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Medical Device Product Development Jobs in Colorado

Sr Electrical Engineer

Lafayette, CO · On-site

$111K - $145K/yr

Medical device product development. * Hardware reliability engineering. * Component obsolescence management. * Cross-functional collaboration with software, mechanical, manufacturing, and quality ...

Sr. Product Manager, Vet Systems

Denver, CO

$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 ...

Medical Device Assembler

Arvada, CO · 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 ...

Direct and guide employees in the design and development of medical device products and systems. * Develop, implement, and continuously improve objectives, policies, processes, and standards to ...

Product Engineer II (Manufacturing Engineer II - Medical Device) This role focuses on supporting a high-volume medical device manufacturing line by providing hands-on production support ...

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Showing results 1-20

Medical Device Product Development information

See Colorado salary details

$44.7K

$133.5K

$151.9K

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

As of Jul 29, 2026, the average yearly pay for medical device product development in Colorado is $133,530.00, according to ZipRecruiter salary data. Most workers in this role earn between $120,400.00 and $150,400.00 per year, depending on experience, location, and employer.

What is a Medical Device Product Development job?

A Medical Device Product Development job involves designing, testing, and bringing medical devices to market while ensuring compliance with regulatory standards. Professionals in this role work with cross-functional teams, including engineering, regulatory affairs, and manufacturing, to develop safe and effective healthcare solutions. They oversee the entire product lifecycle, from concept and prototyping to clinical validation and commercialization. Strong knowledge of FDA, ISO, and other regulatory requirements is essential.

What are some typical challenges faced in Medical Device Product Development roles?

Professionals in Medical Device Product Development often encounter challenges such as navigating complex regulatory requirements, managing cross-functional project teams, and ensuring that products meet both clinical needs and quality standards. Balancing innovative design with safety and compliance can require careful planning and solid problem-solving skills. Additionally, adapting to shifting project timelines and incorporating stakeholder feedback are common aspects of the job. Overcoming these challenges is rewarding and helps ensure the delivery of safe, effective devices to patients and healthcare providers.

What are the key skills and qualifications needed to thrive in the Medical Device Product Development position, and why are they important?

To thrive in Medical Device Product Development, you need a strong background in engineering or life sciences, product design, and an understanding of regulatory requirements like FDA and ISO standards. Proficiency with CAD software, project management tools, and knowledge of quality management systems (QMS) is commonly required, along with certifications such as Six Sigma or PMP being beneficial. Strong problem-solving abilities, collaboration skills, and effective communication are key soft skills for this role. These skills are important to ensure that devices are developed safely, efficiently, and in compliance with industry regulations while fostering innovation and teamwork.

What are the most commonly searched types of Medical Device Product Development jobs in Colorado? The most popular types of Medical Device Product Development jobs in Colorado are:
What are popular job titles related to Medical Device Product Development jobs in Colorado? For Medical Device Product Development jobs in Colorado, the most frequently searched job titles are:
What job categories do people searching Medical Device Product Development jobs in Colorado look for? The top searched job categories for Medical Device Product Development jobs in Colorado are:
What cities in Colorado are hiring for Medical Device Product Development jobs? Cities in Colorado with the most Medical Device Product Development job openings:
Infographic showing various Medical Device Product Development job openings in Colorado as of July 2026, with employment types broken down into 57% Full Time, and 43% Contract. Highlights an 100% In-person job distribution, with an average salary of $133,530 per year, or $64.2 per hour.

Engineering Project Manager

Highridge Medical

Westminster, CO

Full-time

Posted 13 days ago


Job description

Engineering Project Manager

Highridge Medical creates the world's most innovative spinal solutions across the spectrum from Motion Preservation to Minimally Invasive Surgeryto Core Spine.

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 todemonstrateConfidence in your work and restore Confidence for our patients. Confidence that moves.

JobSummary:

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 roleis responsible forproject 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 berequired.

Principal Duties and Responsibilities:

Leads the planning of new product development projects using structured phase-gate and design control processes common to the medical device industry.

Develops andmaintainsdetailed Gantt charts, project schedules, resource plans, and critical path analyses.

Facilitatescross-functional collaboration across Engineering, Marketing, Regulatory, Quality, Operations, Clinical, Testing, and Supply Chain to ensure alignment on requirements, deliverables, and timelines.

Leads project meetings, including kickoffs, weekly status reviews, technical reviews, and phase-gate approvals; prepares agendas, documents minutes, assigns action items, and drives accountability.

Tracks project progress,identifiesrisks, and implements mitigation strategies to ensure successful execution.

Supports the completion of project documentation that isaccurate, and compliant within the Design History File (DHF).

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.

Works with Operations and Supply Chain to support manufacturing readiness, pilot builds, process validation, and launch planning.

Prepares and presents project updates, dashboards, and risk assessments to leadership and executive stakeholders.

Manages multiple concurrent projects and adjusts plans to meet evolving business priorities.

This is not an exhaustive list of duties or functions and may not necessarilycompriseall ofthe "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.

Demonstratedability to lead cross-functional teams and influence without direct authority, consistent with practices at leading device manufacturers.

Demonstratedcreativity and ability to takeactionsin solving problems and making decisions in a dynamic and evolving environment.

Proficiencyin 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.

Proficiencywith 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:

MinimumB.S. degree in Engineering, Project Management, Business, or related field.

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.

PMP certification or equivalent is a plus.

Please visit Highridgemedical.com foradditionalinformation.

Highridge Medical is an equal opportunity employer committed to diversity and inclusion in the workplace. All qualified applicants for employment and employment decisionsareconsidered and evaluated without regard to race, color, religion, religious beliefs, creed, national origin, ancestry, citizenship status, age, gender, sex (including pregnancy, childbirth, related medical conditions, lactation and breastfeeding), gender identity or expression (including transgender status), sexual orientation, marital status, military status,protected veteran status, disability, protected medical condition as defined by applicable state or local law, genetic information, or any other status protected under applicable federal, state, and local laws.