Our client is a large pharma company at the forefront of innovation in the pharmaceutical industry, committed to improving global health through groundbreaking research and development. Their team is dedicated to the advancement of protein-based vaccines, striving to make a difference in the lives of millions. They are seeking a skilled and motivated Associate Scientist to join our Bioanalytical team with a focus on Liquid Chromatography-Mass Spectrometry (LCMS).

Job Description:

As an Associate Scientist in Bioanalytical Development specializing in LCMS, you will play a crucial role in advancing our analytical capabilities for the characterization of complex biological products. You will develop and implement robust LCMS-based methods to support the development, validation, and transfer of assays essential for our therapeutic pipeline.

Key Responsibilities:

• Develop, optimize, and validate LCMS methods for the analysis of protein-based therapeutics and other complex biomolecules.
• Perform routine and advanced LCMS assays, ensuring accurate and reliable results.
• Analyze and interpret LCMS data to support product characterization, stability studies, and quality control.
• Collaborate with cross-functional teams to integrate LCMS methodologies into the broader analytical and development framework.
• Document experimental procedures, results, and findings in compliance with cGMP and regulatory standards.
• Troubleshoot and resolve technical issues related to LCMS instrumentation and methodologies.
• Participate in the technology transfer of LCMS methods to Quality Control and manufacturing teams.
• Stay current with advancements in LCMS technology and regulatory guidelines.

Qualifications:

• Bachelor's or Master's degree in Analytical Chemistry, Biochemistry, Biotechnology, or a related field.
• 2 years of experience in analytical development with a focus on LCMS.
• Proficiency in LCMS techniques and data analysis, with hands-on experience in method development and validation.
• Strong analytical and problem-solving skills with attention to detail.
• Excellent documentation and communication skills.
• Ability to work effectively in a collaborative, team-oriented environment.
• Knowledge of regulatory requirements and quality standards in the pharmaceutical industry.

Full job description and company details available upon application. This position is managed by Sam Long at Meet Recruitment. Email sam.long@peoplewithchemistry.com to discuss the position further.