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CQV Engineer
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Full-time
- Review requirements and source documentation P&IDs, RDs, URSs, SOPs, Specifications), for use in development of equipment commissioning and validation documents.
- Equipment validation protocol development, including drafting documents, managing review cycles and protocol approval.
- Preparation and processing of turnover packaging and validation documentation in EDMS (electronic document management system).
- BS (MS preferred), in Industrial, Process or Chemical Engineering
- Knowledge of typical biotech/pharmaceutical manufacturing systems and equipment
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