Quality Assurance Specialist (Cell Therapy)

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. The organization focuses on creating scalable, off-the-shelf immunotherapies that improve accessibility and transform patient outcomes. The role is located in Branchburg, NJ.

Responsibilities of the Quality Assurance Operations Specialist:

• 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 of the Quality Assurance Operations Specialist:

• 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 for the Quality Assurance Operations Specialist:

• Pay Rate: $40–$48/hour (based on experience)
• Long-term contract with strong potential to extend
• Onsite role in Branchburg, NJ

Application Period: This position opens for applications on 10/10/2025 and will remain open for a minimum of 30 days from the posting date.

Keywords: Quality Assurance, QA Specialist, GMP, Biologics, Cell Therapy, Gene Therapy, Batch Record Review, Document Control, Raw Material Release, SOP, Quality Systems, Manufacturing Support, iPSC, Branchburg NJ

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