Nexia is supporting an innovative UK-based pharmaceutical company focused on developing advanced therapies targeting immune-related conditions. With a strong R&D foundation and a growing pipeline, they are now looking to bring in a Mass Spectrometry expert to support the progression of analytical methods into a more regulated environment.
This is a great opportunity for someone who enjoys bridging early-stage research with GMP-ready processes, working cross-functionally to bring robust, high-quality methods into a controlled setting.
Key Responsibilities:
- Develop, optimise, and troubleshoot mass spectrometry-based identity assays
- Translate exploratory R&D methods into robust, qualification-ready analytical procedures
- Prepare high-quality documentation including method development reports, SOPs, and qualification protocols
- Collaborate across R&D, analytical development, and quality teams to support GMP readiness
- Provide technical expertise across instrumentation, sample preparation, analytical controls, and data integrity
What We’re Looking For:
- Strong experience in mass spectrometry within a life sciences setting
- Proven ability to move methods from R&D into regulated/GMP environments
- Solid understanding of analytical method development and validation principles
- Experience working cross-functionally in a collaborative environment
- Strong documentation skills with a focus on quality and compliance
If you’re looking for a role where you can make a real impact in shaping analytical processes within a growing and forward-thinking biotech, I’d love to share more.