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

Pharmavise Corporation; Maple Grove (MN); On-site; USD 90,000 - 120,000; Full time

Job summary

Pharmavise Corporation is seeking a Process Engineer III for an onsite Maple Grove, MN contract position. The role focuses on translating customer needs into device requirements, coordinating complex tests, and interfacing with clinicians to refine concepts.

The candidate will work across engineering, quality, regulatory, manufacturing, and marketing to deliver high-impact results, with 3–5 years of relevant experience and a BS in engineering. This is a 12-month assignment based in Maple Grove.

Qualifications

• 3 - 5 years of experience with a BS in engineering or related field.
• Able to collaborate effectively with cross-functional peers.
• Prior experience in a regulated industry.
• Prior experience with manufacturing and/or process development.

Responsibilities

• Generate innovative solutions for market needs and document idea disclosures.
• Complete complex engineering tasks across technology development, product design, testing, specifications, and report preparation.
• Select techniques to solve complex problems and provide sound design recommendations.
• Analyze complex test results and communicate findings to the technical community.
• Design and coordinate complex tests and experiments; prepare complex reports.
• Coordinate, manage and document project goals and progress; propose revisions as needed.
• Assess feasibility and soundness of proposed tests, products or equipment.
• Interface with physicians and clinical staff to gather feedback on concepts and performance of new devices.
• Translate customer needs into product requirements and design specifications.
• Maintain engineering documentation and collaborate with process development, quality, manufacturing, regulatory, clinical, and marketing teams.

Skills

Cross-functional collaboration

Regulated industry experience

Manufacturing/process development

Education

BS in Engineering

Job description

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

Maple Grove, United States | Posted on 12/04/2025

From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to complex compliance issues. We collaborate with our partners by providing technical expertise in Quality, Regulatory Compliance and Manufacturing Science and Technology. Our business mission is to ensure our clients exceed their compliance goals while improving patient health and safety. Visit us at www.pharmavise.com and follow us on LinkedIn: https://www.linkedin.com/company/pharmavisecorp

Job Description

OurF500 Medical Deviceclient has an exciting opportunity for a Process Engineer III.

Key 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.

Quality Systems Duties and Responsibilities

Build Quality into all aspects of their work by maintaining compliance to all quality requirements.

Qualifications

• 3 - 5 Years with BS

Additional Job Specific Requirements

• 1. Able to collaborate effectively with cross functional peers
• 2. Prior experience in a regulated industry
• 3. Prior experience with manufacturing and/or process development

Other Details

• Schedule: 08:00:AM - 04:30:PM
• Work Setup: Onsite 5 days per week in Maple Grove, MN
• Contract Duration: 12 Months (1/5/2026 - 1/4/2027)

Pharmavise Corporation is an Equal Opportunity Employer and does not discriminate on the basis of race or ethnicity, religion, sex, national origin, age, veteran disability or genetic information or any other reason prohibited by law in employment.