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Biocompatibility Remote Jobs (NOW HIRING)

Managed Staffing

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 ...

Kelly Services

Biocompatibility Coordinator

Blue Ash, OH · On-site +1

$37/hr

Biocompatibility Coordinator Blue Ash, Ohio Mon - Fri 8am-5pm (Hybrid) 3 days on site/2 days remote Hourly Rate: $37/hr W2 Long-term engagement at one of our Global medical device clients. The role ...

Pace

Chemical Regulatory Coordinator (Remote)

Eagan, MN · On-site +1

$21 - $23/hr

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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Biocompatibility Remote information

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

To thrive as a Biocompatibility Specialist, you need a solid background in biological sciences, toxicology, or biomedical engineering, often supported by a relevant degree and experience with medical device regulations. Familiarity with ISO 10993 standards, risk assessment tools, and regulatory submission systems is typically required. Strong analytical thinking, attention to detail, and effective written communication are essential soft skills, especially in a remote environment. These competencies ensure accurate safety evaluations and successful regulatory approvals for medical devices, even when collaborating virtually.

What are some common challenges faced by remote biocompatibility professionals, and how can they be effectively managed?

Remote biocompatibility professionals often encounter challenges related to cross-functional communication and access to laboratory data, as much of the work involves collaborating with regulatory, R&D, and laboratory teams. To manage these challenges, it is important to establish clear communication channels, schedule regular virtual meetings, and utilize collaborative project management tools. Staying organized and proactively reaching out to on-site team members for data clarification can also help ensure projects remain on track and meet regulatory deadlines.

What are Biocompatibility Remote jobs?

Biocompatibility Remote jobs involve assessing and ensuring that medical devices, materials, or products are safe and compatible with biological systems while working from a remote location. Professionals in these roles typically conduct risk assessments, review scientific literature, and prepare regulatory documentation to support biocompatibility claims. They collaborate with cross-functional teams, interpret regulatory standards such as ISO 10993, and help guide product development to meet safety requirements. Remote biocompatibility specialists leverage digital tools to communicate and manage projects effectively from outside a traditional office setting.

What is the difference between Biocompatibility Remote vs Biocompatibility Specialist?

AspectBiocompatibility RemoteBiocompatibility Specialist
CredentialsTypically requires knowledge of biocompatibility testing, certifications varyRequires certifications like ISO 10993, relevant degrees, and experience
Work EnvironmentPrimarily remote, involving documentation, research, and communicationOften lab-based or on-site testing, but may include remote report review
Employer & Industry UsageUsed by medical device companies, contract labs, and regulatory consultantsEmployed by medical device manufacturers, testing labs, and regulatory agencies

While both roles focus on biocompatibility, Biocompatibility Remote typically involves remote research, documentation, and compliance tasks, whereas a Biocompatibility Specialist often conducts hands-on testing and lab work. The remote role offers flexibility, while the specialist role emphasizes direct testing expertise.

More about Biocompatibility Remote jobs
What cities are hiring for Biocompatibility Remote jobs? Cities with the most Biocompatibility Remote job openings:
What are the most commonly searched types of Biocompatibility jobs? The most popular types of Biocompatibility jobs are:
What states have the most Biocompatibility Remote jobs? States with the most job openings for Biocompatibility Remote jobs include:
What job categories do people searching Biocompatibility Remote jobs look for? The top searched job categories for Biocompatibility Remote jobs are:
Biocompatibility Remote jobs near you
Infographic showing various Biocompatibility Remote job openings in the United States as of May 2026, with employment types broken down into 76% Part Time, and 24% Contract. Highlights an 100% Remote job distribution.
Biocompatibility Scientist

Biocompatibility Scientist

Managed Staffing

Remote

$145 - $150/hr

Contractor

Posted 26 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.