Marmon

Biocompatibility Program Manager

United States · Work style not stated · Full time

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About the role

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EmployerMarmon
LocationUnited States
Work styleWork style not stated
Employment typeFull time
Employer posted24 Apr 2026

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 ScopeTheBiocompatibility 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.

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Duties/Responsibilities

Works independently and on cross-functional teams in 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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