GMP Manufacturing Engineer — Medical Devices & Validation
Listed on 2026-10-16
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Engineering
Validation Engineer, Quality Engineering, Manufacturing Engineer
TAE Life Sciences in Southern California is hiring a Manufacturing Engineer to build and scale production capabilities in a GMP environment. You will collaborate with scientists, design engineers, and quality teams to drive scalable manufacturing and ensure compliant processes.
Requirements include a Bachelor’s in a related field and 5+ years in thin film processing (CVD/PVD/thermal evaporation). Core hours are 8am-5pm, with a hybrid role based in Irvine, CA.
The GMP Manufacturing Engineer — Medical Devices & Validation position in the Engineering field is open for applications.
Full responsibilities and requirements are described in the listing above.
Learn more about the GMP Manufacturing Engineer — Medical Devices & Validation role in the description above.
We appreciate your interest in this position.
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