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Biocompatibility Manager Jobs (NOW HIRING)

Biocompatibility Scientist

FL · Remote

$145 - $150/hr

Manage and oversee multiple biocompatibility projects simultaneously, ensuring timely completion and escalation of risks when needed. * Lead biological safety assessments per ISO 10993 standards ...

Actively involved in the planning, execution and management of experimental studies for the safety and efficacy characterization of new and existing products. * Serve as dedicated biocompatibility ...

• 2+ years of project management in a corporate setting • Experience managing multiple complex ... Biocompatibility review

... Management System ISO 13485:2016, ISO 10993 Biocompatibility are a significant benefit. The ideal candidate will be able to think critically, identify study risks before execution, recognize ...

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Biocompatibility Manager information

What are the key skills and qualifications needed to thrive as a Biocompatibility Manager, and why are they important?

To thrive as a Biocompatibility Manager, you need expertise in toxicology, materials science, and regulatory standards, typically supported by a degree in a life science field and experience with medical device biocompatibility testing. Familiarity with ISO 10993 standards, risk assessment tools, and regulatory submission systems is essential. Strong analytical thinking, attention to detail, and effective communication skills help in collaborating with cross-functional teams and ensuring regulatory compliance. These skills and qualities are vital for ensuring product safety, regulatory approval, and successful market entry for medical devices.

What are the common challenges a Biocompatibility Manager faces when coordinating cross-functional teams during product development?

A Biocompatibility Manager often encounters challenges in aligning the priorities and timelines of various teams such as R&D, regulatory affairs, and quality assurance. Ensuring clear communication about testing requirements and regulatory updates is vital, as misunderstandings can lead to delays or non-compliance issues. Additionally, the manager must balance thorough risk assessments with project deadlines, all while staying current with evolving international standards. Effective collaboration and proactive problem-solving are key to overcoming these challenges and ensuring the safety and compliance of medical devices.

What does a Biocompatibility Manager do?

A Biocompatibility Manager oversees the evaluation and testing of medical devices and materials to ensure they are safe and compatible with human tissues. Their responsibilities include designing testing protocols, interpreting regulatory requirements, and ensuring compliance with international standards like ISO 10993. They work closely with research, development, and regulatory teams to address any risks related to biological safety. Their work is critical for gaining regulatory approvals and ensuring patient safety.

What is the difference between Biocompatibility Manager vs Biocompatibility Specialist?

AspectBiocompatibility ManagerBiocompatibility Specialist
CredentialsTypically requires a degree in life sciences or biomedical engineering; certifications like ISO 10993 are commonSimilar educational background; often holds certifications in biocompatibility testing
Work EnvironmentOversees teams, manages projects, and ensures compliance across departmentsPerforms testing, data analysis, and reports within labs or R&D settings
Industry UsageUsed in regulatory, quality assurance, and management roles within medical device companiesPrimarily 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.

More about Biocompatibility Manager jobs
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What are the most commonly searched types of Biocompatibility jobs? The most popular types of Biocompatibility jobs are:
What states have the most Biocompatibility Manager jobs? States with the most job openings for Biocompatibility Manager jobs include:
Biocompatibility Program Manager

Biocompatibility Program Manager

Marmon

Hillsboro, OR

Full-time

Posted 5 days ago


Marmon Holdings rating

7.7

Company rating: 7.7 out of 10

Based on 13 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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