Sr Associate II Method Validation - Indianapolis IN

The Sr Associate II Method Validation position involves developing and validating analytical methods for parenteral radiopharmaceutical products, participating in method transfer activities, and ensuring accuracy and reliability of data. The role requires strong knowledge of analytical techniques and GMP regulations, as well as excellent communication and problem-solving skills.

Requirements

• B.Sc. or M.Sc. in Analytical Chemistry, Pharmaceutical Sciences, or relevant scientific field
• Three (3) or more years of pharmaceutical industry experience
• Strong knowledge of analytical techniques such as UHPLC, HPLC, GC, TLC, ICP, LC-MS, Gamma Spectrometry, Alpha Spectrometry, and other analytical methods
• Knowledge of GMP regulations, quality systems, and safety guidelines

Benefits

• Health insurance
• 401(k) matching
• Paid time off