Scientist - Method Development

Associate Scientist - Method Development Essential ResponsibilitiesPerform routine HPLC and GC analysis in a GMP analytical laboratoryMay also perform MS, FTIR, NMR, MS, KF, XRD, DSC, TGA, and other analysesCoordinate stability testing, write protocols and reportsCoordinate the timely and compliant generation of data to support client projectsReview data for technical content and good record keeping practicesOther duties as assignedRequirements Educational QualificationsMinimum 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 RequirementsExperience with HPLC equipment and analysisExperience with FTIR, GC, NMR, MS, KF, XRD, DSC, TGA, desired but not requiredExperience with standard lab equipment (balances, pipettes, pH meter, etc.)Proficient in Microsoft Excel and WordMust have basic chemical knowledge and be able to handle materials safelyMust be able to communicate effectively with manufacturing and quality personnel.

Must be able to effectively multitask.