CQV Engineer
Katalyst CRO
South Plainfield, NJ
Contract
Mid Level
5+ years
Posted 1 month ago Expired
This job has expired
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Upload Your ResumeAbout This Role
Own equipment projects from concept to production in a highly regulated pharmaceutical environment, focusing on commissioning, qualification, and validation (CQV) activities.
Responsibilities
- Evaluate vendors, review quotes, and recommend equipment
- Lead commissioning, qualification, and validation (IQ/OQ)
- Develop SOPs, manage change control, and deliver equipment ready for GMP production
- Work directly with manufacturing and packaging equipment
- Review machine manuals and electrical drawings
- Drive small projects end-to-end as a technical CQV owner
Requirements
- 5+ years of CQV experience
- Hands-on equipment validation background
- Experience in pharma / biotech / regulated manufacturing
Qualifications
- 5+ years of CQV experience