Pharma CQV Validation Engineer - Bloomington, IN
Verista, Inc.
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Benefits offered by this job
Job summary
Verista is seeking a Validation Engineer for the Bloomington, IN area to ensure quality and regulatory compliance in pharmaceutical processes. The role focuses on equipment qualification and process validation to safeguard patient safety and product integrity.
Ideal candidates have 3+ years in validation engineering within pharma/biotech, with hands-on experience in GMP environments and utilities/HVAC considerations.
Qualifications
- 3+ years in validation engineering within pharmaceuticals or biotech.
Skills
Job description
Verista is seeking a Validation Engineer for the Bloomington, IN area to ensure quality and regulatory compliance in pharmaceutical processes. The role focuses on equipment qualification and process validation to safeguard patient safety and product integrity.
Ideal candidates have 3+ years in validation engineering within pharma/biotech, with hands-on experience in GMP environments and utilities/HVAC considerations.
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