Validation Engineer (CQV)

Piper Companies; Raritan (NJ); On-site; USD 55,000 - 62,000; Full time

Benefits offered by this job

Medical benefits

Dental benefits

Vision benefits

401(k)

Sick leave

Paid holidays

Job summary

Piper Companies is seeking a Validation Engineer (CQV) in Raritan, NJ to support a leading cell therapy organization. This role focuses on commissioning, qualification, and validation of laboratory equipment within a GMP-regulated cell therapy environment.

Responsibilities include IQ/OQ/PQ execution, CQV documentation, and ensuring equipment readiness while maintaining data integrity and regulatory alignment. This onsite, long-term contract position offers comprehensive benefits and on-site work.

Qualifications

• Experience in pharmaceutical/bi biotech or cell therapy environments is required.
• Hands-on equipment qualification and validation experience.
• Familiarity with CQV, GMP, and IQ/OQ/PQ processes.

Responsibilities

• Execute IQ/OQ/PQ for laboratory equipment and instrumentation.
• Develop and maintain CQV documentation (URS, protocols, reports).
• Ensure data integrity and GMP compliance.
• Collaborate with QC, QA, Engineering, and vendors to ensure equipment readiness.

Skills

CQV knowledge

GMP knowledge

IQ/OQ/PQ experience

Data integrity awareness

Education

Bachelor's degree in Engineering, Life Sciences, or related field

Job description

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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