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.
#J-18808-LjbffrSenior CQV Engineer - Pharma Validation Leader in bloomington at Unknown Company
This position is listed as full time and onsite.