Method Development Associate Scientist

Our client is a contract research and development manufacturing service provider to chemical-based industries, and they’re looking for a Method Development Associate Scientist to join their growing team!

Pay: Up to 100k based on experience

Location: Concord, OH

Schedule: M-Friday 8-5

Responsibilities:

• Develop and validate HPLC and GC procedures for small molecule drug substances and drug products.
• Perform forced degradation studies and develop stability-indicating assay and impurities methods
• Work in a GLP/GMP laboratory. Coordinate the timely and compliant generation of data to support client projects.
• Perform routine HPLC, GC, NMR, MS, IR, ICP, KF and other analysis and validation studies.
• Author and review protocols and reports. Review data for technical content and accuracy.
• Maintain current expertise with relevant ICH, GMP, and FDA guidelines.

Specific Skills:

• Experience in standard lab instrumentation (HPLC, UPLC, etc.)
• Experience with LCMS and GC preferred but not required.

Qualifications:

• B.S. to Ph.D. in chemistry or related field with 5+ years analytical laboratory experience or equivalent combination of education and experience is required.
• Relevant experience in good manufacturing practices (GMP) laboratory is required.