Validation Engineering Leader – Sterile Injectables
Listed on 2026-10-06
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Engineering
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Management
INCOG Bio Pharma in Fishers, IN seeks a Senior Manager of Validation Engineering to lead CQV activities for sterile injectables manufacturing and packaging. You will partner with internal and external customers to meet client project needs, capital expansion initiatives, and maintain validated state, influencing outcomes across the organization.
The role requires 10+ years in Validation with 8+ years GMP experience, plus 5+ years of supervision, and is onsite at our Fishers campus.
This posting is for the Validation Engineering Leader – Sterile Injectables role at INCOG Bio Pharma, based in Fishers, IN, United States.
Full responsibilities and requirements are described in the listing above.
Learn more about the Validation Engineering Leader – Sterile Injectables role in the description above.
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