· Perform routine environmental sampling (non-viable particle, viable particle and surface) in controlled environmental areas.
· Ensure EM equipment is calibrated before due date and perform EM data entry and analysis
· Participates in Method Verification and Method Validation when required
· Ensure a healthy inventory to support EM sampling
· Practise 6S and ensure good housekeeping
· Ensure compliance to cGMP and EHSS requirements at all times
· Diploma/NITEC in Microbiology/Biotechnology/Biology with 1 - 2 years of relevant QA experience in the pharmaceutical or relevant industry.
· Laboratory experience is essential.
· Knowledge of clean room process with cGLP and cGMP knowledge.
Interested candidate can email directly to: ngee-mien.n.quek@gsk.com
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