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.

• 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.

• 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 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.

/OQ/PQ, Cell Therapy, GMP, FDA, Laboratory Equipment, Equipment Qualification, Data Integrity

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