Validation Engineer (CQV)

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

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