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Biocompatibility Engineer Jobs in California (NOW HIRING)

Abbott

Director, Biocompatibility

Santa Clara, CA · On-site

Integrate biocompatibility considerations early in product design, development, and lifecycle ... S. required in Biology, Biomedical Engineering, Materials Science, Toxicology, or related ...

Abbott

Director, Biocompatibility

Santa Clara, CA

Integrate biocompatibility considerations early in product design, development, and lifecycle ... S. required in Biology, Biomedical Engineering, Materials Science, Toxicology, or related ...

Remedy Robotics, Inc

Quality Engineer

San Francisco, CA · On-site

$160K - $220K/yr

We are looking to hire a Quality Engineer for our Hardware Team. What You'll Do: * Own the quality ... Exposure to biocompatibility and sterilization validation standards, including ISO 10993, ISO 11135 ...

Capstan Medical, Inc.

Quality Engineer

Santa Cruz, CA

$83K - $107K/yr

The Product Quality Engineer is responsible for providing quality engineering support to the ... Collaborate with R&D and Regulatory Affairs teams to ensure that biocompatibility requirements are ...

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Biocompatibility Engineer information

What is the difference between Biocompatibility Engineer vs Materials Scientist?

AspectBiocompatibility EngineerMaterials Scientist
Required CredentialsBachelor's or Master's in biomedical engineering, biology, or related fields; certifications in biocompatibility testingBachelor's or Master's in materials science, chemistry, or engineering; advanced degrees often preferred
Work EnvironmentMedical device companies, research labs, regulatory agenciesResearch institutions, manufacturing, aerospace, automotive industries
Industry UsageDesign and testing of biocompatible medical devices and implantsDevelopment of new materials for various applications, including medical, industrial, and consumer products

While both roles involve materials and testing, a Biocompatibility Engineer specializes in ensuring materials are safe for medical use, focusing on biological interactions. A Materials Scientist has a broader scope, working on developing and analyzing materials across multiple industries. The two roles often collaborate but serve distinct functions within product development and safety assurance.

What is a biocompatibility scientist?

A biocompatibility scientist is a professional who evaluates the safety of medical devices and materials by testing their interactions with biological systems. They often work in laboratories, using assays and standards such as ISO 10993 to assess potential adverse effects and ensure regulatory compliance.

Is there a demand for bioengineers?

There is strong demand for bioengineers, including biocompatibility engineers, due to the growth of the medical device and healthcare industries. These professionals are needed to develop and test biocompatible materials and devices, often requiring knowledge of materials science, biology, and regulatory standards. Job prospects are favorable with opportunities in research, development, and quality assurance roles.

Can a biomedical engineer make 200k?

Biomedical engineers, including biocompatibility engineers, can potentially earn $200,000 or more annually, especially with advanced experience, specialized skills, leadership roles, or working in high-paying industries like medical device manufacturing. Achieving this salary often requires a combination of advanced education, certifications, and years of experience in the field.

What does a Biocompatibility Engineer do?

A Biocompatibility Engineer is responsible for evaluating and ensuring that materials and devices intended for medical use are safe and compatible with biological systems. Their work involves assessing the interactions between medical devices and human tissues to prevent adverse reactions. They conduct laboratory tests, analyze data, and prepare technical documentation to meet regulatory standards. Biocompatibility Engineers play a crucial role in the development and approval of medical devices, working closely with regulatory agencies and product development teams.

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

To thrive as a Biocompatibility Engineer, you need a strong background in biomedical engineering or life sciences, with expertise in toxicology, materials science, and regulatory standards such as ISO 10993. Familiarity with laboratory testing protocols, risk assessment tools, and regulatory submission systems is typically required, and certifications like Certified Biological Safety Professional (CBSP) can be advantageous. Strong analytical thinking, meticulous attention to detail, and effective communication skills help in interpreting data, preparing reports, and collaborating with cross-functional teams. These competencies are crucial for ensuring medical devices are safe for human use and meet global compliance requirements.

What engineers make $500,000?

Senior engineers in specialized fields such as petroleum, aerospace, or software engineering can earn $500,000 or more annually, especially with experience, advanced skills, and bonuses. High-level roles often require advanced degrees, certifications, and leadership responsibilities within their industries.

What are some common challenges faced by Biocompatibility Engineers during the device development process?

