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Biocompatibility Manager Jobs (NOW HIRING)

Managed Staffing

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 ...

Abbott

Director, Biocompatibility

Saint Paul, MN · On-site

Team & Functional Management: * Lead and mentor teams of biocompatibility scientists across multiple sites. * Foster a culture of collaboration, accountability, and continuous improvement. * Oversee ...

Physiol

$120 - $170/hr

Support sustaining and change management activities by providing strategic assessment of biological safety impact in accordance with ISO 10993-1 * Develop and execute biocompatibility evaluation ...

Abbott

Director, Biocompatibility

Santa Clara, CA · On-site

Team & Functional Management: * Lead and mentor teams of biocompatibility scientists across multiple sites. * Foster a culture of collaboration, accountability, and continuous improvement. * Oversee ...

Physiol

Senior Biocompatibility Scientist

Waltham, MA · On-site

$120 - $170/hr

Support sustaining and change management activities by providing strategic assessment of biological safety impact in accordance with ISO 10993-1 * Develop and execute biocompatibility evaluation ...

Abbott

Director, Biocompatibility

Santa Clara, CA · On-site

Team & Functional Management: * Lead and mentor teams of biocompatibility scientists across multiple sites. * Foster a culture of collaboration, accountability, and continuous improvement. * Oversee ...

Abbott

Senior Biocompatibility Scientist II

Santa Clara, CA · On-site

$107K - $146K/yr

This role is a senior individual contributor position and does not include direct people management responsibilities. Responsibilities: * Conduct and document biocompatibility assessments, develop ...

Abbott

Senior Biocompatibility Scientist II

Saint Paul, MN · On-site

$92K - $126K/yr

This role is a senior individual contributor position and does not include direct people management responsibilities. Responsibilities: * Conduct and document biocompatibility assessments, develop ...

Abbott

Senior Biocompatibility Scientist II

Santa Clara, CA · On-site

$107K - $146K/yr

This role is a senior individual contributor position and does not include direct people management responsibilities. Responsibilities: * Conduct and document biocompatibility assessments, develop ...

Abbott Laboratories

$100 - $200/hr

This role is a senior individual contributor position and does not include direct people management responsibilities.**Responsibilities:*** Conduct and document biocompatibility assessments, develop ...

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Biocompatibility Manager information

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

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 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.

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Biocompatibility Manager jobs near you
Infographic showing various Biocompatibility Manager job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 92% In-person, and 8% Hybrid job distribution.

Biocompatibility Program Manager

Marmon Holdings, Inc.

Hillsboro, OR • On-site

$90 - $120/hr

Other

Re-posted 8 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

**Job Scope** The Biocompatibility Program Manager is responsible for establishing and directing all aspects of the biocompatibility (“biocomp”) program for Acumed (“the Company”).. This individual will ensure all products released and in the field are in compliance with current biocompatibility standards for safe use of products in patients. This individual will work cross functionally with each business unit to ensure biocomp principles are appropriately applied to new product development. This individual will ensure the organization understands the importance of biocomp principles and procedures, provide appropriate training, guidance, and will review and approve final biocomp documentation. This individual will manage and report on the status of biocomp initiatives to management teams, including the executive team on a periodic basis. This individual will work within a matrixed organization, and may directly manage others on the biocompatibility team.Authors, reviews and approves biocomp evaluation plans, test reports, and final biocompatibility reports.Uses project management tools to manage biocompatibility program initiatives. current with biocompatibility standards, knowledge of Understands and utilizes Acumed project funding processes to manages all aspects of biocompatibility budget (planning process, budget levels and spend, etc.) Supports new product development across all business units for biocompatibility compliance. - Completes the duties described in the Quality Manual.- Preferred: advanced education in toxicology or microbiologyMinimum 5 years of experience applying biocompatibility (surgically invasive and implantable) principles.Proficiency in Project Management for organizing and managing deliverables.Ability to multitask and prioritize projects that align with departmental and organizational objectives.- Strong technical writing, verbal, and interpersonal communication skillsProficiency of testing methods (bioburden, Cytotoxicity, Irritation, Extractible/Leachable, Sensitization, etc.)Working knowledge of statistical models and how to apply to test data for biological evaluations.Proficiency with ISO-10993, ISO-14971, FDA and EU-MDR regulations and application to biocompatibility evaluations.- Familiarity to SAP, Windchill, CAD softwareWherever you're at in your career, our people and resources will help you go further. As you grow your skills, you can also move up and around our 120+ companies. #J-18808-Ljbffr

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