via LinkedIn
$60K - 80K a year
Lead design transfer documentation and coordinate cross-functionally to ensure manufacturing line readiness for medical device production.
Requires 2-5 years experience in regulated manufacturing, strong manufacturing documentation skills, and knowledge of QMS and related systems.
Title: NPI Design Transfer Engineer Location: Greater Bethel Area, NH (Onsite 5 days/week) Employment Type: Contract (12 months) Status: Accepting Candidates About the role This role supports the transfer of medical device component manufacturing from development into full-scale production. You will partner closely with R&D and Manufacturing Engineering to ensure production readiness, compliance, and accurate documentation. Key Responsibilities • Lead design transfer documentation from development to production • Write and maintain work instructions, control plans, and PFMEA • Coordinate cross-functionally to confirm manufacturing line readiness • Finalize inspection procedures, sample sizes, and methods • Maintain QMS / DMR documentation through formal change control • Support post-release transfers and continuous process improvements Qualifications • Associate’s or Bachelor’s degree in Engineering or related field • 2–5 years in a regulated manufacturing environment • Strong experience with manufacturing documentation and process transfer • Working knowledge of QMS, DMR, BOMs, and job routers • Proven ability to manage timelines and cross-functional communication
This job posting was last updated on 3/4/2026