Usesproject management tools to manage biocompatibility program initiatives. * Remainscurrent with biocompatibility standards,testingand regulatory interpretations inthemedical deviceindustry.
Usesproject management tools to manage biocompatibility program initiatives. * Remainscurrent with biocompatibility standards,testingand regulatory interpretations inthemedical deviceindustry.
Manager of Microbiology & Sterility
$140K - $170K/yr
Oversee Microbiological/Biocompatibility efforts in support of NPD/Sustaining Engineering efforts ... Strong project management skills with the ability to prioritize for maximum results (multi-task ...
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Manager of Microbiology & Sterility
$140K - $170K/yr
Oversee Microbiological/Biocompatibility efforts in support of NPD/Sustaining Engineering efforts ... Strong project management skills with the ability to prioritize for maximum results (multi-task ...
Manager of Microbiology & Sterility
$140K - $170K/yr
Oversee Microbiological/Biocompatibility efforts in support of NPD/Sustaining Engineering efforts ... Strong project management skills with the ability to prioritize for maximum results (multi-task ...
Manager of Microbiology & Sterility
$140K - $170K/yr
Oversee Microbiological/Biocompatibility efforts in support of NPD/Sustaining Engineering efforts ... Strong project management skills with the ability to prioritize for maximum results (multi-task ...
The Biocompatibility Team is responsible for executing a wide range of assays, performing method ... management, and other general laboratory tasks. The primary goal of the Chemist is to support ...
The Biocompatibility Team is responsible for executing a wide range of assays, performing method ... management, and other general laboratory tasks. The primary goal of the Chemist is to support ...
Chemist
Austin, TX · On-site
$71K - $119K/yr
The Biocompatibility Team is responsible for executing a wide range of assays, performing method ... management, and other general laboratory tasks. The primary goal of the Chemist is to support ...
Chemist
Austin, TX · On-site
$71K - $119K/yr
The Biocompatibility Team is responsible for executing a wide range of assays, performing method ... management, and other general laboratory tasks. The primary goal of the Chemist is to support ...
Manages the personnel activities of the Regulatory Affairs and Document Control departments ... Provides oversight of third party testing (UL, EMC, biocompatibility, sterilization assurance) as ...
Manages the personnel activities of the Regulatory Affairs and Document Control departments ... Provides oversight of third party testing (UL, EMC, biocompatibility, sterilization assurance) as ...
Manages the personnel activities of the Regulatory Affairs and Document Control departments ... Provides oversight of third party testing (UL, EMC, biocompatibility, sterilization assurance) as ...
Manages the personnel activities of the Regulatory Affairs and Document Control departments ... Provides oversight of third party testing (UL, EMC, biocompatibility, sterilization assurance) as ...
Contribute to cross-functional problem-solving on topics ranging from biocompatibility and ... Hands-on background in medical device design, testing, risk management (ISO 14971), or preclinical ...
Contribute to cross-functional problem-solving on topics ranging from biocompatibility and ... Hands-on background in medical device design, testing, risk management (ISO 14971), or preclinical ...
Regulatory Engineer
Austin, TX · On-site
$71K - $119K/yr
Contribute to cross-functional problem-solving on topics ranging from biocompatibility and ... Hands-on background in medical device design, testing, risk management (ISO 14971), or preclinical ...
Regulatory Engineer
Austin, TX · On-site
$71K - $119K/yr
Contribute to cross-functional problem-solving on topics ranging from biocompatibility and ... Hands-on background in medical device design, testing, risk management (ISO 14971), or preclinical ...
Microbiologist
Austin, TX · On-site
Head of Biocompatibility and Sterility Location: Austin, TX Business Unit Description: Quality ... Manages dose audit program and annual sterilizer requalification * Support product development for ...
Microbiologist
Austin, TX · On-site
Head of Biocompatibility and Sterility Location: Austin, TX Business Unit Description: Quality ... Manages dose audit program and annual sterilizer requalification * Support product development for ...
Head of Biocompatibility and Sterility Location: Austin, TX Business Unit Description: Quality ... Manages dose audit program and annual sterilizer requalification * Support product development for ...
Head of Biocompatibility and Sterility Location: Austin, TX Business Unit Description: Quality ... Manages dose audit program and annual sterilizer requalification * Support product development for ...
Biocompatibility Manager information
What are the key skills and qualifications needed to thrive as a Biocompatibility Manager, and why are they important?
What are the common challenges a Biocompatibility Manager faces when coordinating cross-functional teams during product development?
What does a Biocompatibility Manager do?
What is the difference between Biocompatibility Manager vs Biocompatibility Specialist?
| Aspect | Biocompatibility Manager | Biocompatibility Specialist |
|---|---|---|
| Credentials | Typically requires a degree in life sciences or biomedical engineering; certifications like ISO 10993 are common | Similar educational background; often holds certifications in biocompatibility testing |
| Work Environment | Oversees teams, manages projects, and ensures compliance across departments | Performs testing, data analysis, and reports within labs or R&D settings |
| Industry Usage | Used in regulatory, quality assurance, and management roles within medical device companies | Primarily involved in testing and technical analysis within laboratories |
The main difference is that the Biocompatibility Manager oversees testing programs and compliance strategies, while the Biocompatibility Specialist focuses on conducting tests and technical analysis. Both roles require similar credentials but differ in scope and responsibilities.

Marmon Holdings rating
7.7
Based on 15 frontline employees who took The Breakroom Quiz
Job description
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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