Senior Principal Quality Engineer Drug & Medical Device QMS
Listed on 2026-09-17
-
Engineering
Biomedical Engineer, Quality Engineering, Medical Device Industry
Vantive is building up capability and laboratories in Oakdale, MN, and this on-site role leads quality support for drug product and medical device R&D activities. You will work with the local R&D team to implement procedures that comply with EU MDR and the Vantive QMS, while overseeing documentation and CAPA processes.
The Senior Principal Quality Engineer requires a strong background in GLP/GMP, ISO 13485, EU GMP, and audit readiness, with a focus on regulated products and cross-functional
The following opening is for a Senior Principal Quality Engineer Drug & Medical Device QMS with Denttach LLC.
All applications are reviewed carefully by our team.
The position is based in MN, United States.
This opportunity is part of our work in IT & Technology, Engineering.
(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).