Quality Engineer — Med Device; FDA/ISO/GMP
Listed on 2026-10-07
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Quality Assurance - QA/QC
Quality Engineering -
Engineering
Quality Engineering, Process Engineer, Biomedical Engineer
Tecomet, Inc. is seeking a Quality Engineer I to help ensure adherence to quality systems and customer requirements. The role focuses on continuous improvement within a medical device manufacturing context, aligning with GMP/GDP practices and regulatory standards.
You will support MRB/ RMA processes, prepare FMEA/PPAP documents, and assist in process validations while working with cross-functional teams to resolve quality, cost, and schedule issues.
Our organisation is growing, and we are hiring a Quality Engineer I — Med Device (FDA/ISO/GMP) in Warsaw, IN, United States.
Join Tecomet, Inc and contribute to our ongoing work.
Take a moment to read everything above and see whether this role is right for you.
This posting is for the Quality Engineer I — Med Device (FDA/ISO/GMP) role at Tecomet, Inc, based in Warsaw, IN, United States.
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