Analytical Development Chemist
On-siteHaverhill, England, United Kingdom
Job Summary
Develop, optimize, and pre-validate analytical methods for APIs, intermediates, raw materials, and drug product formulations using HPLC, UHPLC, GC, and hyphenated techniques like LC-MS and GC-MS. Support method transfers and troubleshooting across internal and client-facing projects while generating high-quality technical documentation including protocols and reports. Collaborate with cross-functional teams in R&D, Quality, and Manufacturing to integrate analytical methods into GMP workflows, maintaining compliance with cGMP, ICH guidelines, and internal quality systems. Utilize additional techniques such as FT-IR, UV-Vis, Karl Fischer, and NMR as appropriate. Join a growing, innovation-driven CDMO contributing to the development of life-changing medicines from early-stage research to commercial supply.
Required Qualifications
- BSc, MSc or Ph.D in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or a related discipline
- extensive industrial experience
- Proven experience in analytical method development
- experience within a pharmaceutical or CDMO environment
- Strong hands-on expertise with HPLC, UHPLC, and or GC instrumentation and software
- Familiarity with regulatory expectations for analytical methods used in API release testing
- Excellent problem-solving skills
- attention to detail
- collaborative mindset
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