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Medical Device Product Development Manager Jobs in Colorado

HIGHRIDGE Inc.

Engineering Project Manager

Westminster, CO · On-site

$90 - $110/hr

Strong working knowledge of medical device product development, including design control, risk management, and quality system requirements.** ** · Demonstrated ability to lead cross-functional teams ...

LivaNova, PLC

Medical Device Assembler

Arvada, CO · On-site

$19.50 - $21/hr

Medical Device Production Assembler Build Products That Help Change Lives Arvada, CO | Full-Time $19.50-$21.00/hour + Annual Bonus + Overtime + Excellent Benefits Looking for stable work, great ...

LivaNova

Medical Device Assembler

Arvada, CO · On-site

$19.50 - $21/hr

Medical Device Production Assembler Build Products That Help Change Lives Arvada, CO | Full-Time $19.50-$21.00/hour + Annual Bonus + Overtime + Excellent Benefits Looking for stable work, great ...

ARTHREX

Sr. Product Manager, Vet Systems

Denver, CO · 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 ...

Quantix

Project Manager

Lakewood, CO · On-site

... 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 ...

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Showing results 1-20

All JobsMedical Device Product Development JobsMedical Device Product Development Manager JobsMedical Device Product Development Manager Jobs in Colorado

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 Sep 5, 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 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 in Colorado are hiring for Medical Device Product Development Manager jobs?

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

Medical Device Product Development Manager jobs near you
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.

Engineering Project Manager

HIGHRIDGE Inc.

Westminster, CO • On-site

$90 - $110/hr

Other

Posted 18 days ago

Job description

Working at Highridge Medical is not just work. Life at Highridge Medical is purpose driven. Every day, you have the privilege of using your talents to demonstrate Confidence in your work and restore Confidence for our patients. Confidence that moves.We are seeking a Project Manager to lead cross-functional teams through the full product development lifecycle, from concept through commercialization within the R&D Department. This role is responsible for project planning, schedule management, risk mitigation, and ensuring compliance with design control and quality system requirements. The NPD Project Manager will partner closely with Engineering, Marketing, Regulatory, Quality, Operations, Clinical, and Supply Chain to deliver innovative spinal implant and instrument solutions on time and within scope. Occasional travel may be required.**Principal Duties and Responsibilities:** **· Facilitates cross-functional collaboration across Engineering, Marketing, Regulatory, Quality, Operations, Clinical, Testing, and Supply Chain to ensure alignment on requirements, deliverables, and timelines.****· Supports the development and refinement of user needs, product requirements, and system specifications by coordinating input from surgeons, marketing, and engineering teams.** **· Coordinates with Regulatory Affairs to ensure project deliverables support global submissions and compliance requirements.** *This is not an exhaustive list of duties or functions and may not necessarily comprise all of the "essential functions" for purposes of the ADA.***Expected Areas of Competence (i.e., knowledge, skills, and abilities):****Strong working knowledge of medical device product development, including design control, risk management, and quality system requirements.** **· Demonstrated ability to lead cross-functional teams and influence without direct authority, consistent with practices at leading device manufacturers.** creativity and ability to take **· Proficiency in developing and managing complex project schedules, resource plans, and risk registers.****· Ability to communicate effectively with technical and non-technical stakeholders, including surgeons, engineers, executives, and external partners.** **· Strong organizational skills with the ability to manage multiple high-complexity projects simultaneously.** **· Experience preparing and delivering executive-level presentations and project status reports.** **· Proficiency with MS Project, Smartsheet, or equivalent project management tools; strong skills in Microsoft Office Suite.****· Familiarity with manufacturing processes, design for manufacturability, and supply chain considerations for implant and instrument systems.** **· Experience in a regulated medical device environment (Class II/III preferred)** **Education/Experience Requirements:****· 3+ years of experience in project management, preferably within the medical device industry or other regulated product development environments.** **· Experience managing cross-functional teams and complex product development projects.** #J-18808-Ljbffr

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