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Biocompatibility Manager Jobs in Massachusetts (NOW HIRING)

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 ...

Responsibilities The Regulatory Affairs Manager will report to the VP of Regulatory Affairs and ... Familiar with biocompatibility, sterilization, packaging, shelf life and associated ISO standards.

CNC Programmer

Lexington, MA · On-site

$70 - $100/hr

Manage material inventory, tooling, and consumables for the R&D machine shop. * Ensure ... Understanding ofmaterials and design considerations for biocompatibility, sterilization, and ...

Responsibilities The Regulatory Affairs Manager will report to the VP of Regulatory Affairs and ... Familiar with biocompatibility, sterilization, packaging, shelf life and associated ISO standards.

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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.

What are the most commonly searched types of Biocompatibility jobs in Massachusetts?

The most popular types of Biocompatibility jobs in Massachusetts are:

What are popular job titles related to Biocompatibility Manager jobs in Massachusetts?

For Biocompatibility Manager jobs in Massachusetts, the most frequently searched job titles are:

What job categories do people searching Biocompatibility Manager jobs in Massachusetts look for?

The top searched job categories for Biocompatibility Manager jobs in Massachusetts are:

What cities in Massachusetts are hiring for Biocompatibility Manager jobs?

Cities in Massachusetts with the most Biocompatibility Manager job openings:

Infographic showing various Biocompatibility Manager job openings in Massachusetts as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.

Manager, Global Toxicology and Biocompatibility

Boston Scientific

Marlborough, MA • Hybrid

Full-time

Posted 19 days ago


Boston Scientific rating

8.5

Company rating: 8.5 out of 10

Based on 120 frontline employees who took The Breakroom Quiz

32nd of 545 rated manufacturers


Job description

Additional Location(s): US-MA-Marlborough; US-MN-Arden Hills

Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance

At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we'll help you in advancing your skills and career. Here, you'll be supported in progressing - whatever your ambitions.           

 

About the role:

Global Toxicology and Biocompatibility plays a critical role in medical device development at Boston Scientific, ensuring patient safety while enabling early product development decisions, supporting product design direction, enabling product approvals, and supporting market launch for product commercialization. 

The Manager, Global Toxicology and Biocompatibility, provides technical leadership and support for the development of robust toxicology and biocompatibility processes to meet global business objectives. As the Manager, this position is responsible for ensuring processes and staff support the overall biological evaluation of medical device products. This includes support for new product development and sustaining activities, as well as global regulatory submissions, including related technical support to staff and project teams to meet business objectives.  This role will interface with internal stakeholders to plan, resource, and execute biocompatibility deliverables to support divisional and operational priorities.

Boston Scientific was recognized as a Glassdoor Best Place to Work in 2026, ranking No. 15 on the Top 100 list, reflecting the culture our employees experience every day.

At Boston Scientific, we value collaboration and synergy. This role follows a hybrid work model, requiring employees to be in our local office at least three (3) days per week.

Relocation assistance is not available for this position at this time.

Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time.

Your responsibilities will include:

  • Provide strategic leadership and guidance on the Global Toxicology and Biocompatibility process
  • Assist the Associate Director in setting Global Toxicology and Biocompatibility business objectives, influencing procedures, techniques, concepts, and approaches used at divisional levels for biocompatibility and toxicology programs
  • Serve as a key resource for biocompatibility and toxicology expertise for medical devices and pharmaceutical products for the Global Toxicology and Biocompatibility organization and assigned business divisions
  • Supervise scientific staff responsible for coordinating recommended biocompatibility testing with external research labs and assessing applicable test data
  • Provide strategic guidance and interpretation of regulatory requirements related to medical device submissions for the global organization and assigned business divisions
  • Develop close working relationships with R&D, regulatory affairs, quality engineering, and manufacturing, maintaining close communications with internal customers on biocompatibility and toxicology related deliverables
  • Ensure biocompatibility and toxicology information and data is accurate, reliable, and supports business objectives
  • May develop testing strategies, coordinate and monitor testing with external research labs, assess data, and author/review Biocompatibility Assessments and Reports for assigned business divisions
  • Act as a key liaison to external Contract Research Organizations for biocompatibility and toxicology testing
  • At the basis of every decision, demonstrate a primary commitment to patient safety and product quality

 

Required qualifications:

 

  • Bachelor's degree in chemistry, biochemistry, biology, biomedical engineering, toxicology, or a related field
  • Minimum of 8 years of professional toxicology/biocompatibility experience, or minimum of 6 years of professional toxicology/biocompatibility experience with an advanced degree
  • Minimum of 2 years of professional experience as a leader of technical people (not necessarily by means of direct reports)
  • Complete understanding and wide application of principles, theories, and concepts in the biocompatibility of medical devices, including demonstrated expertise with ISO 10993
  • Excellent written and verbal communication skills
  • Experience working with regulatory authorities

Preferred qualifications:

  • Advanced degree in chemistry, biochemistry, biology, biomedical engineering, toxicology, or a related field
  • Prior experience in medical device and/or pharmaceuticals
  • Comfortable in a dynamic environment and able to work independently as well as on teams
  • Results-oriented and detail-oriented, able to multi-task while working within aggressive timelines
  • Proven leadership and management of a technical group, providing coaching and development
  • Applied knowledge and understanding of toxicology principles and best practices
  • Working knowledge of quantitative toxicological risk assessment methodologies

Requisition ID: 632935 

Minimum Salary: $ 106800 

Maximum Salary: $ 202900 

The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) - see www.bscbenefitsconnect.com-will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, among other relevant business or organizational needs. At BSC, it is not typical for an individual to be hired near the bottom or top of the anticipated salary range listed above.

Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).

Compensation for exempt, non-sales roles may also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).

For MA positions: It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.

Boston Scientific transforms lives through innovative medical technologies that improve the health of patients around the world. As a global medical technology leader for more than 45 years, we advance science for life by providing a broad range of high-performance solutions that address unmet patient needs and reduce the cost of healthcare. Our portfolio of devices and therapies helps physicians diagnose and treat complex cardiovascular, respiratory, digestive, oncological, neurological and urological diseases and conditions. Learn more atwww.bostonscientific.comand follow us onLinkedIn.

Boston Scientific Corporation has been and will continue to be an equal opportunity employer. To ensure full implementation of its equal employment policy, the Company will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class.

Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status.  Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment.  Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements.   As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company's policies or protocols change with regard to COVID-19 vaccination.

Among other requirements, Boston Scientific maintains specific prohibited substance test requirements for safety-sensitive positions.  This role is deemed safety-sensitive and, as such, candidates will be subject to a prohibited substance test as a requirement.  The goal of the prohibited substance testing is to increase workplace safety in compliance with the applicable law.  


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About Boston Scientific

Sourced by ZipRecruiter

As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen.

Industry

Medical equipment and supplies manufacturing, manufacturing and construction

Company size

10,000+ Employees

Headquarters location

Marlborough, MA, US

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