GMP QA Associate - Cell Therapy

Autolus-Ltd-; Stevenage; On-site; GBP 28,000 - 52,000; Full time

Job summary

Autolus is a biopharmaceutical company advancing next-generation CAR T therapies. Based in Stevenage, the QA Associate will support Good Manufacturing Practice in a multi-product facility and help ensure batch release and documentation integrity.

You will collaborate with QA and production teams across sites, contribute to audit readiness, and support continuous improvement of the Pharmaceutical Quality System while maintaining safety and compliance.

Qualifications

• Experience working with GMP systems and controlled documentation.
• Meet requirements to work in a cleanroom environment.
• Higher education: BSc in pharmaceutical services, immunology, biology, chemistry or relevant discipline.

Responsibilities

• Maintaining Good Manufacturing Practice in a multi-product facility.
• Interact with functions to ensure cGMP for batch release activities.
• Review Batch Manufacturing Records and QC records for issues.
• Prepare and check in-process and Drug Product labels for traceability.
• Identify compliance risks and recommend improvements.

Skills

Good communications

Attention to detail

Accurate data entry

Prioritisation

Reliability

Teamwork

Education

BSc in pharmaceutical sciences

Job description

Autolus is a biopharmaceutical company advancing next-generation CAR T therapies. Based in Stevenage, the QA Associate will support Good Manufacturing Practice in a multi-product facility and help ensure batch release and documentation integrity.

You will collaborate with QA and production teams across sites, contribute to audit readiness, and support continuous improvement of the Pharmaceutical Quality System while maintaining safety and compliance.