Piper Companies is currently seeking a Validation Manager based in Lynwood, California for work at a pharmaceutical development and manufacturing company.
The Engineer will ensure the proper implementation of manufacturing equipment and computerized systems.
This position will be on-site.
Responsibilities of the Engineer :
- 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
Qualifications of the Engineer :
- 6+ years experience in FDA-regulated industry performing IQ / OQ / PQ functions or writing protocols / URS
- 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
Compensation for the Engineer :
- $120,000 salary; full-time
- Comprehensive Benefits package : Medical, Dental, Vision, 401K, PTO
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