QC Validation Supervisor

Our client, a multinational company in the pharmaceutical industry requires a QC Validation Supervisor

Start: ASAP
Duration: at least until 31/12/13 + possibility of being extended
Location: South of Brussels

FUNCTION DESCRIPTION:
Physico chemistry QC method validation Superviseur:
- Write validation documentation according to 'Re Validation Assessment' (RVA)
- Re Validation Assessment to write
- Follow quality parameters for physico chemistry QC department
- Write validation documentation for new method or to answer toauthorities
- Tests procedure Update and validity criteria update in testing procedure according to validation results
- QC work

KEY RESPONSIBILITIES:
- writing documentation for physicochemistry QC method validation (inEnglish): protocols and reports
- Respect the global planning
- Ensure compliance with policies, processes and guidelines

PREREQUISITES
Education: min BAC + 5 level Chemist or biochemist

Knowledge:
- knowledge of physicochemistry QC method validation
- cGMP knowledge

Experience:
- Experience in a pharmaceutical QC laboratory
- physicochemistry: HPLC, colorimetric assay,
- experience SAP if possible.

Language requirements: Bilingual French/English