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Biocompatibility Scientist Jobs (NOW HIRING)

Bachelor's degree in biological or physical sciences, or engineering * Preferred: advanced education in toxicology or microbiology * Minimum 5years ofexperience applying biocompatibility (surgically ...

Job Summary This position serves as the polymer and biocompatibility material science subject matter expert for single-use systems, primary packaging, and polymeric components used across drug ...

Scientist I

Rochester, NY · On-site

$60 - $85/hr

Analytical Chemist position supporting the Surgical Analytical + Materials Science R+D function in ... Support biocompatibility and chemical characterization activities aligned with ISO 10993 ...

Analytical Chemist position supporting the Surgical Analytical + Materials Science R+D function in ... Support biocompatibility and chemical characterization activities aligned with ISO 10993 ...

... biocompatibility assessments, product improvement initiatives, complaint and root-cause ... scientists and project leads. • Analyze and interpret analytical data, identify trends or ...

Senior R&D Scientist, Biomaterials

West Chester, PA · On-site

$86K - $118K/yr

Scientific/Technology All Job Posting Locations: West Chester, Pennsylvania, United States of ... Design, plan, and execute laboratory studies to assess material properties, biocompatibility, and ...

Showing results 21-40

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:

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.

Biocompatibility Program Manager

Marmon

Hillsboro, OR • On-site

Full-time

Re-posted 14 days ago


Marmon Holdings rating

7.7

Company rating: 7.7 out of 10

Based on 15 frontline employees who took The Breakroom Quiz


Job description

Acumed LLC

As a part of the global industrial organization Marmon Holdings-which is backed by Berkshire Hathaway-you'll be doing things that matter, leading at every level, and winning a better way. We're committed to making a positive impact on the world, providing you with diverse learning and working opportunities, and fostering a culture where everyone's empowered to be their best.

Job Scope TheBiocompatibility Program Manageris responsible forestablishingand directing all aspects of the biocompatibility("biocomp")program forAcumed("theCompany").. This individual will ensure all products released and in the fieldare in compliance withcurrent biocompatibility standards for safe use of products inpatients. This individual will work cross functionally with each business unit to ensurebiocompprinciples are appropriately applied to new product development.This individual will ensuretheorganization understandstheimportance ofbiocompprinciples and procedures, provideappropriate training,guidance,andwillreview and approve finalbiocompdocumentation.This individual will manage and report onthestatus ofbiocompinitiatives to management teams, includingtheexecutive teamon a periodic basis. This individualwillwork within a matrixed organization, and may directly manage others on the biocompatibility team.

Duties/Responsibilities

  • Worksindependently andoncross-functionalteamsin a matrixed environment.
  • Communicatestechnical principles related tobiocompeffectivelyandinfluenceskey stakeholders internally and externally.
  • Authors, reviewsand approvesbiocompevaluation plans,test reports,andfinal biocompatibility reports.
  • Responsible for presentingbiocompprogram updatesto large audiences, includingthe Executive Team
  • Usesproject management tools to manage biocompatibility program initiatives.
  • Remainscurrent with biocompatibility standards,testingand regulatory interpretations inthemedical deviceindustry.
  • Createsand trainsothers onwork practices in compliance with applicable ISO and CFR regulations/guidance.
  • Appliesappropriate testingmethods forbiocompevaluations (i.e., cytotoxicity, sensitization, MMP, Irritation, Extractable / Leachable, etc.)
  • Applyappropriatestatisticalprinciples tobiocomptestingandanalysis.
  • Utilizesknowledge ofAcumedproducts andtheirindicationsand method of use to evaluate biological indicators andrisks.
  • Independently manages external vendorsand consultants (i.e.,toxicologist, test houses, etc.)
  • Understandsand utilizesAcumedproject funding processes tomanages all aspects of biocompatibility budget (planning process, budget levels and spend, etc.)
  • Participates as a member of technical review boards for applicable projects/expertise.
  • Interfacesand collaborates with department leaders to influence and helpshapeCompanystrategic initiativesrelated tobiocomp.
  • Supportsnew product development across all business units for biocompatibility compliance.
  • Work withinengineering systems, includingSAP, CAD, Windchillto perform job functions and document results.
  • Follows and works withinAcumed'sDesign Control process and framework.
  • Completes the duties described in the Quality Manual.

Qualifications

  • Bachelor's degree in biological or physical sciences, or engineering
  • Preferred: advanced education in toxicology or microbiology
  • Minimum 5years ofexperience applying biocompatibility (surgically invasive and implantable) principles.
  • Proficiencyin Project Management for organizing and managing deliverables.
  • Ability to multitask and prioritize projects that align with departmental and organizationalobjectives.
  • Strong technical writing, verbal, and interpersonal communication skills
  • Proficiencyof testing methods(bioburden, Cytotoxicity, Irritation, Extractible/Leachable, Sensitization, etc.)
  • Working knowledge of statistical modelsand how to apply to test data for biological evaluations.
  • Proficiencywith ISO-10993, ISO-14971, FDA and EU-MDR regulations and application to biocompatibility evaluations.
  • Familiarity to SAP, Windchill, CAD software

Following receipt of a conditional offer of employment, candidates will be required to complete additional job-related screening processes as permitted or required by applicable law.

We are an equal opportunity employer, and all applicants will be considered for employment without attention to their membership in any protected class. If you require any reasonable accommodation to complete your application or any part of the recruiting process, please email your request to careers@marmon.com, and please be sure to include the title and the location of the position for which you are applying.


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