Senior R&D Engineer — Medical Device (Onsite — Arbor Lakes, MN) Possible Temp-to-Hire

Senior R&D Engineer — Medical Device (Onsite — Arbor Lakes, MN) Possible Temp-to-Hire Osseo, United States | Posted on 02/04/2026 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 and follow us on LinkedIn: Job Description Our F500 Medical Device client has an exciting opportunity for a Senior R&D Engineer. Job Summary: Independently conducts development work as part of a major research and/or development project. Receives minimal technical direction/review on broad scope or complex projects. Viewed as an expert in one or more in-house technologies. Key Responsibilities Work with a small team of new product design engineers focused on the design of a new large bore delivery catheter. Works independently to develop key deliverables as part of a 510k regulatory submission. Deliverables include, but not limited to: CAD design, detailed print packages, specification generation and rationale, specification mapping to essential design outputs, DFMEAs, tolerance analysis, device material assessment(s), and bill of materials. Provides guidance to product and technology teams. Assesses the feasibility and soundness of alternative engineering processes, products, or equipment. Coordinates, manages, and documents project goals and progress and recommends appropriate revisions. Develop and coach others on engineering documentation. Demonstrates PDP/TPD system knowledge through coaching and delivery of high quality, high impact deliverables. Requirements Minimum of a bachelor’s degree in mechanical or biomedical engineering (or other related technical discipline). 5+ years experience in design assurance, new product development or related medical device / regulated industry experience. Experienced in design controls, print packages, tolerance analysis, GD&T. Self-motivated with a passion for solving problems and a bias for action. Strong communication skills (verbal & written). Demonstrated use of Quality tools/methodologies. Ability to effectively work and collaborate in a mixed onsite + remote environment. Demonstrated experience creating detailed technical documents. Preferred Qualifications Experience working with medical devices such as catheter or delivery systems. Quality Integration experience. ISO 13485, ISO 14971 and Quality System Regulations understanding with a focus on Design Controls and Risk Analysis. Experienced problem solver, capable of facilitating the problem-solving process. Adaptable and effective collaborator in a team environment or in self-directed work. Experience with design changes, complaint reduction, and corrective action. Other Details Schedule: 08:00:AM - 04:30:PM Work Setup: Onsite — Arbor Lakes, MN 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. #J-18808-Ljbffr Pharmavise Corporation