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Biocompatibility Scientist Jobs (NOW HIRING)

Cellanome

Staff Scientist, Chemistry

Foster City, CA

$140K - $200K/yr

Cellanome is seeking an experienced chemist or materials scientist to advance the development and ... Experience with biocompatibility evaluation of biomaterials. The estimated base salary range for ...

Actalent

Product Development Engineer

Jacksonville, FL

$70K - $85K/yr

Job Title: product development specialist Join our team as a V&V Biocompatibility Specialist where ... Additional Skills & Qualifications * BS degree in scientific disciplines such as material science ...

New

Fortive

Senior Scientist, R&D Chemistry

Irvine, CA

$97K - $133K/yr

The Senior Scientist, R&D Chemistry, works under limited supervision and uses knowledge of ... biocompatibility. * Supports design changes for marketed products, such as manufacturing steps ...

Amgen

Senior Principal Scientist

Thousand Oaks, CA · On-site +1

Support device organization with expertise on biocompatibility evaluations (ISO 10993-1) and more ... Monitor scientific developments and conduct desktop research including literature searches and ...

Amgen SA

Senior Principal Scientist

Thousand Oaks, CA · On-site

$180 - $240/hr

Support device organization with expertise on biocompatibility evaluations (ISO 10993-1) and more ... Monitor scientific developments and conduct desktop research including literature searches and ...

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Biocompatibility Scientist information

What does a biocompatibility scientist do?

A Biocompatibility Scientist evaluates the compatibility of medical devices, biomaterials, and pharmaceuticals with biological systems to ensure safety and regulatory compliance. They conduct risk assessments, review toxicological data, and design biocompatibility testing strategies following international standards like ISO 10993. Their work involves collaborating with regulatory bodies, R&D teams, and quality assurance to ensure products meet health and safety requirements before market release.

What are the key skills and qualifications needed to thrive as a biocompatibility scientist?

To thrive as a Biocompatibility Scientist, you need a strong background in biology, chemistry, or biomedical engineering, typically supported by an advanced degree and experience with regulatory standards like ISO 10993. Expertise with laboratory analytical techniques (such as cytotoxicity, sensitization assays), data analysis software, and familiarity with submission processes for agencies like the FDA or EMA are highly valued. Strong attention to detail, effective communication, and collaboration skills are essential for working in multidisciplinary teams and documenting findings clearly. These competencies ensure the safety and compliance of medical devices or materials, which is critical for successful product development and regulatory approval.

What types of projects and collaborations are common for biocompatibility scientists in a typical work setting?

Biocompatibility Scientists often work on projects that evaluate the safety of medical devices, materials, or pharmaceuticals by designing and conducting biological tests. They regularly collaborate with R&D, regulatory affairs, quality assurance, and clinical research teams to interpret results and prepare documentation for regulatory submissions. Daily responsibilities may include running laboratory assays, analyzing data, writing technical reports, and presenting findings in cross-functional meetings. Close interaction with project managers and engineers is common to ensure testing aligns with product development timelines and compliance requirements. This multidisciplinary environment provides excellent opportunities to broaden expertise and advance into leadership or regulatory strategy roles.

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The top searched job categories for Biocompatibility Scientist jobs are:

Biocompatibility Scientist jobs near you
Infographic showing various Biocompatibility Scientist job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 81% In-person, 13% Hybrid, and 6% Remote job distribution.

