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

• 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.

Requirements

• 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.

Pay

$40–45/hr

Schedule

Long-Term Contract, Onsite (Raritan, NJ)

Benefits

• Medical, Dental, Vision
• 401(k)
• Sick Leave (as required by law)
• Paid Holidays