CQV Validation Lead – Biologics GMP Restart
Listed on 2026-10-06
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Quality Assurance - QA/QC
Regulatory Compliance Specialist
Barrington James is seeking an experienced CQV Engineer to support a GMP facility restart within a biologics manufacturing environment. This role involves leading CQV activities for process equipment and ensuring compliance with GMP standards.
Ideal candidates will have 5-7 years of experience in validation, particularly within pharma or biotech sectors. Strong technical writing and an understanding of Annex 11 requirements are necessary. This position offers a dynamic and project-driven work environment.
This opportunity is for the CQV Validation Lead – Biologics GMP Restart role at Barrington James.
The position is based in Boston, MA, United States.
This opportunity is part of our work in Engineering.
The advertised compensation is 90..
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
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