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Medical Device Product Development Manager Jobs (NOW HIRING)

Abbott

Development Quality Engineer II

Plymouth, MN · On-site

$35 - $38/hr

Seeking a Quality Engineer with experience in medical device product development to support risk management, design controls, verification and validation, and regulatory compliance for electro ...

iRESTORE

Product Development Manager

Los Angeles, CA · On-site

$80 - $110/hr

Required Qualifications * 3-5 years of experience in product development, product management, or project management within medical devices and/or consumer products, including beauty, wellness, or ...

Legrand

Product Development Manager

Warsaw, IN · On-site

$110 - $140/hr

The Product Development Manager is a key leader in bringing innovative products to market. This ... LNCA offers comprehensive medical, dental, and vision coverage * high employer 401K match * paid ...

UFP Industries

Product Development Manager

Blanchester, OH · On-site

$101K - $127K/yr

Job Summary We are seeking an experienced and highly motivated Senior Industrial Designer / Product Development Manage with 5-7 years of experience leading product development and innovation ...

Nood

Technical Product Development Manager

New York, NY · Remote

$85K - $110K/yr

Manage device development critical paths from industrial design through tooling, engineering ... medical devices, biotech, or consumer goods manufacturing * Experience owning launch timelines ...

Nood

Technical Product Development Manager

New York, NY · Hybrid

$85K - $110K/yr

Manage device development critical paths from industrial design through tooling, engineering ... medical devices, biotech, or consumer goods manufacturing * Experience owning launch timelines ...

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Medical Device Product Development Manager information

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$127K

$144.5K

How much do medical device product development manager jobs pay per year?

As of Sep 5, 2026, the average yearly pay for medical device product development manager in the United States is $126,987.00, according to ZipRecruiter salary data. Most workers in this role earn between $114,500.00 and $143,000.00 per year, depending on experience, location, and employer.

What does a medical device product development manager do?

A Medical Device Product Development Manager oversees the entire process of bringing a medical device from the concept stage to market launch. They coordinate cross-functional teams, manage timelines, ensure compliance with regulatory standards, and oversee testing and validation of products. Their responsibilities also include working with engineers, designers, and regulatory specialists to ensure the device meets safety, efficacy, and user needs. Ultimately, they play a critical role in ensuring that new medical devices are developed efficiently, safely, and in compliance with industry standards.

How does a medical device product development manager typically collaborate with cross-functional teams during the development process?

A Medical Device Product Development Manager works closely with cross-functional teams, including engineering, regulatory affairs, quality assurance, marketing, and clinical experts, to ensure that product requirements are met throughout each development phase. They facilitate regular meetings to align on project milestones, address potential risks, and incorporate feedback from various stakeholders. This collaborative environment helps ensure that the final product complies with regulatory standards and meets market needs, making strong communication and project management skills essential in this role.

What are the key skills and qualifications needed to thrive as a medical device product development manager, and why are they important?

To thrive as a Medical Device Product Development Manager, you need expertise in engineering or life sciences, experience with product lifecycle management, and knowledge of regulatory requirements, often supported by a relevant degree. Familiarity with CAD software, project management tools, and compliance systems such as ISO 13485 or FDA regulations is typically required. Strong leadership, cross-functional communication, and problem-solving skills help drive innovation and align diverse teams. These competencies are vital to ensure products are developed efficiently, safely, and in compliance with industry standards.

What is the difference between Medical Device Product Development Manager vs Medical Device Quality Assurance Specialist?

AspectMedical Device Product Development ManagerMedical Device Quality Assurance Specialist
CredentialsEngineering degree, certifications like PMP or PDMAQuality assurance certifications like CQE, ISO auditor
Work EnvironmentDesign teams, R&D, cross-functional project groupsQuality labs, compliance departments, manufacturing oversight
Industry UsageLeading product development from concept to launchEnsuring products meet quality and regulatory standards

The Medical Device Product Development Manager focuses on designing and developing new medical devices, managing cross-functional teams, and bringing products to market. In contrast, the Medical Device Quality Assurance Specialist ensures that products meet quality standards and regulatory requirements throughout the development and manufacturing process. Both roles are essential in the medical device industry but serve different functions in product lifecycle management.

