About this opportunity
Simtra BioPharma Solutions lists this Senior CQV Engineer - Pharma Validation Leader opportunity in bloomington, Indiana. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Simtra BioPharma Solutions in Bloomington, Indiana seeks a Commissioning, Qualification, and Validation (CQV) Principal Engineer to define and maintain engineering documentation and life cycle management practices for CQV within pharma manufacturing.
The role collaborates with Quality, EHS, Maintenance and Manufacturing, reports to the Director of Engineering, and is 100% onsite at the Bloomington facility. Strong leadership and regulatory experience are required.
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Worksite address
bloomington, IN, 47401, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.