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Contract Biocompatibility Scientist Jobs (NOW HIRING)

$120 - $170/hr

Manage biocompatibility testing programs with contract testing laboratories, ensuring GLP compliance and scientifically sound study design * Apply risk-based approaches to minimize redundant testing ...

Manage biocompatibility testing programs with contract testing laboratories, ensuring GLP compliance and scientifically sound study design * Apply risk-based approaches to minimize redundant testing ...

Research Scientist

Jacksonville, FL · On-site

$120 - $155/hr

Hybrid Contract Type: C2C Schedule: Monday-Friday, 8:00 AM-5:00 PM, with flexibility available Key ... including biocompatibility testing per ISO 10993 * Develop, review, and approve scientific ...

Research Scientist

Jacksonville, FL · On-site

$120 - $180/hr

Hybrid Contract Type: C2C Schedule: Monday-Friday, 8:00 AM-5:00 PM, with flexibility available Key ... including biocompatibility testing per ISO 10993 * Develop, review, and approve scientific ...

... sterility, biocompatibility, functionality, integrity and shelf life * Designs methods and ... A bachelor's degree in science, engineering, or other related technical discipline or equivalent ...

... or biocompatibility experience OR Advanced Degree in Science or technical field with 3+ years of ... Demonstrated understanding of the industrial sterilization business and contract sterilizer ...

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Contract Biocompatibility Scientist information

What is the difference between Contract Biocompatibility Scientist vs Contract Toxicologist?

AspectContract Biocompatibility ScientistContract Toxicologist
CredentialsBachelor's or Master's in Life Sciences, relevant certificationsBachelor's or Master's in Toxicology, related certifications
Work EnvironmentLaboratories, medical device companies, contract research organizationsLaboratories, pharmaceutical and biotech firms, regulatory agencies
Industry UsageMedical devices, implants, biomaterialsPharmaceuticals, chemicals, environmental safety

Contract Biocompatibility Scientists focus on evaluating the safety of medical devices and biomaterials for human use, ensuring they meet biocompatibility standards. Contract Toxicologists primarily assess chemical and drug safety, analyzing toxic effects and regulatory compliance. While both roles require scientific expertise and work in similar environments, their specific focus areas differ, making them distinct career paths within the broader field of safety assessment.

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Infographic showing various Contract Biocompatibility Scientist job openings in the United States as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 91% Full Time, 4% Part Time, and 3% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution.

Senior Biocompatibility Scientist

Physiol

On-site

$120 - $170/hr

Other

Posted 4 days ago


Job description

  • Conduct retrospective biocompatibility gap assessments across legacy product families, generating or compiling documentation to establish a comprehensive baseline of biological safety evidence
  • Support sustaining and change management activities by providing strategic assessment of biological safety impact in accordance with ISO 10993-1
  • Develop and execute biocompatibility evaluation plans (BEPs) for new product development initiatives in accordance with ISO 10993-1 and FDA guidance, aligned to device classification, contact type, and contact duration
  • Author and review biological evaluation reports (BERs), toxicological risk assessments (TRAs), and material characterization reports supporting 510(k), PMA, De Novo, and international submissions (CE marking under MDR, etc.)
  • Manage biocompatibility testing programs with contract testing laboratories, ensuring GLP compliance and scientifically sound study design
  • Apply risk-based approaches to minimize redundant testing, leveraging existing data where scientifically justified
  • Support post-market and complaint driven biological safety assessments
  • Serve as biocompatibility subject matter expert during FDA/notified body interactions, audits, and responses to regulatory questions or deficiency letters
  • Develop and maintain SOPs, templates, and standardized workflows for biocompatibility evaluations to improve consistency, efficiency, and audit-readiness across the organization
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