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- Responsible for ownership of all lifecycle deliverables in the qualification of equipment and multi-user computerized systems
- Supports internal customer groups in the procurement, operation, calibration, and preventive maintenance of equipment
- Supervises vendors for qualification functions
- 5+ years experience in FDA-regulated industry performing IQ/OQ/PQ
- Experience with HPLC/other lab equipment
- Excellent understanding of cGXP requirements and good documentation practices relating to systems, equipment and instrumentation within the pharmaceutical industry
- Working knowledge of ISPE guidance and 21 CFR Part 11 compliance
- BS in Engineering/Science or equivalent
- $50+ hr
- Comprehensive Benefits package: Medical, Dental, Vision, 401K, PTO
- ID: #49540240
- State: New Jersey Titusville 08560 Titusville USA
- City: Titusville
- Salary: USD TBD TBD
- Job type: Permanent
- Showed: 2023-03-25
- Deadline: 2023-05-23
- Category: Architect/engineer/CAD