Sterile Process Validation Engineer — PPQ & Tech Transfer
Listed on 2026-10-11
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Engineering
Validation Engineer, Pharma Engineer, Quality Engineering
Katalyst CRO is seeking an experienced Process Validation Engineer for sterile pharmaceutical manufacturing projects in a GMP environment. The role emphasizes process validation, technology transfer, and PPQ execution for PFS lines.
You will collaborate with Manufacturing, Quality, Validation, and Engineering to deliver compliant projects, prepare protocols and reports, and ensure alignment with FDA/cGMP requirements throughout the validation lifecycle.
We invite applications for the Sterile Process Validation Engineer — PPQ & Tech Transfer position located in Newark, NJ, United States.
Full responsibilities and requirements are described in the listing above.
Learn more about the Sterile Process Validation Engineer — PPQ & Tech Transfer role in the description above.
We appreciate your interest in this position.
Join Katalyst CRO and contribute to our ongoing work.
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