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CMC Lead - Cell & Gene Therapy
Posted 9 days 22 hours ago by Barrington James Limited
We are partnering with a rapidly growing, innovation-led biotechnology organisation focused on advancing next-generation cell and gene therapies. With a strong pipeline and significant investment into viral vector platforms, the business is now looking to appoint a CMC Lead to play a critical role in driving development from early-stage through to commercialisation.
This is a high-impact position offering the opportunity to shape CMC strategy, lead cross-functional programs, and work at the forefront of AAV and lentiviral vector development.
The RoleAs CMC Lead, you will take ownership of the Chemistry, Manufacturing & Controls (CMC) strategy across multiple programs, ensuring robust development, scalability, and regulatory alignment.
You will act as a key interface between technical, regulatory, and manufacturing teams, driving progress across development stages and ensuring successful delivery of key milestones.
Key Responsibilities- Lead and define CMC strategy for viral vector-based therapies (AAV / Lentiviral)
- Oversee process development, scale-up, and tech transfer into GMP manufacturing
- Collaborate with MSAT, manufacturing, quality, and regulatory teams to ensure alignment
- Support and contribute to regulatory submissions (IND, IMPD, BLA)
- Manage external CDMOs and development partners
- Drive process optimisation, robustness, and scalability
- Ensure compliance with GMP standards and regulatory expectations
- Provide technical leadership across cross-functional project teams
- Strong experience in CMC development within cell & gene therapy or biologics
- Proven expertise in viral vectors (AAV, Lentiviral preferred)
- Background in upstream process development, bioprocessing, or related field
- Experience with tech transfer, process scale-up, and GMP manufacturing
- Understanding of regulatory requirements and CMC documentation
- Demonstrated ability to lead cross-functional teams and manage complex programs
- Experience working with or managing CDMOs
- Exposure to process validation and commercial manufacturing readiness
- Advanced degree (PhD or equivalent) in a relevant scientific discipline
Barrington James Limited
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