Walker Cole International is supporting a pharmaceutical organisation based in Central London in the search for an QA Consultant to support core quality operations within a regulated environment.
This role will focus on day-to-day QA activities, ensuring compliance with GxP standards and supporting manufacturing and quality systems. We are particularly interested in candidates with experience in cell and gene therapy, biotechnology, or sterile environments.
Key Responsibilities
- Support and verify deviations, working closely with departments to ensure timely resolution
- Review and support master batch documentation (BPR/BRR), including issuance and oversight
- Contribute to Product Quality Report (PQR) preparation
- Prepare and deliver training materials to support quality processes
- Assign and manage material status for production activities
- Write, review, and manage Quality System documentation (e.g. SOPs, policies, records)
- Ensure compliance with GxP standards and support inspection readiness (e.g. MHRA)
Required Experience & Skills
- Proven QA experience within pharmaceutical, biotech, or life sciences environments
- Background in cell & gene therapy, biologics, or sterile manufacturing is highly desirable
- Strong hands-on experience with deviations, batch records, and QMS documentation
- Good understanding of GxP regulations and quality systems
- Experience supporting manufacturing QA activities
- Strong attention to detail and ability to work cross-functionally
Contract Details
- Location: London (on-site)
- Length: 12 months
- Rate: Competitive day rate (DOE)
Contact
fk@walkercole.com
0208 103 5472