Description
Job Advertisement: LCMS Bioanalytical Scientist
Position Overview:
I am currently partnered with a leading CRO which has an opening for an LCMS Bioanalytical Scientist to join their team and contribute to exciting drug research and development, as well as working in collaboration with industry leaders in the pharmaceutical sector. The suitable bioanalytical scientist will have the following responsibilities.
Key Responsibilities:
Develop and validate LCMS methods for regulated small molecule bioanalysis. Design and execute experiments to support drug development programs. Manage multiple projects simultaneously, ensuring timely delivery of high-quality data. Maintain compliance with GxP regulations and ensure all work adheres to industry standards. Collaborate with cross-functional teams to support client projects and internal initiatives. Prepare and review technical reports, protocols, and standard operating procedures (SOPs). Troubleshoot and optimize analytical methods and instrumentation.
Qualifications:
Ph.D. or M.Sc. in Analytical Chemistry, Biochemistry, or a related field. Minimum of 3-5 years of experience in LCMS method development and validation for bioanalysis. Proven track record in project management within a CRO or pharmaceutical environment. In-depth knowledge of GxP regulations and their application in bioanalytical laboratories. Strong problem-solving skills and the ability to work independently and as part of a team. Excellent communication and interpersonal skills.
What We Offer:
Competitive salary (£27,000– 32,000 Senior analyst / £32,000 - £37,000 Scientist / £37,000 - £42,000) Opportunities for professional development and career advancement. A collaborative and supportive work environment. Access to cutting-edge technology and resources.
How to Apply: Should you feel your experience aligns with the above apply and I will be in contact with you shortly.
Note: My client is unable to provide sponsorship for this position
