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Biocompatibility Jobs (NOW HIRING)

millenniumsoft

NC · On-site

This position works as a member of the biology group and is responsible for biocompatibility testing on medical devices and materials. * Testing is performed in a corporate lab that performs ...

Critical Innovations

Preclinical Scientist

Lawndale, CA · On-site +1

... biocompatibility, bench performance, and other translational studies. Most studies are expected to be performed off-site through external Contract Research Organizations (CROs), testing laboratories ...

Philips

Senior Biological Safety Engineer

Murrysville, PA · On-site

$102K - $163K/yr

Developing and conducting biocompatibility training programs, work within a team environment to peer-review deliverables, and provide clear, consistent weekly project status updates to stakeholders.

Tunnell Government Services

Toxicologist

Bethesda, MD · On-site

FDA Biocompatibility Guidance LINK * Basics of Biocompatibility: Information Needed for Assessment by the FDA (website) * Standards: * ISO 10993-1:2018, Biological evaluation of medical devices ...

Bausch+Lomb Companies Inc.

$150K - $200K/yr

Manage team responsible for medical device biocompatibility support * Responsible for project strategies, risk assessments, biocompatibility evaluation plans and reports for medical devices * Ensures ...

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Biocompatibility information

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$41K

$115.4K

$214K

How much do biocompatibility jobs pay per year?

As of May 30, 2026, the average yearly pay for biocompatibility in the United States is $115,369.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,000.00 and $135,500.00 per year, depending on experience, location, and employer.

What is a Biocompatibility job?

A Biocompatibility job involves evaluating medical devices, materials, and implants to ensure they are safe and non-toxic for human use. Professionals in this role analyze the interactions between biomaterials and biological systems, conducting risk assessments and regulatory compliance reviews. They work closely with engineers, scientists, and regulatory teams to meet standards like ISO 10993. This job is critical in ensuring patient safety and securing product approvals for medical devices.

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

To thrive in a Biocompatibility role, you typically need a background in biomedical engineering, materials science, or a related life science field, with strong knowledge of biological safety and regulatory requirements for medical devices. Familiarity with ISO 10993 standards, biocompatibility testing methods, and data analysis tools is essential, along with potential certification in regulatory affairs or toxicology. Attention to detail, effective communication, and problem-solving abilities are vital soft skills for collaborating across multidisciplinary teams. These skills ensure accurate safety evaluations and regulatory compliance, which are crucial for bringing safe and effective medical products to market.

What are typical daily responsibilities for someone working in Biocompatibility?

Professionals in Biocompatibility routinely assess the biological safety of new materials or devices, design or coordinate laboratory tests, and analyze results to determine compliance with regulatory standards. Their day-to-day work often involves preparing technical reports, collaborating with R&D and regulatory teams, and communicating findings to project stakeholders. You may also contribute to risk assessments, provide input during product development stages, and stay updated on evolving international regulations. This role requires balancing technical expertise with proactive communication to ensure the safe and timely approval of medical products.
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What cities are hiring for Biocompatibility jobs? Cities with the most Biocompatibility job openings:
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Biocompatibility jobs near you
Infographic showing various Biocompatibility job openings in the United States as of May 2026, with employment types broken down into 98% Full Time, and 2% Contract. Highlights an 95% Physical, and 5% Remote job distribution, with an average salary of $115,369 per year, or $55.5 per hour.
Manufacturing Engineer

Manufacturing Engineer

Alexander Technology Group

Stratham, NH • On-site

$76.80K - $98.90K/yr

Other

This job post has expired today. Applications are no longer accepted.

Job description

Alexander Technology Group is looking for Principal Mechanical Engineer to lead the design and development of mechanical components for drug-device combination products, including material selection, biocompatibility, E&L, and human factors integration. Drive DFM/DFA, risk management (ISO 14971), and compliance with FDA/ISO standards.


Qualifications & Experience

  • BS in Mechanical, Materials Engineering, or related field (MS/PhD preferred)
  • 12+ years of mechanical product development experience, including 7+ years in medical devices or combination products
  • Strong expertise in drug-device systems, E&L, biocompatibility (ISO 10993), and human factors engineering
  • Deep knowledge of ISO 13485, ISO 14971, 21 CFR Part 820/Part 4, ISO 11608, and cGMP
  • Experience leading IQ/OQ/PQ validations, design controls, FEA, tolerance analysis, and SPC
  • Proficiency in SolidWorks and PDM/PLM systems


If interested, please send resume to Jpolombo@alexandertg.com

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