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Validation Engineer

Escalate Life Sciences
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Validation Specialist support commissioning, qualification and validation (CQV) activities for the cGMP manufacturing facility at MA site. Scope of work is expected to include routine qualification, requalification and decommissioning (Facilities, Utilities System and Equipment) support for all CQV activities for the following:

Clean Rooms and Utilities
Manufacturing Activities
Analytical QC instruments and equipment
Supply Chain equipment
Controlled Temperature Units (Stand-ups and Walk-Ins), Warehouse