Medical Device Process Engineer II — Regulatory Focus
Listed on 2026-10-07
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Engineering
Manufacturing Engineer, Process Engineer, Quality Engineering, Biomedical Engineer
Planet Pharma in Minnesota seeks a Manufacturing Process Engineer to design and optimize production layouts for cardiovascular combination products. You will support testing methods, tooling, and yield improvements while ensuring compliance with regulatory requirements.
Responsibilities include reducing scrap, dispositioning nonconforming product, maintaining SPC-driven processes, and guiding design and production procedures.
The Medical Device Process Engineer II — Regulatory Focus role at Planet Pharma is now open for applications in Plymouth, MN, United States.
The position is based in Plymouth, MN, United States.
This opportunity is part of our work in Engineering.
The advertised compensation is 70..
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Medical Device Process Engineer II — Regulatory Focus role in the description above.
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