The client is seeking a candidate with a strong background in pharmaceutical and biopharmaceutical analysis.

Key responsibilities:

• Performing complex sample preparation and analysis, troubleshooting instrumentation issues, and maintaining compliance with GMP/GLP standards.
• The candidate will manage QC/QA tasks, interpret and analyze data for accuracy, and communicate project updates effectively.
• They should plan and document laboratory experiments, maintain mammalian cell cultures, and support antibody discovery.
• A Bachelor's or Master's degree in a relevant scientific field and 2+ years of experience are required.
• The candidate must have knowledge of regulatory guidelines, GMP/GLP practices, and proficiency in Microsoft Excel and Word. Skills in time management, problem-solving, and collaboration are essential. Experience with liquid handling automation is a plus.

This is a first-shift, Monday-Friday.