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Medical Device Product Development Manager Jobs in Colorado

Medical Device Engineer

Aurora, CO ยท Hybrid

$57.69/hr

... support product development activities, electrical safety testing, risk management efforts, and ... Support compliance efforts related to EU Medical Device Regulation (EU MDR 2017/745). * Develop ...

Sr. Product Manager, Vet Systems

Denver, CO ยท On-site

$130K - $171K/yr

Requisition ID: 65189 Title: Sr. Product Manager, Vet Systems Arthrex, Inc. is a global medical device company and a leader in new product development and medical education within the orthopedic ...

Ability to learn advanced assembly skills and product flow process * Ability to reliably interpret ... medical devices. We hire individuals who are looking for more than just a job. Every role at our ...

... top medical device / services companies in the world, providing life saving products to their ... development / engineering. 3) PMP certification. Desired Skills: 1) FDA or other regulatory ...

Medical Device Assembler

Arvada, CO ยท On-site

$19.50 - $21/hr

Ability to learn advanced assembly skills and product flow process * Ability to reliably interpret ... medical devices. We hire individuals who are looking for more than just a job. Every role at our ...

Medical Device Assembler

Arvada, CO ยท On-site

$19.50 - $21/hr

Ability to learn advanced assembly skills and product flow process * Ability to reliably interpret ... medical devices. We hire individuals who are looking for more than just a job. Every role at our ...

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Showing results 1-20

Medical Device Product Development Manager information

See Colorado salary details

$37.5K

$119.5K

$136.6K

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

As of Aug 11, 2026, the average yearly pay for medical device product development manager in Colorado is $119,512.00, according to ZipRecruiter salary data. Most workers in this role earn between $108,200.00 and $135,700.00 per year, depending on experience, location, and employer.

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.

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 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 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.
What cities in Colorado are hiring for Medical Device Product Development Manager jobs? Cities in Colorado with the most Medical Device Product Development Manager job openings:
Infographic showing various Medical Device Product Development Manager job openings in Colorado 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 $119,512 per year, or $57.5 per hour.

Medical Device Engineer

Actalent

Aurora, CO โ€ข Hybrid

$57.69/hr

Contractor

Medical, Dental, Vision, Life, Retirement, PTO

This job post hasย expired 1 day ago.ย Applications are no longer accepted.


Job description

Job Title: Electrical Engineer

Job Description

We're seeking an experienced Electrical Engineer to join a team focused on the development, testing, and regulatory compliance of innovative medical devices. In this role, you'll play a critical part in ensuring products meet global safety and performance standards while helping bring life-changing technologies to market.

This position offers a unique opportunity to work at the intersection of engineering, product development, quality, and regulatory compliance. You'll collaborate with cross-functional teams to support product development activities, electrical safety testing, risk management efforts, and regulatory initiatives, including compliance with EU MDR and IEC 60601 standards.


What You'll Do

As an Electrical Engineer, you will:

  • Design, evaluate, and support electrical systems used in medical devices.
  • Plan, execute, and document electrical safety testing in accordance with IEC 60601 standards.
  • Support compliance efforts related to EU Medical Device Regulation (EU MDR 2017/745).
  • Develop technical documentation required for product development and regulatory submissions.
  • Partner with Quality, Regulatory Affairs, Manufacturing, and R&D teams throughout the product lifecycle.
  • Support risk management activities in accordance with ISO 14971 methodologies.
  • Participate in design reviews, verification activities, and product investigations.
  • Work with third-party testing laboratories and certification organizations during compliance testing.
  • Analyze product issues and implement effective corrective actions.
  • Assist with audit readiness and regulatory inspections.

Required Qualifications
  • Bachelor's degree in Electrical Engineering or a related engineering discipline.
  • Experience supporting medical device development or work within a highly regulated industry.
  • Strong understanding of electrical design principles and product development processes.
  • Experience supporting or executing testing to IEC 60601 standards.
  • Knowledge of EU MDR requirements and medical device compliance activities.
  • Experience with electrical safety testing equipment and laboratory environments.
  • Familiarity with design controls, engineering documentation, and quality systems.
  • Strong analytical, troubleshooting, and problem-solving skills.
  • Excellent communication and collaboration abilities.

Preferred Experience

Candidates with any of the following will stand out:

  • IEC 60601-1-2 EMC testing experience.
  • CE Marking support for medical devices.
  • Knowledge of FDA medical device regulations.
  • Experience with ISO 13485 quality systems.
  • Experience facilitating risk management activities under ISO 14971.
  • Verification and validation testing experience.
  • Embedded systems, power electronics, or medical device software integration experience.
  • Direct interaction with Notified Bodies or third-party compliance laboratories.

Technologies & Standards

You may work with:

  • EU MDR (2017/745)
  • IEC 60601-1 Electrical Safety Standards
  • IEC 60601-1-2 EMC Standards
  • ISO 13485 Quality Systems
  • ISO 14971 Risk Management
  • Design Controls & Technical Documentation
  • Electrical Safety Testing Equipment

Why Join Us?
  • Help deliver safe and compliant medical devices that impact patient outcomes worldwide.
  • Collaborate with experienced engineering, regulatory, and quality teams.
  • Gain exposure to global regulatory requirements and advanced medical technologies.
  • Work on challenging projects involving product safety, compliance, and innovation.
  • Influence products from development through commercialization and regulatory approval.

Job Type & Location

This is a Contract position based out of Centennial, CO.

Pay and Benefits

The pay range for this position is $57.69 - $57.69/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a hybrid position in Centennial,CO.

Application Deadline

This position is anticipated to close on Aug 5, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.


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About Actalent

Sourced by ZipRecruiter

Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We're supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.

Company size

5,001 - 10,000 Employees

Headquarters location

Hanover, MD, US

Year founded

1983

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