About the role

Simtra US LLC in Bloomington, IN seeks a CQV Principal Engineer to lead commissioning, qualification and validation for pharma manufacturing equipment. You will author and review documentation, manage CAPAs, and mentor engineers across teams. Cross-functional collaboration with Quality, EHS, Maintenance and Manufacturing is essential; this is a 100% onsite role requiring a BS in engineering or life sciences and 10+ years in pharma/biotech. Strong communication and project skills are required.

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JOB OVERVIEW

Experience level

Manager

Location

Bloomington, IN

Occupation

Validation Engineers

Industry

Pharmaceutical Preparation Manufacturing

Posted

today

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