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Posted 05 August, 2026

Senior QC Scientist

SRG
Greater Manchester, ENG, GB Full Time

Job Description

Senior QC Scientist

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Greater Manchester

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SRG 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.

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Due 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.

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Key Responsibilities

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  • Perform analytical testing including:
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  • HPL / UHPLC (Assay, Related substances & Cleaning verification methods)
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  • Dissolution Testing inc. method transfers, validations and troubleshooting.
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  • Compendial techniques – FTIR, pH, content uniformity, water content etc.
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  • Ensure compliance with GMP and regulatory standards, supporting audit and inspection readiness
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  • Write and review:
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  • Analytical methods and validation documentation
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  • SOPs and laboratory quality documents
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  • Certificates of Analysis and technical reports
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  • Manage stability studies from initiation through to reporting, including third-party liaison
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  • Support onboarding and lifecycle management of QC instrumentation (IQ/OQ/PQ)
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  • Supervise and mentor junior scientists, including training and competency sign-off
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  • Contribute to continuous improvement initiatives, including lean QC processes
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  • Support QC planning, laboratory organisation, and resource allocation
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Required

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  • A degree or comparable experience in Chemistry, Pharmaceutical Sciences, Biochemistry, or similar relevant field.
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  • Proven QC / analytical experience within a similar GMP environment.
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  • Skilled in the operation of HPLC / UHPLC, FTIR and similar techniques.
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  • Experience with method validation, transfer, and technical documentation
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  • Good understanding of regulatory frameworks (e.g. EU GMP, ICH guidelines)
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  • Exposure to stability studies and data trending would be advantageous
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  • Previous experience mentoring or supervising colleagues is desirable
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