Research Associate

A global pharmaceutical organisation is seeking a Research Associate (contract) with deep expertise in analytical method development and validation. This is an opportunity to support vital healthcare innovation in a fast-paced, regulated environment. The contract offers the chance to contribute to projects that directly impact product quality and patient safety, while working alongside cross-functional teams of technical experts.

This is a highly specialised role for someone who enjoys translating complex data into practical outcomes, applying critical thinking to scientific problems, and operating with independence. Working within a collaborative R&D environment, the successful contractor will help ensure the performance and compliance of analytical methods across the development lifecycle.

Your role as Research Associate:

• Lead the development and validation of analytical methods, using statistical and scientific principles to ensure robust, fit-for-purpose results

• Evaluate and recommend suitable techniques to meet defined analytical targets, drawing on deep expertise in chromatographic and compendial methods

• Interpret complex experimental data to guide method optimisation, sharing insights through clear, evidence-based reports and presentations

• Collaborate with internal teams and external CROs on method transfer, validation, and lifecycle management activities

• Support resolution of technical challenges, offering practical solutions to maintain project timelines and quality standards

• Document all activity in line with Good Documentation Practices (GDP) and relevant quality systems

Experience and qualifications for the Research Associate role:

• Master's degree in Analytical Chemistry, Pharmaceutical Sciences, or a related field

• 5-10 years of hands-on experience in method development and validation within a pharmaceutical or biotech environment

• Expert knowledge of chromatography (HPLC, GC) and supporting techniques such as UV, Karl Fischer, and titration

• Strong understanding of regulatory expectations (e.g., ICH, GMP) and analytical quality guidelines

• Confident in cross-functional communication and problem-solving, with a mindset focused on continuous improvement

• Experience contributing to method lifecycle management, including transfer, troubleshooting, and comparability studies

For immediate consideration, please apply today. If this role isn't quite right, but you're interested in contract opportunities within pharmaceutical R&D or analytical sciences, get in touch to hear about other roles in the sector.