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- 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.
- 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 year of experience in an engineering or scientific R&D or manufacturing environment preferred.
- Targeting a Masters in Biomedical Engineering.
Product Engineer I - Houston, United States - Astrix Inc
Description
Exciting 2 year contract Product Engineer opportunity to work for a global leader dedicated to helping people see brilliantly. The largest device company in the world – with complementary businesses in Surgical and Vision Care.New Grads with an Advanced degree in Biomedical Engineering with High a GPA
Medical, Dental, Holiday, PTO and 401 K
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.
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