We’re supporting the growth of a new specialist QC function within a dynamic, multi-site pharmaceutical operation across the UK. This is a project-focused role working alongside a dedicated validation team, supporting new product introductions, method development, and technical transfer across multiple UK sites.
You’ll play a key role in bringing new methods into GMP QC environments, scaling processes, and embedding robust validation practices across the network.
What you need to know
* Multi-site role – based out of a North UK facility but with travel required across all UK sites
* Working closely with a central validation team, while remaining part of the wider QC function
* Reporting line into QC leadership, with strong project-based collaboration
* Focus on new product introduction, validation and tech transfer before handover to local QC teams
* Core responsibilities include:
* Method validation and transfer (some method development)
* Scaling up analytical methods for routine QC use
* Training QC teams on validated methods
What you need to bring
* 2–3 years’ experience in a GMP QC or analytical environment
* Demonstrated expertise in analytical method validation – not just some exposure, but independent troubleshooting and problem solving
* Hands-on experience with HPLC and GC techniques
* Strong understanding of GMP requirements within a regulated setting
* Experience supporting method development, optimisation, or tech transfer
* Ability to work in a project-driven, multi-site environment
* Confident communicator, capable of training and supporting QC teams during method handover
QC, control, quality, analytical, chemist, method, validation, HPLC, chromatography, GC, transfer, scale, tech, manufacturing, development, validate, wet, TLC, bench
Salary description
£38000.00 - £45000.00 per year