Associate Scientist - Method Development

Essential Responsibilities

• Perform routine HPLC and GC analysis in a GMP analytical laboratory
• May also perform MS, FTIR, NMR, MS, KF, XRD, DSC, TGA, and other analyses
• Coordinate stability testing, write protocols and reports
• Coordinate the timely and compliant generation of data to support client projects
• Review data for technical content and good record keeping practices
• Other duties as assigned

Requirements Educational Qualifications

Minimum B.S. in chemistry with 5+ years related pharmaceutical analytical laboratory experience or equivalent combination of education and experience is required. Relevant experience in good laboratory/manufacturing practices (GLP/cGMP), laboratory quality control or stability, and interaction with quality assurance is desired.

Specific Skills and Requirements

• Experience with HPLC equipment and analysis
• Experience with FTIR, GC, NMR, MS, KF, XRD, DSC, TGA, desired but not required
• Experience with standard lab equipment (balances, pipettes, pH meter, etc.)
• Proficient in Microsoft Excel and Word
• Must have basic chemical knowledge and be able to handle materials safely
• Must be able to communicate effectively with manufacturing and quality personnel.
• Must be able to effectively multitask.