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Medical Product Development Jobs (NOW HIRING)

Coloplast

Product Development Engineer

Minneapolis, MN · On-site

$90K - $120K/yr

The Product Development Engineer at Kerecis is part of a small but seasoned team of medical device professionals responsible for the development and commercialization of the Company's next-generation ...

ARCH Medical Solutions

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Product Development Engineer

Kenosha, WI · On-site

$90K - $110K/yr

The Product Development Engineer designs and develops innovative medical device products, guiding them from initial concept through to market release while ensuring compliance with regulatory and ...

Polyzen, LLC

Product Development Engineer

Apex, NC

... medical device manufacturers. From prototype development through full-scale production, we take ... pride in our quality, technical expertise, and customer service, and we strive to provide the best ...

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How much do medical product development jobs pay per year?

As of Jun 11, 2026, the average yearly pay for medical product development 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 is the highest paid medical trade?

In medical product development, senior roles such as Medical Directors, Regulatory Affairs Directors, and R&D executives tend to have the highest salaries, often exceeding six figures annually. These positions require advanced degrees, extensive experience, and leadership skills, and they typically work in well-funded healthcare or biotech companies.

How to become a medical product rep?

To become a medical product representative, candidates typically need a bachelor's degree in life sciences, healthcare, or business. Relevant skills include knowledge of medical devices, strong communication, and sales abilities; certifications like Certified Medical Sales Professional (CMSP) can enhance prospects. Gaining experience in healthcare or sales and understanding regulatory requirements are also beneficial.

What jobs will boom in 2026?

In the field of medical product development, roles such as biomedical engineers, regulatory affairs specialists, and clinical research coordinators are expected to grow due to advances in healthcare technology and increased demand for innovative medical devices. Skills in data analysis, regulatory compliance, and familiarity with medical standards will be valuable for these positions. The industry will also see increased opportunities for professionals with expertise in digital health and medical software development.

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

To excel in Medical Product Development, you need a background in biomedical engineering, life sciences, or a related field, along with experience in product design and regulatory compliance. Familiarity with CAD software, quality management systems (QMS), and ISO or FDA regulatory standards is typically required. Strong project management, problem-solving abilities, and effective cross-functional communication are crucial soft skills for this role. These competencies ensure the creation of safe, innovative medical products that meet regulatory requirements and address patient needs.

What is medical product development?

Medical product development involves designing, testing, and bringing medical devices or pharmaceuticals to market. Professionals in this field often work with regulatory standards, clinical trials, and engineering tools to ensure safety and efficacy of new products.

What are some common challenges faced in Medical Product Development, and how can professionals effectively navigate them?

Professionals in Medical Product Development often encounter challenges such as navigating complex regulatory requirements, coordinating cross-functional teams, and managing tight project timelines. Success in this role requires strong project management skills, adaptability, and effective communication with stakeholders including engineers, clinicians, and regulatory experts. Building a thorough understanding of FDA or international guidelines, maintaining meticulous documentation, and fostering collaborative team environments can help overcome these obstacles and drive successful product launches.
More about Medical Product Development jobs
What cities are hiring for Medical Product Development jobs? Cities with the most Medical Product Development job openings:
What states have the most Medical Product Development jobs? States with the most job openings for Medical Product Development jobs include:
Medical Product Development jobs near you
Infographic showing various Medical Product Development job openings in the United States as of June 2026, with employment types broken down into 2% As Needed, 80% Full Time, 15% Part Time, 1% Temporary, 1% Contract, and 1% Nights. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $126,987 per year, or $61.1 per hour.
Product Development Engineer

Product Development Engineer

Comfort Medical

Minneapolis, MN • On-site

$90K - $120K/yr

Other

Posted 5 days ago

Job description

The Product Development Engineer at Kerecis is part of a small but seasoned team of medical device professionals responsible for the development and commercialization of the Company's next-generation products across its wound, burn and surgery market. This position will include laboratory work and interacting with suppliers.

The Product Development Engineer is based at the Minneapolis, Minnesota, facility and reports to the Director of Research & Product Development.  This is a full-time in office position.

Major Areas of Accountability

  • Apply core engineering principles to support the development and testing of new product and technology concepts through the company's stage-gate process, under guidance from project tech leads
  • Maintain accurate and detailed documentation throughout all phases of product development
  • Contribute technical content for regulatory submissions (e.g., 510(k), IDE, CE marking) with oversight
  • Collaborate with Quality, Regulatory, and Manufacturing teams to ensure design outputs meet compliance, usability, and manufacturability requirements
  • Support the translation of customer and clinical needs into design inputs and product specifications
  • Assist with process development, scale-up, and technology transfer activities in collaboration with manufacturing and development leads
  • Participate in risk management activities, including hazard identification, analysis, and documentation
  • Design, perform, and document laboratory experiments, methods development, and product testing with defined objectives
  • Support verification and validation (V&V) activities, including test execution and reporting
  • Conduct product feasibility and pre-clinical tests in-house and assist with outsourcing activities to third-party facilities, including preparation of protocols, data collection forms, and draft reports
  • Communicate project status and technical results in team and project meetings
  • Support monitoring of emerging technologies and manufacturing processes relevant to current projects
  • Kerecis employees are required to conduct business to the highest ethical and professional standards; comply with applicable laws and regulations, the Advamed Code of Ethics on Interactions with Healthcare Professionals, and company policies
  • Other job duties as assigned

Basic Qualifications

  • Bachelor's degree in Biomedical, Mechanical or Chemical Engineering or equivalent
  • 3+ years of full-time experience in a product development role within the medical device industry
  • Experience working in FDA- and/or ISO-regulated medical product development environments
  • Experience supporting verification and validation testing, including execution and documentation
  • Familiarity with design of experiments, test method development, basic statistical analysis, and data analysis tools

Preferred Qualifications

  • Solid foundation in engineering principles; exposure to biomaterials, wound dressings, or tissue regeneration is a plus

Base Salary Range: $90,000 - $120,000

This job description is intended to set forth the core functions required for this position and describe the general nature of the work to be performed. It may not contain a comprehensive inventory of all duties, responsibilities, and qualifications required of employees to do this job. Job duties, responsibilities and activities may change or be supplemented at any time as necessary. Kerecis is an Equal Opportunity Employer.

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