Senior Method Development Scientist - Bioanalysis

Job Overview:

Do you have Bioanalysis method development experience and are currently looking for your next challenge?

Would you like to work for the World's leading drug development organisation?

Our largest UK site in Harrogate, North Yorkshire is currently recruiting for a Method Development Specialist to join our Small Molecule team within the Bioanalysis division. The Bioanalysis division is responsible for providing analytical testing services to key pharmaceutical and biotech clients to support toxicology, safety assessment and clinical studies.

As the Method Development Scientist, you will be responsible for the development of quantitative LCMS methods in accordance with client specifications and regulatory requirements. Methods produced will be validated and provided to the operational team, so they can perform client sample analysis. Serve as the primary point of contact for scientific & regulatory requirements for method development working closely with Study Directors and other Responsible analysts to ensure that client expectations are met Liaise and act as the first point of contact for clients, actively working to develop assays in accordance with client requirements Actively collaborate with the bioanalysis team to ensure the clients’ studies are completed to the highest possible standard Promote a positive impression of Covance internally and within the industry. Proactively identify ways to increase client satisfaction

What Covance can offer you: Competitive salaries and a comprehensive benefits package including health cover and contributory pension Unrivalled opportunities to develop a successful career in the scientific industry Unsurpassed career development opportunities Ability to work with a variety of different clients on wide ranging projects Education/Qualifications:Scientific Degree - BSc, MSc/PhD or equivalent Experience:Must have laboratory experience with experience developing LCMS assays within the scientific industry In depth e xperience using LCMS Experience working in a GLP/GCP regulated environement, with an understanding of regulatory requirements for Bioanalysis studies Experience working in the Pharmaceutical or CRO industry is preffered but not essential Excellent communication and interpersonal skills Proven ability to prioritize and manage time , with e xcellent attention to detail A bility to utilize word processing, database, spreadsheet, and specialized software