Process Engineer III

Technical Recruiter for Engineering Division;
Life Sciences, Med Device, Pharma, Aerospace and Manufacturing Working direct hire roles and contract…

Location: Maple Grove, MN

Work Arrangement: Onsite, 5 days/week

The R&D Engineer III is responsible for developing new technologies, products, materials, processes, and equipment with minimal supervision. This role independently—or as part of a team—plans, directs, and executes major segments of complex engineering projects. The engineer will compile and analyze operational, test, and research data to establish technical specifications for designing or modifying products, processes, and materials.

• Generate innovative and unique solutions to market needs; submit idea disclosures.
• Develop new or refined products, processes, and equipment.
• Complete complex engineering work in areas such as:
• Technology development
• Product design and development
• Material and product testing
• Specification preparation
• Process studies
• Research investigations (including animal and clinical studies)
• Technical report preparation

• Select appropriate techniques to solve complex engineering problems.
• Analyze and summarize complex test results; draw meaningful conclusions.
• Prepare detailed technical reports for internal and external stakeholders.
• Design and coordinate complex engineering tests and experiments.
• Assess feasibility and soundness of proposed tests, products, or equipment.

• Interface with physicians and cath lab personnel to gather feedback on device concepts and performance.
• Translate customer needs into product requirements and design specifications.
• Collaborate with process development, quality, manufacturing, regulatory, clinical, and marketing teams to ensure project success.
• Provide training or work direction to technicians and entry-level engineers as needed.
• Coordinate and document project goals, progress, and recommended revisions.
• Maintain responsibility for engineering documentation.
• Demonstrate strong PDP/TPD system knowledge through high-quality deliverables.

• Build quality into all aspects of work by maintaining compliance with all applicable quality system requirements.

• 3–5 years of relevant engineering experience.

• Strong ability to collaborate with cross-functional peers.
• Experience working in a regulated industry (medical device preferred).
• Prior experience in manufacturing and/or process development.
• Must be onsite 5 days per week.

• Mid-Senior level

• Contract

• Industries
• Medical Equipment Manufacturing

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