
Sr. R&D Engineer
- Maple Grove, MN
- $82,600 per year
- Permanent
- Full-time
- Drive complex or novel work assignments within a cross-functional team developing new single use devices and electronic medical equipment technologies and products.
- Conduct feasibility studies, develop prototypes, and perform testing and validation to optimize product designs.
- Solving engineering problems by analyzing the situation and recommending solutions or alternative actions through the design & execution of structured experimental plans.
- Understanding clinical use cases and user interface requirements to drive design decisions.
- Documenting development by writing documents, reports, memos, change requests
- May interface with Physicians to identify needs and to obtain feedback on concepts and performance of new devices and to translate customer needs into product concepts.
- Work independently to plan and schedule own activities necessary to meet timelines.
- Providing clear communication to stakeholders at key technical updates.
- Creating a strong team culture around high expectations, accountability & performance.
- May train and/or provide work direction to technicians or junior engineers.
- In all actions, demonstrating a primary commitment to patient safety and product quality by maintaining compliance with all documented quality processes and procedures.
- BS or above in Mechanical Engineering, Biomedical Engineering, or related field.
- 6+ years of engineering experience with a bachelor's degree, 4+ years with a master's degree, or 2+ years with a PhD.
- Strong technical knowledge, problem-solving abilities, collaborative mindset, and effective communication skills.
- Experience leading in an exploratory or technology development space where there are many unknowns - comfortable with grey space.
- A driven self-starter with a team-first mindset who takes accountability when working within a cross-functional team, willing and eager to leverage proven hands-on skills to design, build and test prototypes.
- Strong knowledge of design controls & risk management practices.
- Experience with injection molding, micro-molding and/or machining.
- Experience designing and validating medical device systems encompassing single use devices and electronic medical equipment
- Experience with six sigma methodologies (DOEs, capability analysis, etc)
- Familiarity with medical device standards and working with global regulatory bodies