QA Specialist Consultant

Piper Companies is seeking a Quality Assurance Specialist to support GMP manufacturing operations for a leading biotechnology company developing next-generation allogeneic cell therapies for oncology.

This is an onsite position in Branchburg, NJ and a long term contract assignment with potential for conversion.

Responsibilities:

• Support GMP manufacturing and clinical operations through documentation control and quality oversight.
• Review executed batch records and resolve discrepancies with manufacturing teams.
• Manage issuance, routing, and archiving of quality records and controlled documents.
• Perform QA review and release of incoming raw materials.
• Revise SOPs, protocols, and reports as needed to maintain compliance.

Qualifications:

• 2–4 years of QA experience in a GMP-regulated biopharma or cell/gene therapy environment.
• Strong understanding of cGMP requirements and documentation practices.
• Excellent attention to detail and ability to communicate effectively across teams.
• Team-oriented, proactive, and able to work in a fast-paced environment.
• BS or MS in a biological, technical, or engineering discipline.

Compensation:

• Pay Rate: $40–$45/hour, depending on experience
• Benefits Available: Medical, Dental, Vision, Sick Leave as required by law, and

This job opens for applications on 12/15/2025. Applications for this job will be accepted for at least 30 days from the posting date.  

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