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