Process Engineer III — Medical Device (Onsite — Maple Grove, MN) Contract

Pharmavise CorporationMaple Grove, MN
21dOnsite

About The Position

Our F500 Medical Device client has an exciting opportunity for a Process Engineer III. Job Summary: Develops new technology, products, materials, processes, or equipment with minimal supervision. Independently, or as a member of a team, develops, directs, and executes plans for a major segment of complex projects. Compiles and analyzes operational, test, and research data to establish technical specifications for designing or modifying products, processes, and materials.

Requirements

  • 3 - 5 Years with BS
  • Able to collaborate effectively with cross functional peers
  • Prior experience in a regulated industry
  • Prior experience with manufacturing and/or process development

Responsibilities

  • Consistently generates innovative and unique solutions to market needs and submits idea disclosures.
  • Work is expected to result in the development of new or refined products, processes or equipment.
  • Successfully completes complex engineering work in one or more of the following: technology development, product design and development, test of materials or products, preparation of specifications, process study, research investigation (animal and clinical studies), and report preparation.
  • Selects techniques to solve complex problems and make sound design recommendations.
  • Summarizes, analyzes, and draws conclusions from complex test results.
  • Designs and prepares complex reports to communicate results to technical community.
  • Designs and coordinates complex engineering tests and experiments.
  • Coordinates, manages, and documents project goals and progress and recommends appropriate revisions.
  • Assesses the feasibility and soundness of proposed engineering evaluation tests, products or equipment.
  • Interfaces with Physicians/Cath Lab personnel to obtain feedback on concepts and performance of new devices.
  • Translates customer needs into product requirements and design specifications.
  • Responsible for engineering documentation
  • Works cooperatively with process development, quality, manufacturing, regulatory, clinical, and marketing on complex projects to ensure project success.
  • May train and/or provide work direction to technicians and entry-level engineers.
  • Demonstrates PDP/TPD system knowledge through delivery of high quality and high impact deliverables.
  • Build Quality into all aspects of their work by maintaining compliance to all quality requirements.
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