I’m working with an innovative pharma company looking for a Mass Spectrometry Expert to play a key role in translating early-stage science into GMP-ready analytical methods.
This is a great fit for someone who enjoys the detail method development, problem solving, and turning exploratory work into something robust, reproducible, and inspection-ready.
What you’ll be doing:
* Developing, optimising, and troubleshooting MS-based identity assays
* Translating R&D methods into controlled, qualification-ready procedures
* Writing high-quality documentation (SOPs, method development reports, qualification protocols)
* Collaborating across R&D, Analytical Development, and Quality to support GMP readiness
* Providing technical input on instrumentation, sample prep, analytical controls, and data integrity
What they’re looking for:
* Strong experience in mass spectrometry method development
* Someone comfortable working across both R&D and regulated/GMP environments
* Detail-oriented, with a focus on documentation and quality standards
* A collaborative mindset this role sits right at the interface of multiple teams
This is a brilliant opportunity for someone who wants to own the transition from discovery into a regulated setting and have real impact on how methods are built and scaled.