Product Engineer I
📋 Role Overview & Responsibilities
Please note candidates with a recent Masters or PhD in Biomedical Engineering have done very well in the past. Please focus your search on this type of degree.
- Work with Cataract and Vitreoretinal R&D groups on development projects resulting in achieving R&D's project goals. Tasks include supplier evaluation/qualification, component qualification, managing prototype builds, assuring assembly process is developed and documented, assure BOM's are entered and maintained correctly, assure product costs are accurate and rolled, conduct Production Readiness Review.- Support Product transfer projects either into or out of plant.- Identify and qualify alternate materials and/or components for either risk mitigation or because of obsolescence.- Maintain adequate supply of purchased components through contact with Procurement and the Suppliers. Qualify tooling and equipment as required to assure capacity.- Address any component or product quality issue assigned, determining root cause and completing corrective action.- Address any requests from other departments related to BOM's and components.- Manage product labeling.- Identify and qualify Cost Improvements.
- Communicates clearly.- Speaks/writes English.- Works well with others.- Has leadership capability and is self starter.- Ability to learn and retain many complex processes quickly.- Focuses on detail/quality.- Experience writing technical protocols/reports.- Ability to use MS Word/Excel/PowerPoint/Project.- Root cause analysis experience to determining cause of issues.- Experience in Medical Device industry - Manufacturing / Design / Quality Engineering fields- preferred.- 1-10 years experience in an engineering or scientific R&D or manufacturing environment preferred.- Masters in engineering or scientific discipline preferred.
Contract job on W2USA, Green Card, H4EAD candidate can applynot for H1B
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