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Director Engineering Medical Device Jobs in Minnesota

DivIHN

Senior Systems Engineer (Medical Device)

Plymouth, MN · On-site

$109K - $149K/yr

Senior Systems Engineer (Medical Device) Duration: 12 Months Location: Plymouth, MN Only W2 ... Perform the activities associated with the systems engineering of one or more products in various ...

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$71.5K

$190.7K

$248.8K

How much do director engineering medical device jobs pay per year?

As of Sep 1, 2026, the average yearly pay for director engineering medical device in Minnesota is $190,701.00, according to ZipRecruiter salary data. Most workers in this role earn between $138,600.00 and $247,800.00 per year, depending on experience, location, and employer.

What is a director engineering medical device?

A Director of Engineering in the medical device industry leads the design, development, and testing of medical technologies while ensuring compliance with regulatory standards. They manage engineering teams, oversee project timelines, and collaborate with cross-functional departments, including R&D, quality assurance, and manufacturing. Their role involves strategic planning, resource allocation, and risk management to drive innovation and bring safe, effective medical devices to market.

What are the key skills and qualifications needed to thrive in the director engineering medical device position?

To excel as a Director Engineering Medical Device, you need extensive experience in engineering management, regulatory compliance (such as FDA and ISO standards), and a background in medical device design or related technical fields. Proficiency with product lifecycle management (PLM) tools, design control systems, and quality management certifications like Six Sigma or PMP are highly valuable. Outstanding leadership, strategic thinking, and the ability to communicate effectively across multidisciplinary teams help set top performers apart. These capabilities are crucial to successfully guide high-stakes projects, ensure regulatory compliance, and drive innovation in a highly regulated industry.

What are the typical challenges faced by a director of engineering in the medical device industry?

A Director of Engineering in the medical device field often navigates complex regulatory requirements while balancing innovation and speed-to-market. They frequently manage cross-functional teams, oversee rigorous testing and verification processes, and must ensure that all products meet strict quality and safety standards. Collaboration with regulatory, clinical, and marketing teams is essential to align technical development with business objectives. Additionally, adapting to evolving technology and changes in regulatory landscapes can present ongoing challenges, making strong leadership and adaptability key assets.

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What job categories do people searching Director Engineering Medical Device jobs in Minnesota look for?

The top searched job categories for Director Engineering Medical Device jobs in Minnesota are:

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Cities in Minnesota with the most Director Engineering Medical Device job openings:

Director Engineering Medical Device jobs near you
Infographic showing various Director Engineering Medical Device job openings in Minnesota as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 17% Part Time, and 5% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $190,701 per year, or $91.7 per hour.

Senior Systems Engineer (Medical Device)

Plymouth, MN • On-site

DivIHN
See more jobs at DivIHNexternal

$109K - $149K/yr

Contractor

Posted 4 days ago

Job description

For further inquiries regarding the following opportunity, please contact one of our Talent Specialists, Sri Balan at (217)-279-2447 or Hema (630)-847-0275
Title: Senior Systems Engineer (Medical Device)
Duration: 12 Months
Location: Plymouth, MN
Only W2 candidates are eligible for this position. Third-party or C2C candidates will not be considered.
Description:
Your Role:
  • Our PrisMax systems are used in the intensive care unit (ICU) to support patients experiencing life-threatening acute kidney injury. Clinicians rely on our devices to deliver continuous renal replacement therapy (CRRT), helping to maintain critical kidney function while patients recover. We're building new platforms, devices, and connected systems to make therapy administration more efficient, consistent, and intuitive-so care teams can focus on the patient.
  • Client is seeking a System Engineer (contract) to support the overall technical direction of Acute Therapies products. Based on your technical skills, you will drive various portions of the product development cycle at stages ranging from feasibility through lifecycle management. Tasks may include development of design concepts/changes, product requirements management, traceability, DHF structure & maintenance, product risk management, system integration, verification, and validation of medical devices.

What you'll be doing:
  • Perform the activities associated with the systems engineering of one or more products in various stages of the product lifecycle from new product development to post-market surveillance
  • Understand clinical and user needs and apply them to product realization
  • Capture inputs for requirements from various sources such as user needs, regulatory standards, human factors, quality, manufacturing, service, etc.
  • Use knowledge of technology, process, and/or therapy domains to drive solutions and product design realization from a systems perspective
  • Craft design concepts and research methodologies that best meet current and future customer / business needs for a product or process domain area
  • Create and maintain design history file elements
  • Facilitate an improved understanding of the interrelationship between requirements, risk and reliability
  • Anticipate technical challenges and risk scenarios and prepare, lead, and execute mitigation strategies to ensure optimal results
  • Resolve systems-related technical issues by applying problem-solving tools such as cause-and-effect diagrams, Pareto charts, etc.
  • Propose and drive solutions to technical problems that are ambiguous and diverse in scope
  • Perform impact assessments on the requirements on an ongoing basis for any proposed design / material / process changes or observations from field / service / manufacturing. As needed, propose recommended mitigations with rationale.
  • Influence stakeholders and cross-functional team members within the project
  • Drive adherence to FDA, ISO and IEC design control procedures, regulations and standards
  • Use various software tools and programs to complete the above responsibilities

What you'll bring:
  • Bachelor's degree or Master's degree and three years or more of relevant experience, with a degree in Electrical, Software, Mechanical, Biomedical, or a related engineering or science discipline
  • Prior experience in medical devices, preferably for intensive care unit (ICU) or kidney care domains
  • Sound knowledge of systems engineering and related areas such as electro-mechanical and software engineering
  • A track record in electro-mechanical system development, preferably in medical devices or other regulated products such as aerospace, automobile, or military
  • Prior experience with internet-connected, software-enabled devices and/or cyber security
  • Working knowledge of system modeling language (SysML or UML) and requirement management tools
  • Knowledge of DOORS and Jama requirements management tools preferred
  • Knowledge of Teamcenter, TrackWise8, JIRA, and ALM preferred
  • Familiar with statistical methods/tools for design and verification, e.g. DOE, sample size
  • Success in working with multi-functional, global teams
  • Excellent interpersonal, communication, and influencing skills
  • Ability to work independently
  • Ability to manage simultaneously several projects and shift priority according to needs
  • Demonstrated strong analytical and problem-solving skills
  • Ability to solve problems, develop solutions, and make recommendations in collaboration with project leaders
  • Creative Problem Solver - identify technical risks up front, develop and execute mitigations and provide team direction on how to remove or avoid roadblocks
  • Ability to deliver results according to the plan

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