Biocompatibility scientist

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at

Job Function:

R&D Product Development

Job Sub Function:

Materials/Biomaterials Science

Job Category:

Scientific/Technology

All Job Posting Locations:

Danvers, Massachusetts, United States of America, Houston, Texas, United States of America

Job Description:

About MedTech

Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.

Your unique talents will help patients on their journey to wellness. Learn more at

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at .

This is a remote role available in Danvers/Houston within the US. While specific cities are listed in the Locations section for reference, please note that they are examples only and do not limit your application. We invite candidates from any location to apply.

#LI-Remote

An internal pre-identified candidate for consideration has been identified. However, all applications will be considered.

We are searching for the best talent for Biocompatibility Scientist to be in Danvers, MA .

Position Overview

We are seeking a Biocompatibility and Toxicology Subject Matter Expert (SME) to join our team. This role involves leading complex biocompatibility and toxicology projects, providing expert scientific assessments, and ensuring compliance with international standards such as ISO 10993. The ideal candidate will serve as a key technical resource across functions. This position offers an opportunity to influence product safety, regulatory strategy, and organizational excellence.

Key Responsibilities

• Conduct biocompatibility and toxicology evaluations in compliance with ISO 10993 standards and global regulatory requirements (FDA, EU MDR, China, Japan, etc.).

• Lead impact assessments of manufacturing, supplier, and material changes related to product biocompatibility and safety.

• Collaborate with internal teams including R&D, Regulatory Affairs, Quality, and external laboratories or CROs to plan, execute, and interpret biocompatibility testing, including chemical characterization studies.

• Develop and maintain biological evaluation plans (BEP) and biological evaluation reports (BER) to support regulatory activities.

• Coordinate and review biocompatibility testing performed by external laboratories, ensuring timely completion and accurate interpretation.

• Draft and defend biocompatibility sections of regulatory submissions and technical documentation.

• Maintain detailed records of biocompatibility data, studies, and assessments in accordance with internal SOPs and international regulations.

• Support internal SOP development and continuous improvement activities related to biocompatibility and toxicology.

• Engage with external standards organizations, participate in industry groups, and stay current on evolving biocompatibility requirements.

Qualifications & Skills

• Bachelor’s degree in biomedical engineering, biology, biochemistry, toxicology, analytical chemistry, materials science, or related field required. Master’s degree or higher preferred.

• 5+ years (for Bachelor’s degree holders) of experience in biocompatibility assessment of medical devices.

• Extensive knowledge of ISO 10993 standards, with proven experience applying these standards in a regulated environment.

• Experience with global regulations including FDA, EU MDR, REACH, and other international requirements.

• Strong project management skills with the ability to lead cross-functional teams and external partners.

• Excellent verbal and written communication skills.

• Familiarity with statistical analysis and Microsoft Office suite.

Nice to Have:

• Board Certified Toxicologist (DBTA) or equivalent qualification.

• Experience supporting product stewardship or environmental compliance activities.

• Knowledge of biocompatibility and toxicology considerations in product development and lifecycle management.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, please email the Employee Health Support Center ( [email protected] ) or contact AskGS to be directed to your accommodation resource.

The anticipated base pay range for this position is :

The anticipated base pay range for this position is $115,000 to $197,000 annually

Additional Description for Pay Transparency:

The Company maintains highly competitive, performance-based compensation programs. Under current guidelines, this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation’s performance over a calendar/performance year. Bonuses are awarded at the Company’s discretion on an individual basis. · Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance. · Employees may be eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)). · Employees are eligible for the following time off benefits: o Vacation – up to 120 hours per calendar year o Sick time - up to 40 hours per calendar year; for employees who reside in the State of Washington – up to 56 hours per calendar year o Holiday pay, including Floating Holidays – up to 13 days per calendar year of Work, Personal and Family Time - up to 40 hours per calendar year · Additional information can be found through the link below. The compensation and benefits information set forth in this posting applies to candidates hired in the United States. Candidates hired outside the United States will be eligible for compensation and benefits in accordance with their local market.