Senior R&D Engineer

Posted Yesterday
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New Brighton, MN, USA
In-Office
94K-131K Annually
Senior level
Healthtech
The Role
Leads medical device research and development from concept through design transfer. Owns technical scope, product specifications, prototyping, verification and validation planning, risk documentation, engineering deliverables, supplier capability evaluation, regulatory compliance, and manufacturing transfer. Collaborates with marketing, clinical, regulatory, supply chain, and manufacturing teams while developing prototypes, evaluating emerging technologies, troubleshooting design issues, and communicating project progress to stakeholders and senior leadership.
Summary Generated by Built In

At Tactile Medical, we specialize in developing at-home therapy devices to treat lymphedema, chronic venous insufficiency and respiratory illnesses.

The Sr Research and Development Engineer is responsible for leading technology and product development efforts as a core member of the Product Development team and executing necessary engineering deliverables to ensure the Product Development goals and objectives are met. They influence decision-making at all levels of the product development life cycle and will maintain technical ownership of design-related project deliverables from concept through design transfer. This person actively collaborates with functions throughout Tactile Medical and leverages cross-functional partnerships to drive product and technology roadmap development.

• As a product SME and technical leader, drive project objectives with minimal oversight ensuring project milestone progression is clearly communicated and understood by cross-functional partners.
• Create and test prototypes for design concepts that may apply to projects 1-5 years out. This includes mechanical and electrical components prototyping using additive manufacturing techniques and other quick-turn methods. Preferably able to execute low level programming to incorporate electrical system functionality into prototypes.
• Identify, investigate, and test feasibility of new technologies for application to future projects.
• Execute the technology development roadmap which is tied to the long-term goals of Tactile Medical
• Lead cross-functional efforts with marketing, clinical, and regulatory to drive next-steps of concepts
• Manage the overall technical scope of a product development effort including translating product requirements into product specifications, product design, verification and validation plans, product cost and technical schedule
• Ensure all engineering deliverables outlined in the Design and Development Procedure are accurate and completed on time
• Drive completion of design input requirements through partnership with cross-functional stakeholders
• Ownership of engineering efforts to translate design input requirements into product specifications
• Throughout the product development lifecycle, ensure the needs of supply chain are met when determining existing and new supplier’s capabilities
• Manage and/or execute R&D engineering deliverables to maintain overall project schedule, with an emphasis on technical tasks and deliverables
• Contribute to creation of risk management documentation related to design risks and hazards
• Develop and maintain engineering documentation (drawings, specifications, bills of materials, etc.) and ensure quality, completeness, accuracy, and timeliness to support project requirements
• Ensure product design complies with relevant regulatory/IEC standards
• Prepare and present product development presentations for senior management
• Support manufacturing’s performance in meeting quality, productivity, and delivery objectives
• Communicate events and project updates effectively to core team members in written and verbal formats
• Troubleshoot new and existing products/process problems as related to design, material, or processes
• Ensure process and procedures adhere to internal and external requirements
• Participate in Design Transfer to Manufacturing
• Other duties as assigned

Education & Experience
Required:
• Bachelor's Degree in Mechanical Engineering, Electrical Engineering or similar field required
• 6+ years of engineering experience, preferably within medical device products
• OR Master’s Degree in Engineering or similar field with 4+ years of engineering experience, preferably within medical device products

Preferred:
• Experience in leading medical device technical development efforts, through all phases of product development
• Experience utilizing a stage / phase gate process within the medical device industry
• Experience using SolidWorks, AutoCAD, or other CAD modeling software
• Experience in digital signal processing

Knowledge & Skills
• Influence without authority, develop strong relationships cross-functionally and collaborate through conflict to accomplish project goals under tight deadlines
• Strong prioritization and reprioritization skills
• Demonstrated problem solving skills and analytical abilities
• Easily adapts to changing business needs and adept at juggling numerous projects and deadlines
• High proficiency in Microsoft Word, PowerPoint, and Excel
• Results-oriented and naturally focuses efforts on innovative and cost-effective solutions
• Excellent written/verbal communication and presentation skills to clearly articulate concepts, status, and challenges to a broad range of audiences
• Operate as a strong team player with a high degree of flexibility
• Facilitate meetings of varying sizes, balancing the needs, voices, and concerns of all participants
• Electrical, mechanical prototyping
• Ability to interpret electrical and mechanical schematics
• Basic understanding of lean principles and processes
• Curious and questioning mindset which can be applied in new development as well as towards continuous improvement
• Draw from diverse experiences applying engineering knowledge to different situations
• Ability to collaborate with both technical and non-technical team members

Competencies
• Action Orientated
• Directing Others
• Influencing
• Flexible
• Functional/Technical Skills
• Teamwork
• Communication
• Process oriented
• Priority Setting
• Problem Solving
• Innovative

Our total compensation package includes medical, dental and vision benefits, retirement benefits, employee stock purchase plan, paid time off, parental leave, family medical leave, volunteer time off and additional leave programs, life insurance, disability coverage, and other life and work wellness benefits and discounts. Benefits may be subject to generally applicable eligibility, waiting period, contributions, and other requirements and conditions.


Below is the starting salary or hourly range for this position, although offers may differ based on the candidate's location, job-specific knowledge, skills and experience.

US Pay Range
$93,600$131,040 USD

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Skills Required

  • Bachelor's degree in Mechanical Engineering, Electrical Engineering, or a similar field
  • 6+ years of engineering experience, preferably with medical device products
  • Alternatively, a Master's degree in Engineering or a similar field with 4+ years of engineering experience, preferably with medical device products
  • Experience leading medical device technical development efforts through all phases of product development
  • Experience using a stage or phase-gate process within the medical device industry
  • Experience with SolidWorks, AutoCAD, or other CAD modeling software
  • Experience in digital signal processing
  • Electrical and mechanical prototyping skills
  • Ability to interpret electrical and mechanical schematics
  • Basic understanding of lean principles and processes
  • Proficiency in Microsoft Word, PowerPoint, and Excel
  • Strong written, verbal communication, presentation, problem-solving, prioritization, and cross-functional collaboration skills
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The Company
HQ: Minneapolis, MN
1,048 Employees
Year Founded: 1995

What We Do

Tactile Medical is one of the fastest growing companies in medical devices. As a leader in treatment options for lymphedema and venous ulcer therapies, Tactile Medical develops advanced home therapy devices to improve health and quality of life for patients with chronic swelling . Headquartered in Minneapolis, Minnesota, we advocate for patient access and serve tens of thousands of patients through a direct national network of product specialists and trainers, reimbursement experts, patient advocates, and clinical staff.

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