Senior Validation Lead – CQV Sterile Injectables
Listed on 2026-10-06
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Healthcare
Healthcare Management -
Management
Healthcare Management
INCOG Bio Pharma Services in Fishers, IN is seeking a Senior Manager of Validation Engineering to lead CQV activities for utilities, equipment and related systems in a sterile injectables facility.
The role requires 10+ years in validation, 8+ years GMP or regulated industry experience, and at least 5 years of supervisory leadership. Onsite work is required, with opportunities to influence capital projects and regulatory interactions.
The following opportunity is for a Senior Validation Lead – CQV for Sterile Injectables with INCOG Bio Pharma Services.
Step into the Senior Validation Lead – CQV for Sterile Injectables role at INCOG Bio Pharma Services in Fishers, IN, United States and grow with us.
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