Piper Companies
Quality Assurance Specialist (Cell Therapy)
Piper Companies, Branchburg Township, New Jersey, United States
Overview
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
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–$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.
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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
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–$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.
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