Posted 05 August, 2026
Senior QC Scientist
SRG
Greater Manchester, ENG, GB
Full Time
Job Description
Senior QC Scientist
\nGreater Manchester
\nSRG are recruiting for a Senior QC Scientist to join a highly successful CDMO based in Greater Manchester. Growing rapidly, the business specialises in taking products from discovery, all the way through early-stage trials and to approval.
\nDue to continued growth and expansion of the business they are seeking to hire a Senior QC Scientist to join their team in Greater Manchester to lead hands on QC testing, ensure the GMP compliance of finished products and support ongoing development & continuous improvement of QC Systems, methods and regulatory readiness.
\nKey Responsibilities
\n- \n
- Perform analytical testing including: \n
- HPL / UHPLC (Assay, Related substances & Cleaning verification methods) \n
- Dissolution Testing inc. method transfers, validations and troubleshooting. \n
- Compendial techniques – FTIR, pH, content uniformity, water content etc. \n
- Ensure compliance with GMP and regulatory standards, supporting audit and inspection readiness \n
- Write and review: \n
- Analytical methods and validation documentation \n
- SOPs and laboratory quality documents \n
- Certificates of Analysis and technical reports \n
- Manage stability studies from initiation through to reporting, including third-party liaison \n
- Support onboarding and lifecycle management of QC instrumentation (IQ/OQ/PQ) \n
- Supervise and mentor junior scientists, including training and competency sign-off \n
- Contribute to continuous improvement initiatives, including lean QC processes \n
- Support QC planning, laboratory organisation, and resource allocation \n
Required
\n- \n
- A degree or comparable experience in Chemistry, Pharmaceutical Sciences, Biochemistry, or similar relevant field. \n
- Proven QC / analytical experience within a similar GMP environment. \n
- Skilled in the operation of HPLC / UHPLC, FTIR and similar techniques. \n
- Experience with method validation, transfer, and technical documentation \n
- Good understanding of regulatory frameworks (e.g. EU GMP, ICH guidelines) \n
- Exposure to stability studies and data trending would be advantageous \n
- Previous experience mentoring or supervising colleagues is desirable \n