What is medical device product development?

Medical device product development involves designing, testing, and bringing new medical devices to market, ensuring they meet safety and regulatory standards. A Medical Device Product Development Manager oversees this process, coordinating cross-functional teams, managing timelines, and ensuring compliance with industry regulations such as FDA or ISO standards.

What cities are hiring for Medical Device Product Development Manager jobs?

Cities with the most Medical Device Product Development Manager job openings:

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

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

What states have the most Medical Device Product Development Manager jobs?

States with the most job openings for Medical Device Product Development Manager jobs include:

Medical Device Product Development Manager jobs near you
Infographic showing various Medical Device Product Development Manager job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $126,987 per year, or $61.1 per hour.

Product Development Compliance Engineer

SharkNinja

Needham, MA • On-site

Full-time

Re-posted 28 days ago

SharkNinja rating

8.2

Company rating: 8.2 out of 10

Based on 5 frontline employees who took The Breakroom Quiz

47th of 161 rated electronics manufacturers

Job description

Product Safety & Compliance Engineer

NPD Compliance - Household Appliances & Medical Devices

The Product Safety & Compliance Engineer partners with global product development teams and external certification bodies (NRTLs and agency labs) to drive product safety compliance and certification from concept through mass production. The portfolio is primarily household appliances, with medical and wellness devices. This is a hands-on engineering role: you will influence product design early, own the certification path, and be the voice of compliance in the room - including when that means pushing back.

What You'll Do
  • Own certification and risk-analysis activities for multiple new product development projects simultaneously, from product concept through mass production.
  • Translate complicated regulatory and standards requirements into simple, actionable design guidance for design engineers and product managers - early enough to shape the design, not just audit it after the fact.
  • Review product designs and constructions against applicable safety standards; identify compliance gaps and propose practical, engineering-grounded mitigation.
  • Define certification deliverables, sample plans, and timelines with development teams and third-party labs; drive agency evaluations to close on schedule.
  • Execute risk analysis (hazard analysis, DFMEA) and maintain traceable compliance documentation across the product lifecycle.
  • Present project status, certification timelines, and risks in weekly cross-functional reviews - clearly, confidently, and without burying the bad news.
  • Assess design changes (ECNs) for certification impact and manage agency follow-up activities through launch and post-launch.
  • Contribute to continuous improvement of compliance processes, templates, and stage-gate deliverables.
Required Qualifications
  • Bachelor's degree in Engineering (Electrical, Mechanical, Biomedical, or a related engineering discipline). An engineering degree is a firm requirement for this role.
  • Hands-on experience with both product design and the certification process: you have taken electromechanical products through agency evaluation (NRTL, CB Scheme, or equivalent) from concept to production, and you have worked on the design side - not solely in documentation, auditing, or quality-records roles.
  • 2-4 years of relevant experience with consumer, commercial, or medical/wellness electromechanical products.
  • Working knowledge of general product safety standards: UL and IEC standards for household appliances (e.g., the IEC/UL 60335 series) and for medical and wellness devices (e.g., the IEC 60601 family).
Preferred
  • Direct experience interfacing with NRTLs, agency labs, or Notified Bodies.
  • Familiarity with EMC and multi-market certification schemes (e.g., cULus, CE, UKCA, CB).
  • Exposure to FDA-regulated medical or wellness devices.
Who You Are
  • A clear communicator: you make complex regulatory requirements understandable to non-compliance audiences - design engineers, product managers, and leadership - and tailor the message to what each audience needs to act on.
  • Self-driven: you take ownership of your projects, work effectively with moderate supervision, and don't wait to be told what needs doing.
  • Courageous: you hold firm on safety and compliance positions under program and schedule pressure, say "no" when the design isn't compliant - and always follow it with the path to "yes."
  • Comfortable in a fast-paced environment with shifting priorities and multiple concurrent programs.
  • A problem-solver who likes to "solve the puzzles" and wants ownership of challenging assignments.
  • Collaborative but decisive: you make sound decisions using all available information, and you can compromise on approach without compromising on safety.

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