- Verista (New Brunswick, NJ)
- …and learn from our experiences to enhance our collective expertise Lead CQV Engineer /Analyst Responsibilities: + Authoring, editing, and executing technical ... process knowledge + Understanding validation documents, URS, IQ, OQ, PQ + Lead CQV efforts for facilities and utilities, including HVAC, water systems, and building… more
- Actalent (Somerset, NJ)
- Job Title: CQV Engineer Job Description Assisting in development, review, and approval of cGMP documents including, but not limited to: Master Validation Plans, ... design documentation. Providing expertise and solutions to issues regarding CQV Lifecycle documentation in regards for applicable FDA/EMEA Regulations. Supporting… more
- Verista (New Brunswick, NJ)
- …our experiences to enhance our collective expertise Associate Project Engineer Responsibilities: + Manage validation documentation in automated systems, including ... test scripts, and validation reports. + Collaborate with the CQV and engineering teams to ensure documentation aligns with...test scripts, and validation reports. + Collaborate with the CQV and engineering teams to ensure documentation aligns with… more
- Verista (New Brunswick, NJ)
- …our experiences to enhance our collective expertise Lead CSV Engineer /Analyst Responsibilities: + Authoring, editing, and executing technical commissioning, ... for production equipment and analytical instruments. + Collaborate with engineering and CQV teams to align automation validation activities with project timelines. +… more