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Remote Biocompatibility Scientist Jobs (NOW HIRING)

Biocompatibility Scientist

FL · Remote

$145 - $150/hr

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 ...

Biocompatibility Coordinator At Kelly ® Science, Engineering, Technology & Telecom (SETT), we're ... Biocompatibility Coordinator Blue Ash, Ohio Mon - Fri 8am-5pm (Hybrid) 3 days on site/2 days remote ...

Biocompatibility Coordinator At Kelly ® Science, Engineering, Technology & Telecom (SETT), we're ... Biocompatibility Coordinator Blue Ash, Ohio Mon - Fri 8am-5pm (Hybrid) 3 days on site/2 days remote ...

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

Compile and summarize biocompatibility test data and study results * Perform qualitative toxicology assessments using existing data, regulatory classifications, and scientific literature * Gap ...

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Remote Biocompatibility Scientist information

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$83.5K

$127K

$171K

How much do remote biocompatibility scientist jobs pay per year?

As of Jun 9, 2026, the average yearly pay for remote biocompatibility scientist in the United States is $127,031.00, according to ZipRecruiter salary data. Most workers in this role earn between $109,000.00 and $143,500.00 per year, depending on experience, location, and employer.

What is the difference between Remote Biocompatibility Scientist vs Remote Regulatory Affairs Specialist?

AspectRemote Biocompatibility ScientistRemote Regulatory Affairs Specialist
Required CredentialsDegree in life sciences, certification in biocompatibility testingDegree in life sciences or law, regulatory certifications (e.g., RAC)
Work EnvironmentLaboratories, research settings, medical device companiesRegulatory agencies, medical device or pharmaceutical companies
Industry UsageMedical devices, implants, biomaterialsMedical devices, pharmaceuticals, healthcare products
Common Search/ComparisonYesYes

The Remote Biocompatibility Scientist focuses on testing and evaluating the safety of medical materials and devices, ensuring they are biocompatible. In contrast, the Remote Regulatory Affairs Specialist manages regulatory submissions and compliance for medical products. While both roles require knowledge of industry standards, their core responsibilities and work environments differ significantly.

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

To thrive as a Remote Biocompatibility Scientist, you need a strong background in biomedical sciences, toxicology, or materials science, usually supported by a relevant degree and experience with ISO 10993 standards. Familiarity with laboratory information management systems (LIMS), biocompatibility testing methods, and regulatory documentation tools is typically required. Excellent analytical thinking, attention to detail, and effective written communication are vital soft skills for collaborating remotely and preparing clear reports. These skills ensure accurate biocompatibility assessments, regulatory compliance, and smooth teamwork in a remote work environment.

How does a Remote Biocompatibility Scientist typically collaborate with cross-functional teams in a virtual environment?

As a Remote Biocompatibility Scientist, you will frequently collaborate with regulatory, engineering, and quality assurance teams through virtual meetings and collaborative platforms. Effective communication is key, as you’ll need to interpret biocompatibility data, provide guidance on regulatory submissions, and align testing strategies with product development goals. Most companies use project management tools and regular video conferences to ensure smooth coordination and timely updates. Building clear documentation and maintaining proactive communication help overcome the challenges of remote work and ensure successful team outcomes.

What is a Remote Biocompatibility Scientist?

A Remote Biocompatibility Scientist is a professional who evaluates the compatibility of medical devices and materials with biological systems, such as human tissues, while working remotely. They are responsible for assessing the safety of materials used in medical devices to ensure they don't cause adverse reactions when in contact with the body. Their work involves reviewing scientific data, conducting risk assessments, and preparing documentation for regulatory submissions, often collaborating with interdisciplinary teams from a remote location. This role requires expertise in toxicology, biology, and regulatory standards such as ISO 10993.
More about Remote Biocompatibility Scientist jobs
What cities are hiring for Remote Biocompatibility Scientist jobs? Cities with the most Remote Biocompatibility Scientist job openings:
What are the most commonly searched types of Biocompatibility Scientist jobs? The most popular types of Biocompatibility Scientist jobs are:
What states have the most Remote Biocompatibility Scientist jobs? States with the most job openings for Remote Biocompatibility Scientist jobs include:
Infographic showing various Remote Biocompatibility Scientist job openings in the United States as of May 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution, with an average salary of $127,031 per year, or $61.1 per hour.
Biocompatibility Scientist

Biocompatibility Scientist

Managed Staffing

FL • Remote

$145 - $150/hr

Contractor

Posted 5 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.