Remote Validation Engineer – GMP, CSV & CQV Focus
-
Quality Assurance - QA/QC
-
Engineering
Job Description & How to Apply Below
Syner-G is seeking a Validation Engineer to support CQV and CSV activities across equipment, utilities, facilities, laboratory systems, and manufacturing processes. You will develop, execute, review, and maintain validation lifecycle documentation with a focus on Kneat-based workflows.
The role requires 4–7 years in biotech/pharma/medical devices, strong FDA cGMP knowledge, and hands-on validation experience. Collaboration with Engineering, QA, and Regulatory teams is essential.
We would love to welcome a new Remote Validation Engineer – GMP, CSV & CQV Focus to our group in Plainville, MA, United States.
This posting is for the Remote Validation Engineer – GMP, CSV & CQV Focus role at Bio Space, based in Plainville, MA, United States.
We are looking to fill the Remote Validation Engineer – GMP, CSV & CQV Focus position at Bio Space in Plainville, MA, United States.
(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).
View / Apply for Jobs
Matching My Jurisdiction