Senior Process Validation Specialist — GMP & CPV Expert
Job in
Bloomington, Monroe County, Indiana, 47401, USA
Listed on 2026-07-17
Listing for:
Simtra-Biopharma-Solutions
Full Time
position Listed on 2026-07-17
Job specializations:
-
Pharmaceutical
Quality Engineering, Regulatory Compliance Specialist, Validation Engineer
Job Description & How to Apply Below
Simtra-Biopharma-Solutions seeks a Process Validation professional to execute validation activities across parenteral manufacturing, ensuring adherence to global regulatory standards and internal best practices. You will collaborate with clients and internal teams to define scope, write protocols, and analyze technical data, supporting CPV and audit-ready documentation.
Applicants should have a BS in science/engineering and 5+ years of validation experience, with strong communication and
#J-18808-LjbffrPosition Requirements
10+ Years
work experience
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