Research And Development Engineer III

Redbock - an NES Fircroft company; Maple Grove (MN); On-site; USD 90,000 - 140,000; Full time

Job summary

Redbock - an NES Fircroft company is seeking a Mechanical Engineer to advance medical device projects in Minnesota. You will design materials, processes, and equipment with minimal supervision and drive major program segments with a multidisciplinary team.

You will analyze data, develop specifications, coordinate complex tests, and document results. Responsibilities include interfacing with clinicians, updating engineering prints, and guiding technicians and junior engineers on high-impact

Qualifications

• 5-8 Years with BS, 3-6 Years with MS, 0-3 Years with PhD.

Responsibilities

• Develops new technology, products, materials, processes, or equipment with minimal supervision.
• Directs and executes plans for a major segment of complex projects.
• Interprets complex test data to establish specifications.
• Communicates results through complex reports and tests.
• Designs and coordinates engineering tests and experiments.
• Coordinates, manages, and documents project goals and progress.
• Assesses feasibility and soundness of proposed tests, products or equipment.
• Interfaces with physicians and lab personnel for feedback on concepts.
• Translates customer needs into product requirements and design specifications.
• Maintains engineering documentation and collaborates with manufacturing and regulatory teams.
• May train technicians and junior engineers; delivers high quality deliverables.
• Supports manufacturing line for hepatic artery infusion pump and accessories; updates prints; communicates with contract manufacturers.

Skills

Mechanical engineering

Design for medical devices

Engineering documentation

Problem solving

Education

Bachelor's degree in Engineering

Master's degree in Engineering

PhD in Engineering

Tools

Engineering prints

CAPA investigations

Job description

** Candidates must be W2 or C2C, no 3rd party and no candidates requiring visa sponsorship. **

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

• 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 equipmen
• 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 recommendation
• Summarizes, analyzes, and draws conclusions from complex test result
• Designs and prepares complex reports to communicate results
• Designs and coordinates complex engineering tests and experiment
• Coordinates, manages, and documents project goals and progress and recommends appropriate revision
• 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 device
• Translates customer needs into product requirements and design specification
• 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 engineer
• Demonstrates PDP/TPD system knowledge through delivery of high quality and high impact deliverable
• Primary work assignments will be involving supporting manufacturing line for hepatic artery infusion pump and accessories– updating engineering prints as necessary, communicating with the contract manufacturer and client operations/design teams, et

Qualification

• 5 - 8 Years with BS, 3 - 6 Years with MS, 0 - 3 Years with PhD
• CAPAs/NCEPs/SCAR investigations as needed, initiating and managing design changes,
• Experience with engineering prints and driving design changes in medical device is required
• Mechanical engineer Background
• Ability to take work direction and work independently.