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Biocompatibility Scientist Jobs (NOW HIRING)

Stryker

Principal Specialist, Regulatory Science

Orlando, FL · On-site +1

$143K - $238K/yr

Remote Stryker is seeking a Principal Specialist, Regulatory/Clinical Science (Biocompatibility & Sterility) for our Orthopedic Technologies Division | Mako & Enabling Technologies. This is a remote ...

Cellanome

Staff Scientist, Chemistry

Foster City, CA

$140K - $200K/yr

Cellanome is seeking an experienced chemist or materials scientist to advance the development and ... Experience with biocompatibility evaluation of biomaterials. The estimated base salary range for ...

Subsense

Research Scientist in Neuroscience

Palo Alto, CA · On-site

$115K - $140K/yr

The Opportunity We're seeking a Research Scientist with strong expertise in neuroscience laboratory ... Perform biocompatibility experiments, as well as live fluorescence and electrophysiology research ...

Tunnell Government Services

Toxicologist

Bethesda, MD · On-site

This candidate must serve as a technical authority in the scientific analysis of the safety and ... Basics of Biocompatibility: Information Needed for Assessment by the FDA (website) * Standards:

Cellanome

Staff Scientist, Chemistry

Foster City, CA · On-site

$140K - $200K/yr

We're amassing a world class team of engineers, scientists, team builders and problem solvers to ... Experience with biocompatibility evaluation of biomaterials. The estimated base salary range for ...

Medline

Principal Toxicologist

Northfield, IL · On-site +1

$152K - $229K/yr

... biocompatibility testing under GLP requirements. * Serve as a subject matter expert, providing strategic guidance and scientific expertise to cross-functional teams, including R&D, quality, and ...

Medline

Principal Toxicologist

Northfield, IL · On-site

$152K - $229K/yr

... biocompatibility testing under GLP requirements. * Serve as a subject matter expert, providing strategic guidance and scientific expertise to cross-functional teams, including R&D, quality, and ...

Tunnell Government Services

Toxicologist

Bethesda, MD · On-site

Tunnell Government Services, Inc., is comprised of the industry's leading scientists, medical and ... Basics of Biocompatibility: Information Needed for Assessment by the FDA (website) * Standards:

Medline

Principal Toxicologist

Northfield, IL

$152K - $229K/yr

... biocompatibility testing under GLP requirements. * Serve as a subject matter expert, providing strategic guidance and scientific expertise to cross-functional teams, including R&D, quality, and ...

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Biocompatibility Scientist information

What types of projects and collaborations are common for Biocompatibility Scientists in a typical work setting?

Biocompatibility Scientists often work on projects that evaluate the safety of medical devices, materials, or pharmaceuticals by designing and conducting biological tests. They regularly collaborate with R&D, regulatory affairs, quality assurance, and clinical research teams to interpret results and prepare documentation for regulatory submissions. Daily responsibilities may include running laboratory assays, analyzing data, writing technical reports, and presenting findings in cross-functional meetings. Close interaction with project managers and engineers is common to ensure testing aligns with product development timelines and compliance requirements. This multidisciplinary environment provides excellent opportunities to broaden expertise and advance into leadership or regulatory strategy roles.

What does a Biocompatibility Scientist do?

A Biocompatibility Scientist evaluates the compatibility of medical devices, biomaterials, and pharmaceuticals with biological systems to ensure safety and regulatory compliance. They conduct risk assessments, review toxicological data, and design biocompatibility testing strategies following international standards like ISO 10993. Their work involves collaborating with regulatory bodies, R&D teams, and quality assurance to ensure products meet health and safety requirements before market release.

What are the key skills and qualifications needed to thrive in the Biocompatibility Scientist position, and why are they important?

To thrive as a Biocompatibility Scientist, you need a strong background in biology, chemistry, or biomedical engineering, typically supported by an advanced degree and experience with regulatory standards like ISO 10993. Expertise with laboratory analytical techniques (such as cytotoxicity, sensitization assays), data analysis software, and familiarity with submission processes for agencies like the FDA or EMA are highly valued. Strong attention to detail, effective communication, and collaboration skills are essential for working in multidisciplinary teams and documenting findings clearly. These competencies ensure the safety and compliance of medical devices or materials, which is critical for successful product development and regulatory approval.

More about Biocompatibility Scientist jobs
What are the most commonly searched types of Biocompatibility Scientist jobs? The most popular types of Biocompatibility Scientist jobs are:
What job categories do people searching Biocompatibility Scientist jobs look for? The top searched job categories for Biocompatibility Scientist jobs are:
Biocompatibility Scientist jobs near you
Infographic showing various Biocompatibility Scientist job openings in the United States as of May 2026, with employment types broken down into 88% Full Time, 6% Temporary, and 6% Contract. Highlights an 94% In-person, and 6% Remote job distribution.
Principal Specialist, Regulatory Science

Principal Specialist, Regulatory Science

Stryker

Orlando, FL • On-site

$143K - $238K/yr

Full-time

Posted 6 days ago

Job description

Work Flexibility: Remote
Stryker is seeking a Principal Specialist, Regulatory/Clinical Science (Biocompatibility & Sterility) for our Orthopedic Technologies Division | Mako & Enabling Technologies. This is a remote position based in the Eastern Time Zone.
As the Principal Specialist, Regulatory Science, you will provide both strategic direction and hands-on technical leadership in biocompatibility and sterility, ensuring consistent, compliant, and scalable practices across product development and sustaining activities. You will operate as a senior individual contributor driving alignment, standards, and execution across the business.
What You Will Do
  • Define and implement Clinical Sciences strategies for biocompatibility and sterility across new product development and sustaining programs
  • Lead development of quality system frameworks, standards, and processes to support compliant clinical science practices
  • Own and deliver clinical sciences work products, including test strategies, risk assessments, and regulatory documentation
  • Provide technical leadership on biocompatibility evaluations (ISO 10993), sterilization validation (e.g., EO, radiation), and microbiological risk
  • Integrate clinical science strategies with risk management and design controls to ensure alignment across product lifecycle stages
  • Identify and implement process improvements, standardization, and tools to enhance efficiency, reduce rework, and improve quality outcomes
  • Partner with cross-functional teams to influence program decisions, resolve technical challenges, and maintain execution timelines
  • Mentor team members and contribute to building scalable capabilities through development of best practices and technical frameworks

What You Need
Required
  • Bachelor's degree in Biomedical Engineering, Biology, Microbiology, Materials Science, or related field
  • Minimum 10 years of experience in the medical device industry with focus on biocompatibility and/or sterility
  • Demonstrated expertise in ISO 10993 biocompatibility standards and sterilization validation methods
  • Experience applying ISO 14971 risk management principles within product development

Preferred
  • Advanced degree (Master's or PhD) in a related scientific discipline
  • Experience supporting orthopedic, robotic, or implantable medical device products
  • Experience supporting regulatory submissions, audits, or inspections
  • Experience developing or scaling technical functions, frameworks, or processes

United States of America Pay Ranges:
  • Puerto Rico: $102,600 - $171,000 USD Annual
  • USN: $110,100 - $183,400 USD Annual
  • US5: $115,600 - $192,600 USD Annual
  • US10: $121,100 - $201,700 USD Annual
  • US15: $126,600 - $210,900 USD Annual
  • US20: $132,100 - $220,100 USD Annual
  • US30: $143,100 - $238,400 USD Annual

View the U.S. work location and transparency guide to find the pay range for your location.
Travel Percentage: 10%
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.
Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information.

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