre-qualification of suppliers of HIV/AIDS, antimalarial and anti-TB
drugs
- Assist in the establishment of essential requirements for quality
specifications for these groups of pharmaceutical products, based on
existing WHO norms, standards and related guidelines.
- Manage the assessment of the dossiers submitted in terms of the
pre-qualification process, including formalising reports and communications
to interested and participating manufacturers and suppliers.
- Compose teams for the evaluation and assessment of the dossiers.
- Assist in researching information, report writing and presentation of
information, data and results, including training
material.
4. Related activities
- Prepare written achievement reports and progress reports on the
assessment.
- Work in cooperation with the Project Manager and Secretary.
QUALIFICATIONS REQUIRED:
Education
University degree in pharmacy or medicine.
Skills and Competencies
Sound general knowledge of drug registration, preferably with in-depth
knowledge of registration of generic drugs.
Experience
At least five years' regulatory experience..
Languages
Excellent knowledge of English or French with a good working knowledge of
the other language.
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