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CQV Engineer
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Full-time
- DPS Group has an excellent opportunity for a Validation/CQV Engineer to join our team in supporting our world-class, innovative BioPharma client in the greater Philadelphia, PA area.
- Support project Equipment Validation (i.e. autoclave, bioreactor) – Lab/cGMP.
- Review requirements and source documentation P&IDs, RDs, URSs, SOPs, Specifications), for use in the development of equipment commissioning and validation documents
- Execution of equipment validation protocols (including use of Kaye Validator/temperature monitoring for autoclaves, SIP Systems, washer COP, CIP, FITs, etc.)
- Equipment Validation/CQV experience working within a cGMP & FDA Regulated environment is preferred.
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