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Biocompatibility Engineer Jobs (NOW HIRING)

Managed Staffing

Biocompatibility Scientist

FL · Remote

$145 - $150/hr

D. in Biology, Biomedical Engineering, Toxicology, Materials Science, or related field. * Strong ... biocompatibility assessments for medical devices. * Proven ability to interpret scientific data ...

AbbVie

Scientist II - Biocompatibility

Branchburg, NJ · On-site

The Scientist II - Biocompatibility is a SME which will provide highly skilled support for ... Bachelor's Degree in Life Science/Biomedical Engineering or related field with minimal 7 years of ...

AbbVie

Scientist II - Biocompatibility

Branchburg, NJ · On-site

$78K/yr

The Scientist II - Biocompatibility is a SME which will provide highly skilled support for ... Bachelor's Degree in Life Science/Biomedical Engineering or related field with minimal 7 years of ...

AbbVie

Scientist II - Biocompatibility

Branchburg, NJ · On-site

The Scientist II - Biocompatibility is a SME which will provide highly skilled support for ... Bachelor's Degree in Life Science/Biomedical Engineering or related field with minimal 7 years of ...

Marmon

Biocompatibility Program Manager

Addison, TX

Bachelor's degree in biological or physical sciences, or engineering * Preferred: advanced education in toxicology or microbiology * Minimum 5years ofexperience applying biocompatibility (surgically ...

Philips

Senior Biological Safety Engineer

Murrysville, PA · On-site

$102K - $163K/yr

Job Title Senior Biological Safety Engineer Your role: * Working collaboratively with cross ... Developing and conducting biocompatibility training programs, work within a team environment to ...

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How much do biocompatibility engineer jobs pay per year?

As of Jun 5, 2026, the average yearly pay for biocompatibility engineer in the United States is $89,183.00, according to ZipRecruiter salary data. Most workers in this role earn between $66,500.00 and $109,000.00 per year, depending on experience, location, and employer.

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

To thrive as a Biocompatibility Engineer, you need a strong background in biomedical engineering or life sciences, with expertise in toxicology, materials science, and regulatory standards such as ISO 10993. Familiarity with laboratory testing protocols, risk assessment tools, and regulatory submission systems is typically required, and certifications like Certified Biological Safety Professional (CBSP) can be advantageous. Strong analytical thinking, meticulous attention to detail, and effective communication skills help in interpreting data, preparing reports, and collaborating with cross-functional teams. These competencies are crucial for ensuring medical devices are safe for human use and meet global compliance requirements.

What are some common challenges faced by Biocompatibility Engineers during the device development process?

Biocompatibility Engineers often encounter challenges in selecting appropriate materials that meet regulatory standards and ensuring compatibility with biological systems. They must navigate complex testing protocols and documentation requirements to demonstrate safety and effectiveness, which can be time-consuming and require cross-functional collaboration with regulatory, quality, and R&D teams. Additionally, staying updated with evolving international regulations and standards is vital, as non-compliance can delay product approvals and market entry.

What does a Biocompatibility Engineer do?

A Biocompatibility Engineer is responsible for evaluating and ensuring that materials and devices intended for medical use are safe and compatible with biological systems. Their work involves assessing the interactions between medical devices and human tissues to prevent adverse reactions. They conduct laboratory tests, analyze data, and prepare technical documentation to meet regulatory standards. Biocompatibility Engineers play a crucial role in the development and approval of medical devices, working closely with regulatory agencies and product development teams.

What is the difference between Biocompatibility Engineer vs Materials Scientist?

AspectBiocompatibility EngineerMaterials Scientist
Required CredentialsBachelor's or Master's in biomedical engineering, biology, or related fields; certifications in biocompatibility testingBachelor's or Master's in materials science, chemistry, or engineering; advanced degrees often preferred
Work EnvironmentMedical device companies, research labs, regulatory agenciesResearch institutions, manufacturing, aerospace, automotive industries
Industry UsageDesign and testing of biocompatible medical devices and implantsDevelopment of new materials for various applications, including medical, industrial, and consumer products

While both roles involve materials and testing, a Biocompatibility Engineer specializes in ensuring materials are safe for medical use, focusing on biological interactions. A Materials Scientist has a broader scope, working on developing and analyzing materials across multiple industries. The two roles often collaborate but serve distinct functions within product development and safety assurance.

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Biocompatibility Engineer jobs near you
Biocompatibility Scientist

Biocompatibility Scientist

Managed Staffing

FL • Remote

$145 - $150/hr

Contractor

Posted 2 days ago

Job description

Biocompatibility Scientist (100% Remote)


Pay Rate: $120.00 – $150.00 per hour (W2)
Location: Remote (Client HQ: Gainesville, FL – No relocation required)

Job Summary

We are seeking an experienced Biocompatibility Scientist to lead, plan, and execute biological safety evaluations for medical devices in alignment with the ISO 10993 series. This role supports product safety across the entire product lifecycle—new product development, sustaining engineering, and supplier/material change initiatives.

The ideal candidate has strong expertise in biocompatibility test strategies, chemical characterization, toxicological risk assessment, and regulatory compliance for medical devices.

Key Responsibilities

  • Develop and implement biocompatibility evaluation strategies for new products, product updates, and material changes.

  • Manage and oversee multiple biocompatibility projects simultaneously, ensuring timely completion and escalation of risks when needed.

  • Lead biological safety assessments per ISO 10993 standards, providing scientific justification and objective evidence supporting product safety.

  • Partner with cross-functional teams—including Regulatory Affairs, Clinical Affairs, R&D, QA, and Manufacturing Engineering—to ensure compliance and support project timelines.

  • Facilitate and coordinate laboratory activities such as:

    • Chemical characterization

    • Toxicological risk assessments

    • Biological testing

    • Lab investigations

  • Review, interpret, and summarize complex data into Biological Evaluation Plans (BEP) and Biological Evaluation Reports (BER).

  • Serve as a Subject Matter Expert (SME) for biocompatibility during regulatory submissions and interactions with FDA, BSI, and other competent authorities.

  • Ensure compliance with applicable Quality Systems, FDA regulations, and international biological safety standards.

Required Qualifications

  • Bachelor’s, Master’s, or Ph.D. in Biology, Biomedical Engineering, Toxicology, Materials Science, or related field.

  • Strong experience with ISO 10993 standards and biocompatibility assessments for medical devices.

  • Proven ability to interpret scientific data, drive testing strategies, and prepare compliant documentation.

  • Experience collaborating with regulatory bodies and supporting regulatory submissions.

  • Excellent communication, scientific writing, and project management skills.

Preferred Qualifications

  • Experience in orthopedic, implantable, or Class II/III medical devices.

  • Background in toxicological risk assessments and chemical characterization techniques.

  • Prior SME experience supporting audits or regulatory reviews.