Piper Companies is seeking a Validation Engineer (CQV) in Raritan, NJ to support a leading cell therapy organization . This role focuses on the commissioning, qualification, and validation of laboratory equipment within a GMP-regulated cell therapy environment.
Responsibilities for the Validation Engineer (CQV):
- Execute IQ/OQ/PQ for laboratory equipment and instrumentation.
- Develop and maintain CQV documentation, including URS, protocols, and reports.
- Ensure equipment qualification and data integrity meet GMP and FDA standards.
- Support equipment installation, lifecycle management, and periodic reviews.
- Draft and update SOPs, calibration procedures, and work instructions.
- Collaborate with QC, QA, Engineering, and vendors to ensure equipment readiness.
Qualifications for the Validation Engineer (CQV):
- Bachelor’s degree in Engineering, Life Sciences, or a related field.
- 3+ years of pharmaceutical, biotechnology, or cell therapy experience.
- Hands‑on experience with equipment qualification and validation.
- Strong knowledge of CQV, GMP, and IQ/OQ/PQ requirements.
- Experience writing and reviewing SOPs, protocols, and qualification reports.
Compensation for the Validation Engineer (CQV):
- Pay Rate: $40–45/hr
- Location: Raritan, NJ – Onsite
- Type: Long-Term Contract
- Comprehensive Benefits: Medical, Dental, Vision, 401(k), Sick Leave (as required by law), and Paid Holidays
Application Period: Opens 8/7/2026 and remains open for at least 30 days.
Keywords: CQV, Commissioning, Qualification, Validation, IQ/OQ/PQ, Cell Therapy, GMP, FDA, Laboratory Equipment, Equipment Qualification, Data Integrity
#LI-JM1 #LI-ONSITE
#J-18808-Ljbffr