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Process Validation Lead - Parenteral GMP Onsite

Job in Bloomington, Monroe County, Indiana, 47401, USA
Listing for: Simtra BioPharma Solutions
Full Time position
Listed on 2025-12-16
Job specializations:
  • Pharmaceutical
    Regulatory Compliance Specialist, Validation Engineer
Job Description & How to Apply Below
A Contract Development Manufacturing Organization is looking for a Process Validation Specialist to support compliance with regulatory requirements. This role includes developing procedures, performing validations, and collaborating with clients and teams. Candidates should possess a Bachelor's degree in a science or engineering field and have at least 5 years of technical experience in validation. This position offers comprehensive benefits and is 100% onsite in Bloomington, Indiana, with opportunities for growth and skill development.
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