Product Engineer

3 weeks ago


Houston, United States Rose International Full time

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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