Biopharma Validation Engineer - GMP IQ/OQ/PQ Focus
Job in
Boston, Suffolk County, Massachusetts, 02298, USA
Listed on 2026-07-18
Listing for:
BioSpace
Full Time
position Listed on 2026-07-18
Job specializations:
-
Quality Assurance - QA/QC
Quality Engineering, Regulatory Compliance Specialist -
Engineering
Quality Engineering, Biomedical Engineer, Pharma Engineer, Regulatory Compliance Specialist
Job Description & How to Apply Below
Syner-G is seeking a Validation Engineer to develop and execute validation protocols for multiple processes. You will drive quality performance and regulatory compliance by defining and maintaining the validation program across the organization.
The role requires a bachelor’s in a life science and 3–10 years in biotech/pharma/medical devices with FDA cGMP, FMEA, and risk analysis exposure. Candidates should be skilled in writing IQ/OQ/PQ documents and related reports.
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