CQV Validation Engineer - Cell Therapy (Onsite, Long-Term)

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 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.