GMP QA Associate - Cell Therapy (Stevenage)

Autolus, Inc.; Stevenage; Remote; GBP 28,000 - 40,000; Full time

Benefits offered by this job

Private medical insurance

Life insurance

Pension

Employee share scheme

Flexible working

Job summary

Autolus, Inc. in Stevenage is seeking a QA Associate to join the QA Operations team. The role reports to the QA Manager/Senior QA Specialist and involves working in a multi-product GMP facility, supporting batch release, documentation, and regulatory compliance for autologous CAR-T products.

You will interact with cross-functional teams, maintain cGMP, ensure traceability, and contribute to continuous improvement of the PQS while supporting inspection readiness and safety policies.

Qualifications

• Experience with GMP systems and controlled documentation.
• Cleanroom environment requirement.
• Bachelor-level degree in pharmaceutical sciences or related field.

Responsibilities

• Maintain GMP compliance in QA operations to support batch release.
• Review documentation to ensure traceability and regulatory compliance.
• Support inspection readiness activities and audits.
• Collaborate with QA team to investigate quality events and root causes.

Skills

GMP systems

Cleanroom

Communications

Attention to detail

Data entry

Time management

Team player

Education

BSc in pharmaceutical sciences or related field

Job description

Autolus, Inc. in Stevenage is seeking a QA Associate to join the QA Operations team. The role reports to the QA Manager/Senior QA Specialist and involves working in a multi-product GMP facility, supporting batch release, documentation, and regulatory compliance for autologous CAR-T products.

You will interact with cross-functional teams, maintain cGMP, ensure traceability, and contribute to continuous improvement of the PQS while supporting inspection readiness and safety policies.