About this opportunity
CAI lists this Lead CQV Validation Engineer — GMP & Compliance opportunity in bloomington, Indiana. Review the employer’s description below for duties, qualifications and application requirements.
Job description
A leading life sciences firm is seeking a professional focused on Commissioning, Qualification, and Validation (CQV) execution with a strong safety emphasis. Candidates should possess a Bachelor's degree in Engineering, Chemistry, or Life Sciences and have over three years of relevant experience in the Pharmaceutical/Life Sciences industry. Key responsibilities include project planning, documentation compliance, and vendor management. The role requires excellent communication skills and the ability to travel across the U.S. and possibly internationally. Benefits include comprehensive health coverage and a generous PTO policy.
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Worksite address
bloomington, IN, 47401, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.