Process Validation Specialist III – Parenteral Manufacturing
Job in
Bloomington, Monroe County, Indiana, 47401, USA
Listed on 2026-07-18
Listing for:
Simtra US LLC
Full Time
position Listed on 2026-07-18
Job specializations:
-
Quality Assurance - QA/QC
Regulatory Compliance Specialist, Quality Engineering
Job Description & How to Apply Below
Simtra US LLC is seeking a Process Validation professional in Indiana to execute validation activities for parenteral products. You will develop protocols, analyze data, and ensure compliance with global regulations. You will interact with cross‑functional teams and clients and report to the Process Validation Sr.
Manager. You should have at least 5 years in process validation, strong statistics skills, and experience with GMP environments.
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