ZipRecruiter

Log In

1

Director Biomaterials Engineer Jobs (NOW HIRING)

Coloplast

Product Development Engineer

Minneapolis, MN · On-site

$90K - $120K/yr

... and reports to the Director of Research & Product Development. This is a full-time in office ... Solid foundation in engineering principles; exposure to biomaterials, wound dressings, or tissue ...

Danone

Packaging Director, Food & Beverage

Louisville, CO · Hybrid

$146K - $210K/yr

Build futureready competencies in areas such as: * advanced materials , biomaterials, barrier ... Lead and grow a highperforming team of 5+ packaging engineers and managers, fostering curiosity ...

Werfen

Director of Product Quality

San Diego, CA · On-site

... biomaterials. We operate directly in 30 countries, and in more than 100 territories through ... Lead, develop, and mentor the Product Quality organization, including Quality Engineering for new ...

Werfen

Systems Engineer III

Bedford, MA · On-site

$90K - $120K/yr

... biomaterials. We operate directly in 30 countries, and in more than 100 territories through ... direct people management responsibility * Experience working in a regulated medical device, in ...

Danone

Packaging Director, Food & Beverage

Louisville, CO · Hybrid

$146K - $210K/yr

Build futureready competencies in areas such as: * advanced materials , biomaterials, barrier ... Lead and grow a highperforming team of 5+ packaging engineers and managers, fostering curiosity ...

Werfen

Director of Product Quality

San Diego, CA · On-site

... biomaterials. We operate directly in 30 countries, and in more than 100 territories through ... Lead, develop, and mentor the Product Quality organization, including Quality Engineering for new ...

Werfen

Director of Product Quality

San Diego, CA

... biomaterials. We operate directly in 30 countries, and in more than 100 territories through ... Lead, develop, and mentor the Product Quality organization, including Quality Engineering for new ...

Werfen

Systems Engineer III

Bedford, MA · On-site

$90K - $120K/yr

... biomaterials. We operate directly in 30 countries, and in more than 100 territories through ... direct people management responsibility * Experience working in a regulated medical device, in ...

Werfen

Systems Engineer III

Bedford, MA · On-site

$90K - $120K/yr

... biomaterials. We operate directly in 30 countries, and in more than 100 territories through ... direct people management responsibility * Experience working in a regulated medical device, in ...

Werfen

Director of Product Quality

San Diego, CA

... biomaterials. We operate directly in 30 countries, and in more than 100 territories through ... Lead, develop, and mentor the Product Quality organization, including Quality Engineering for new ...

Werfen

Director of Product Quality

San Diego, CA · On-site

... biomaterials. We operate directly in 30 countries, and in more than 100 territories through ... Lead, develop, and mentor the Product Quality organization, including Quality Engineering for new ...

Werfen

Systems Engineer III

Bedford, MA

$90K - $120K/yr

... biomaterials. We operate directly in 30 countries, and in more than 100 territories through ... direct people management responsibility * Experience working in a regulated medical device, in ...

next page

Showing results 1-20

All JobsDirector Biomaterials Engineer Jobs

Director Biomaterials Engineer information

See salary details

$73K

$194.7K

$254K

How much do director biomaterials engineer jobs pay per year?

As of Jul 2, 2026, the average yearly pay for director biomaterials engineer in the United States is $194,709.00, according to ZipRecruiter salary data. Most workers in this role earn between $141,500.00 and $253,000.00 per year, depending on experience, location, and employer.

What does a Director Biomaterials Engineer do?

A Director Biomaterials Engineer leads teams in the research, development, and implementation of new materials designed to interact with biological systems. They oversee projects involving medical devices, implants, or tissue engineering, ensuring that materials are safe, effective, and meet regulatory standards. This role involves collaborating with scientists, engineers, and regulatory professionals, as well as managing budgets and strategic planning for biomaterials initiatives. Directors also play a key role in guiding innovation and ensuring products meet both commercial and clinical needs.

What are the key skills and qualifications needed to thrive as a Director Biomaterials Engineer, and why are they important?

To thrive as a Director Biomaterials Engineer, you need deep expertise in materials science, biomedical engineering, and project management, typically supported by an advanced degree (PhD or MS) and significant industry experience. Familiarity with laboratory instrumentation, biomaterial characterization techniques, regulatory standards (such as FDA or ISO), and often CAD or simulation software is essential. Strong leadership, strategic thinking, and effective communication are vital soft skills for guiding teams and collaborating with cross-functional stakeholders. These competencies ensure innovative product development, regulatory compliance, and successful commercialization in the biomedical field.

What are the typical leadership responsibilities for a Director Biomaterials Engineer, and how does this role interact with cross-functional teams?

As a Director Biomaterials Engineer, you'll be responsible for guiding a team of scientists and engineers in the research, development, and optimization of biomaterial products. In addition to overseeing technical projects, you'll collaborate closely with departments such as regulatory affairs, manufacturing, and product management to ensure alignment on project goals and compliance requirements. Regular meetings with cross-functional teams are common, and you'll often serve as the primary technical liaison, translating complex biomaterials concepts for non-technical stakeholders. Effective leadership, communication, and strategic planning are key to success in this role.

What is the difference between Director Biomaterials Engineer vs Biomaterials Engineer?

AspectDirector Biomaterials EngineerBiomaterials Engineer
CredentialsBachelor's/Master's/PhD in biomedical engineering or materials science, leadership experienceBachelor's/Master's in biomedical engineering or related field
Work EnvironmentLeadership roles in R&D, product development, strategic planningDesign, testing, and development of biomaterials in labs or manufacturing
Employer & IndustryMedical device companies, biotech firms, research institutionsResearch labs, manufacturing plants, biotech companies

The main difference is that the Director Biomaterials Engineer oversees teams and strategic projects, while the Biomaterials Engineer focuses on hands-on research and development. The director has more leadership responsibilities, whereas the engineer is more involved in technical tasks.

More about Director Biomaterials Engineer jobs
What cities are hiring for Director Biomaterials Engineer jobs? Cities with the most Director Biomaterials Engineer job openings:
What are the most commonly searched types of Biomaterials Engineer jobs? The most popular types of Biomaterials Engineer jobs are:
What states have the most Director Biomaterials Engineer jobs? States with the most job openings for Director Biomaterials Engineer jobs include:
What job categories do people searching Director Biomaterials Engineer jobs look for? The top searched job categories for Director Biomaterials Engineer jobs are:
Director Biomaterials Engineer jobs near you
Infographic showing various Director Biomaterials Engineer job openings in the United States as of June 2026, with employment types broken down into 85% Full Time, 13% Part Time, and 2% Contract. Highlights an 89% Physical, 4% Hybrid, and 7% Remote job distribution, with an average salary of $194,709 per year, or $93.6 per hour.
Product Development Engineer

Product Development Engineer

Comfort Medical

Minneapolis, MN

$90K - $120K/yr

Other

Posted 26 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.

60252
#LI-KR

Apply