Product Engineer
4 weeks ago
Date Posted: 04/08/2024
Hiring Organization: Rose International
Position Number: 461869
Job Title: Product Engineer
Job Location: Houston, TX, USA, 77054
Work Model: Onsite
Employment Type: Temporary
Estimated Duration (In months) : 24
Min Hourly Rate ($): 40.00
Max Hourly Rate ($): 46.00
Must Have Skills/Attributes: Analysis, Manufacturing, Medical device, Microsoft PowerPoint, Microsoft Project, MS Excel, MS Word
Job Description
**Only those lawfully authorized to work in the designated country associated with the position will be considered. **
**Please note that all Position start dates, and duration are estimates and may be reduced or lengthened based upon a client’s business needs and requirements. **
Notes from the Manager: 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
Description:
• 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.
• Master's in engineering or scientific discipline preferred.
Benefits:
For information and details on employment benefits offered with this position, please visit here. Should you have any questions/concerns, please contact our HR Department via our secure website.
California Pay Equity:
For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website here.
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