Job Overview
Company
Katalyst HealthCares & Life Sciences
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Job Description
Responsibilities:
Execute validation activities across the full equipment lifecycle (FAT, SAT, Commissioning, DQ, IQ, OQ, PQ).
Apply GAMP methodology in a GMP-regulated environment.
Support Greenfield project initiatives and equipment startup.
Handle deviations, change controls, and validation deliverables.
Collaborate with cross-functional teams including QA, Engineering, and Manufacturing.
Requirements: Prior experience with fill-finish equipment including syringe assembly, serialization lines, and cartoners.
Strong understanding of GAMP and validation lifecycle documentation.
Hands-on exposure to Greenfield projects.
Excellent communication and documentation skills.
Experience managing deviations, CAPAs, and change controls.
About Katalyst HealthCares & Life Sciences
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