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Biocompatibility Jobs 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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How much do biocompatibility jobs remote jobs pay per hour?

As of May 29, 2026, the average hourly pay for biocompatibility jobs remote in the United States is $19.97, according to ZipRecruiter salary data. Most workers in this role earn between $16.83 and $21.15 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in a remote biocompatibility role, and why are they important?

To thrive in a remote biocompatibility job, you need a solid background in life sciences, biomedical engineering, or a related field, often supported by experience with ISO 10993 standards and regulatory requirements. Familiarity with data analysis tools, report writing software, and document management systems like Veeva Vault or MasterControl is typically required. Attention to detail, strong written communication, and self-motivation are essential soft skills for remote collaboration and independent work. These competencies ensure high-quality, compliant assessments of medical device materials and effective teamwork across dispersed teams.

What are some common challenges faced by professionals in remote biocompatibility roles, and how can they be addressed?

Professionals working in remote biocompatibility roles often face challenges related to effective collaboration across multidisciplinary teams, as well as accessing physical laboratory resources. Clear communication with regulatory, engineering, and laboratory teams is vital to ensure project milestones are met. Utilizing digital project management tools, scheduling regular virtual meetings, and staying updated on regulatory changes can help overcome these obstacles. Additionally, remote biocompatibility specialists should proactively seek feedback and maintain detailed documentation to facilitate smooth teamwork and compliance.

What are biocompatibility jobs and can they be done remotely?

Biocompatibility jobs involve assessing and ensuring that materials and products, such as medical devices, are safe and compatible with biological systems. These roles often include tasks like reviewing scientific literature, writing reports, designing test protocols, and interpreting laboratory results. With advancements in digital tools and secure communication platforms, many biocompatibility jobs can now be performed remotely, especially those focused on documentation, regulatory submissions, and consultation. However, some positions may still require occasional onsite work for hands-on testing or lab coordination.

What is the difference between Biocompatibility Jobs Remote vs Medical Device Quality Assurance Jobs Remote?

AspectBiocompatibility Jobs RemoteMedical Device Quality Assurance Jobs Remote
Required CredentialsBiocompatibility certifications, life sciences degreesQuality assurance certifications, engineering or life sciences degrees
Work EnvironmentRemote, primarily research and testing documentationRemote, audits, documentation review, compliance tasks
Industry UsageMedical device manufacturing, biomaterialsMedical device manufacturing, regulatory compliance
Common Search/ComparisonYesYes

Biocompatibility Jobs Remote and Medical Device Quality Assurance Jobs Remote both involve working in the medical device industry with a focus on compliance and safety. While biocompatibility roles emphasize testing and certification of materials, quality assurance roles focus on ensuring overall product compliance and regulatory adherence. Both positions often require similar certifications and can be performed remotely, making them comparable career paths within the medical device sector.

Biocompatibility Scientist

Biocompatibility Scientist

Managed Staffing

Remote

$145 - $150/hr

Contractor

Posted 25 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.