Biocompatibility Engineers often encounter challenges in selecting appropriate materials that meet regulatory standards and ensuring compatibility with biological systems. They must navigate complex testing protocols and documentation requirements to demonstrate safety and effectiveness, which can be time-consuming and require cross-functional collaboration with regulatory, quality, and R&D teams. Additionally, staying updated with evolving international regulations and standards is vital, as non-compliance can delay product approvals and market entry.
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Biocompatibility Engineer jobs near you
Director, Biocompatibility

Director, Biocompatibility

Abbott

Santa Clara, CA • On-site

Full-time

Medical, Retirement

Posted 20 days ago

Abbott rating

7.9

Company rating: 7.9 out of 10

Based on 136 frontline employees who took The Breakroom Quiz

156th of 528 rated manufacturers

Job description

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries.
JOB DESCRIPTION:
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You'll also have access to:
  • Career development with an international company where you can grow the career you dream of
  • Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year
  • An excellent retirement savings plan with high employer contribution
  • Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor's degree
  • A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune
  • A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists

The Opportunity
The Director, Biocompatibility is responsible for providing strategic leadership and scientific direction for the global biocompatibility and materials safety program supporting medical devices and combination products. This individual will lead teams of scientists and toxicologists to ensure compliance with international biocompatibility, extractables and leachables, and materials characterization standards, while driving innovation and operational excellence in biological safety evaluation. The Director will serve as the company's subject matter expert and key liaison with regulatory agencies, internal stakeholders, and external partners on all matters related to biological evaluation and materials safety.
This position will be located in Santa Clara, CA or Saint Paul, Minnesota.
What You'll Work On
Strategic Leadership:
  • Develop and execute the global biocompatibility strategy aligned with business and regulatory objectives.
  • Provide scientific and regulatory leadership on biological safety and toxicological risk assessment for materials, manufacturing processes, and finished products.
  • Integrate biocompatibility considerations early in product design, development, and lifecycle management.

Team & Functional Management:
  • Lead and mentor teams of biocompatibility scientists across multiple sites.
  • Foster a culture of collaboration, accountability, and continuous improvement.
  • Oversee capacity planning, resource allocation, and performance management within the biocompatibility organization.

Regulatory & Compliance Oversight:
  • Ensure compliance with ISO 10993 and applicable global regulatory guidance.
  • Provide expert input for regulatory submissions (IDE, PMA, 510(k), CE, NMPA, etc.) and represent the function during audits and agency interactions.
  • Maintain strong awareness of evolving global biocompatibility and toxicology regulations and guide the organization in adapting accordingly.

Technical Leadership:
  • Oversee biological evaluation plans, toxicological risk assessments, and testing strategies for medical devices and combination products.
  • Collaborate closely with R&D, Quality, Regulatory, and Manufacturing to ensure material and process changes are biologically safe.
  • Guide biological evaluation programs for complex devices and combination products.

Cross-Functional Collaboration:
  • Partner with materials science, chemistry, and analytical testing teams to establish integrated strategies for material characterization and safety.
  • Serve as a key advisor to product development teams to enable safe, compliant, and efficient product launches.
  • Engage with external experts and standards organizations to influence future regulatory and technical frameworks.

Key Relationships:
  • The position interacts directly with functional groups including R&D groups, Preclinical, Regulatory, Analytical Chemistry, and Quality groups in the Abbott various business Divisions and CROs.

Qualifications
  • Bachelor's degree required
  • Ph.D. or M.S. required in Biology, Biomedical Engineering, Materials Science, Toxicology, or related discipline, preferably with a specialism relating to medical devices
  • Minimum of 12 years of relevant experience required in biocompatibility, toxicology, materials safety, or related within the medical device or combination product
  • Minimum of 5 years of leadership experience, including managing scientific teams and cross-site functions
  • Proven record of leading global biocompatibility or toxicology programs supporting regulatory submissions and product approvals
  • Expert in US and global regulations (e.g., EU, China, Korea and Japan) and requirements for biocompatibility and safety testing, particularly ISO 10993
  • Strong understanding of extractables and leachables, chemical characterization, and toxicological risk assessment methodologies
  • Excellent scientific judgment and strategic thinking
  • Exceptional communication, collaboration, and influencing skills
  • Demonstrated ability to lead in a global organization
  • Regulatory interaction experience (FDA, notified bodies, etc.) strongly preferred

APPLY NOW
Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com
Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal
The base pay for this position is
$172,000.00 - $344,000.00
In specific locations, the pay range may vary from the range posted.
JOB FAMILY:
Product Development
DIVISION:
MD Medical Devices
LOCATION:
United States > Santa Clara : Building B - SC
ADDITIONAL LOCATIONS:
United States > Minnesota> St. Paul > Woodridge : 177 East County Rd B
WORK SHIFT:
Standard
TRAVEL:
Yes, 20 % of the Time
MEDICAL SURVEILLANCE:
Not Applicable
SIGNIFICANT WORK ACTIVITIES:
Keyboard use (greater or equal to 50% of the workday)
Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.
EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf
EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf

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