Job Description
Job Summary:
We are seeking an experienced and highly skilled Lead Validation Engineer to support validation, quality, engineering, and manufacturing programs within a cGMP-regulated biopharmaceutical environment.
The ideal candidate brings deep expertise in cleaning validation, equipment qualification, CQV, tech transfer support, and quality systems, along with the ability to lead cross-functional teams through complex validation and deviation resolution activities.
This role is responsible for authoring and executing validation protocols, driving investigations, ensuring site compliance, supporting regulatory inspections, and delivering high-quality documentation to enable the release and sustained performance of critical manufacturing and laboratory systems.
Roles & Responsibilities:
Validation & CQV Execution
Develop and execute validation strategies for cleaning processes, utilities, ...
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Job Details
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Location
Devens, Massachusetts
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Job Type
Full-time
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Category
Engineers
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Posted Date
June 07, 2026
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Application Deadline
July 17, 2026