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Director Medical Device Product Development Jobs in Michigan

Medical Device Assembly

Wixom, MI · On-site

$16 - $17/hr

Excel Medical Products in Wixom, MI is looking for a detail-oriented Medical Device Assembler to join their growing team. This is a great opportunity to be part of a precision-driven environment ...

Medical Device Assembly

Wixom, MI · On-site

$16 - $17/hr

Excel Medical Products in Wixom, MI is looking for a detail-oriented Medical Device Assembler to join their growing team. This is a great opportunity to be part of a precision-driven environment ...

Medical Device Assembly

Wixom, MI · On-site

$16 - $17/hr

Excel Medical Products in Wixom, MI is looking for a detail-oriented Medical Device Assembler to join their growing team. This is a great opportunity to be part of a precision-driven environment ...

Develop a strong understanding of Medical Device market dynamics, including regulatory and ... Monitor competing products and the competitive landscape to inform strategy and positioning.

Conduct the development and evaluation of medical device designs which meet defined product requirements and that are optimized for safe clinical solutions, production, reliability, and overall cost ...

Medical Device Product Development * Lead projects and evaluate design changes related to existing products to maintain business continuity. * Develop and evaluate medical device designs which meet ...

Medical Device Product Development * Lead projects and evaluate design changes related to existing products to maintain business continuity. * Develop and evaluate medical device designs which meet ...

Conduct the development and evaluation of medical device designs which meet defined product requirements and that are optimized for safe clinical solutions, production, reliability, and overall cost ...

... and medical device products while driving process robustness, manufacturing readiness, and ... The Role Reporting to the Director, Pharmaceutical Technologies , the Manager, Process Development ...

... and medical device products while driving process robustness, manufacturing readiness, and ... The RoleReporting to the Director, Pharmaceutical Technologies, the Manager, Process Development ...

Manager, Process Development

Brighton, MI · On-site

$100K - $120K/yr

... and medical device products while driving process robustness, manufacturing readiness, and ... The Role Reporting to the Director, Pharmaceutical Technologies , the Manager, Process Development ...

Senior Portfolio Manager

Kalamazoo, MI · On-site

$85 - $125/hr

Bachelors degree required * 6+ years of work experience required * MBA preferred * 3+ years of medical device experience preferred * New product development or marketing experience preferred

Medical Assembler

Dexter, MI · On-site

$18.50 - $20/hr

Assemble components such as modules, circuit boards, panels, frames, cables, drawers, and other medical device products. * Follow visual aids, process layouts, diagrams, schematics, process flow ...

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Showing results 1-20

Director Medical Device Product Development information

What is the difference between Director Medical Device Product Development vs Product Manager Medical Devices?

AspectDirector Medical Device Product DevelopmentProduct Manager Medical Devices
ResponsibilitiesOversees entire product development lifecycle, manages teams, sets strategic directionFocuses on product planning, feature definition, and market analysis
Required CredentialsEngineering or life sciences degree, experience in medical device development, regulatory knowledgeBackground in engineering, marketing, or life sciences, familiarity with medical device regulations
Work EnvironmentLeadership role in R&D or product development departments, cross-functional teamsCollaborates with engineering, marketing, and sales teams, often in a more tactical role

The main difference is that the Director Medical Device Product Development leads and manages the entire development process and teams, focusing on strategic oversight, while the Product Manager Medical Devices concentrates on product planning and market needs. The director role involves higher-level management and regulatory oversight, whereas the product manager handles day-to-day product features and customer requirements.

What are the most commonly searched types of Medical Device Product Development jobs in Michigan?

The most popular types of Medical Device Product Development jobs in Michigan are:

What are popular job titles related to Director Medical Device Product Development jobs in Michigan?

For Director Medical Device Product Development jobs in Michigan, the most frequently searched job titles are:

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Cities in Michigan with the most Director Medical Device Product Development job openings:

Director, New Product Development

Caledonia, MI

Full-time

Re-posted 14 days ago


Job description

Summary

The Director, New Product Development, is responsible for driving the ideation, development, and commercialization of innovative medical device products across Aspen Surgical’s portfolio. Reporting to the VP, Marketing & Product Development, this leader will be tasked with expanding the engineering team and building out and executing against a robust new product pipeline to deliver organic revenue growth. The Director will have the autonomy to build and organize the function as the business grows, and will partner closely with Marketing, Regulatory, Quality, and Operations to deliver differentiated products that meet rigorous clinical, regulatory, and market requirements. This is a change-oriented role requiring an established leader who can create structure from ambiguity, drive pace in a fast-moving environment, and build the cross-functional credibility needed to move critical company priorities forward.

In This Position, You Will Have the Opportunity To

  • Define and execute the new product development roadmap in alignment with the commercial strategy set by the VP, Marketing & Product Development.
  • Partner with Marketing and Sales to identify unmet clinical needs and prioritize the development pipeline.
  • Lead project pipeline reviews, stage-gate processes and portfolio reviews with senior and executive leadership.
  • Develop and lead an expanded NPD team, currently comprising one manager and four engineers.
  • Assess team structure and capabilities; design and build the organization as the portfolio and pipeline expand.
  • Foster a culture of innovation, accountability, and continuous improvement across the team.
  • Manage resource allocation and capacity planning across concurrent development programs.
  • Oversee all phases of design and development — from concept through commercialization — in compliance with design control requirements.
  • Ensure on-time, on-budget delivery of product launches with appropriate clinical and technical validation.
  • Lead risk management activities including design FMEAs, usability studies, and human factors engineering.
  • Collaborate with Regulatory Affairs to define submission strategies (510(k), De Novo, etc.) and support technical documentation.
  • Champion compliance with FDA 21 CFR Part 820, ISO 13485, and applicable international standards.
  • Partner with Operations to ensure robust design transfer processes and manufacturing scalability.
  • Identify and manage external development partners, contract design firms, and technology licensors.
  • Engage key opinion leaders and surgeon advisory boards for clinical input and product validation.
  • Stay current with emerging technologies, best practices, and industry trends, including the application of AI to accelerate development processes and improve design quality.

What You Need to Succeed in This Position

Required

  • Bachelor’s degree in Engineering, Biomedical Sciences, or related field.
  • 10+ years of medical device product development experience, including 5+ years in a team leadership role.
  • Proven track record of FDA-cleared or approved product launches.
  • Deep knowledge of design controls, 21 CFR Part 820, and ISO 13485.
  • Strong project management and stage-gate methodology experience.
  • Experience with international product approval processes and required documentation.

 

Preferred

  • Advanced degree (e.g. MS, MBA) with PMP or equivalent project management certification.
  • Experience with OR workflow and sterile/single-use product environments.
  • Familiarity with SPD processes and the corresponding products required for sterile processing.
  • Familiarity with endoscope reprocessing, and the standards and guidelines governing the process.
  • M&A integration or technology acquisition experience.

 

Leadership Competencies

  • Strategic vision and business acumen.
  • Inspirational team leadership and talent development.
  • Executive presence and communication.
  • Decision-making under ambiguity.
  • Cross-functional influence without authority.
  • Organizational design and change management.
  • Customer and clinical focus.
  • Innovation mindset and intellectual curiosity.Â