Sr. Scientist, Toxicology (Board Certified) - Bracco Medical Technologies

Bracco

Eden Prairie, MN • On-site

$160K - $173K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 15 days ago

Job description

Why Join Bracco Medical Technologies?
We care as much about our employees as we do our patients. Our culture fosters a work environment where employees can thrive, be passionate and have fun along the way. Each member of the Bracco Medical Technologies team has the power to make a difference......every day!
The Sr. Scientist, Toxicologist will have responsible for providing leadership and support for biocompatibility and chemical characterization testing encompassing extractable and leachable analysis and evaluating the harmful effects of chemicals on Bracco Medical Technologies (BMT) products, determining the safe exposure levels, and ensuring compliance to BMT design control procedures and applicable regulations and external standards.
Primary Duties & Responsibilities:
  • Support biocompatibility and other chemical and toxicology testing for consumable devices to identify, understand, and assess the toxic effects of identified chemicals and substances on patients supported by BMT products.
  • Interpreting data from studies, drawing conclusions, and making recommendations for safety and regulatory compliance.
  • Advising on safe exposure levels for substances identified in BMT products.
  • Collaborating with project teams and testing facilities in the development of testing required for assessment of biocompatibility.
  • Providing expert advice in legal and regulatory matters related to toxicology.
  • Lead Biological Evaluation Plans (BEPs) and Biological Evaluation Reports (BERs) in accordance with ISO 10993.
  • Conduct toxicological risk assessments supporting product development, design changes, supplier changes, and regulatory submissions.
  • Provide technical leadership for extractables and leachables (E&L) studies, including protocol development, data review, and report approval.
  • Partner with R&D, Design Assurance, Regulatory Affairs, and Supplier Quality to integrate biological safety throughout the product lifecycle.
  • Monitor emerging regulatory requirements and maintain internal biological safety procedures, standards, and best practices.

Does this position have supervisory authority? Yes ☐ No ☒
Qualifications (Knowledge, Skills & Abilities):
Minimum
  • Bachelor's degree in Toxicology, Chemistry, Biology or other related technical / scientific background
  • 10+ years of experience in Toxicology or a related field.
  • Board certified toxicologist (DABT or equivalent) is required.
  • Working knowledge of the FDA Quality System Regulation and EU Medical Device Regulations.
  • Experience performing toxicological risk assessments and biological evaluations in accordance with ISO 10993 and ISO 14971.
  • Knowledge of extractables and leachables (E&L) studies, analytical chemistry techniques, and interpretation of analytical data.
  • Moderate level of computer proficiency including MS Word, Excel, Project, and statistical applications software.
  • Effective oral and written communication skills.
  • Effective technical writing skills.
  • Ability to work independently and prioritize assignments to meet project timelines.

Preferred:
  • Masters degree plus 7 years in Toxicology or a related field, or PhD in Toxicology plus 3 years of experience in Toxicology or a related field.
  • Demonstrated knowledge of ISO 10993 series of standards.
  • Experience authoring Biological Evaluation Plans (BEPs), Biological Evaluation Reports (BERs), and supporting FDA, MDR, and other global regulatory submissions.
  • Experience managing external testing laboratories and collaborating with cross-functional teams throughout the medical device product lifecycle.

Other:
  • Travel expected to be less than 10%.

Compensation & Total Rewards:
Estimated Starting Salary Range: $160,000 - 173,000
*Estimated salary is intended to reflect the salary Bracco Medical Technologies reasonably expects to pay for the position. The provided range is based on salary and market data and may vary based on an employee's eligibility for geographic differential pay in high-cost-of-labor markets.
Total Rewards:
  • Paid Time Off, Company Holidays & Paid Family Leave - We provide PTO and Company Holidays to help you recharge, relax and do what's important to you, when it's important to you. Our 100% paid family leave options for parents, grandparents and eligible family members provide support for growing families as well.
  • Achieve - Beyond competitive compensation, we offer options to help you plan for a financially secure future, including an annual incentive plan and 401k savings plan contributions.
  • Live well - We offer comprehensive benefit options to help protect you along the way, including medical, dental, vision, and life insurance, employer HSA contributions, employee assistance program, short-term disability, etc.
  • Evolve - Through structured on-the-job learning, workshops, seminars, and our tuition reimbursement program, you'll find many opportunities to grow, personally and professionally.
  • Choose -You won't find "stuffy" here whether your position requires a hybrid or in-the-office working arrangement. That means business casual for your attire and flexibility in your schedule, wherever possible.

Bracco Medical Technologies is an Affirmative Action/Equal Opportunity Employer. Bracco Medical Technologies desires priority referrals of protected veterans for all openings.

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