Onsite CQV Engineer - GMP Validation Specialist
Listed on 2026-10-02
-
Engineering
Pharma Engineer, Quality Engineering -
Quality Assurance - QA/QC
Quality Engineering
Intellectt INC is seeking a CQV Engineer to support commissioning, qualification, and validation activities for pharmaceutical manufacturing systems in Massachusetts. This contract role is onsite for 6 months+ and requires close collaboration with Engineering, Quality, Manufacturing, and Validation teams to ensure systems are properly commissioned, qualified, and compliant with GMP requirements.
Responsibilities include executing CQV activities for equipment and utilities, developing and
We are seeking a motivated Onsite CQV Engineer - GMP Validation Specialist (6-Month) to join Intellectt INC in MA, United States.
Step into the Onsite CQV Engineer - GMP Validation Specialist (6-Month) role at Intellectt INC in MA, United States and grow with us.
Please review the full job details above before applying.
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).