Manufacturing Engineer I I

Aequor Technologies LLC

  • Houston, TX
  • 30+ days ago

    Highlights

    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. - Address any component or product quality issue assigned, determining root cause and completing corrective action.

    Numbers & Facts

    LocationHouston, TX
    IndustryStaffing/Employment Agencies
    Company Size100 to 499 employees

    Description


    Title: Product Engineer
    Location: Houston, TX
    Duration: 24+ Months (Possible Conversion)
    Responsibilities:

    - 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 years experience in an engineering or scientific R&D or manufacturing environment preferred.
    - Masters in engineering or scientific discipline preferred.

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