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Biocompatibility Engineer Jobs in California (NOW HIRING)

Cala Health

Senior Mechanical Design Engineer

San Mateo, CA · On-site

$102K - $141K/yr

... biocompatibility). * Quality & Rigor: Demonstrated experience with medical device phase-gate ... Education: BS in Mechanical Engineering or a related technical field. Cala Health believes our ...

Cellanome

Staff Scientist, Chemistry

Foster City, CA

$140K - $200K/yr

PhD in Chemistry, Chemical Engineering, Materials Engineering, Bioengineering, or a related ... Experience with biocompatibility evaluation of biomaterials. The estimated base salary range for ...

Intuitive

Senior Manager, Instruments

Sunnyvale, CA · On-site

Were a team of engineers, clinicians, and innovators united by one purpose: to make surgery smarter ... Expertise in biocompatibility principles and regulatory requirements, e.g. ISO 10993 * Knowledge of ...

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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 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?

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 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.
What cities in California are hiring for Biocompatibility Engineer jobs? Cities in California with the most Biocompatibility Engineer job openings:
Biocompatibility Engineer jobs near you
Infographic showing various Biocompatibility Engineer job openings in California as of July 2026, with employment types broken down into 2% Internship, 16% Full Time, 3% Part Time, 6% Temporary, 70% Contract, and 3% Nights. Highlights an 95% Physical, 2% Hybrid, and 3% Remote job distribution.

Staff Quality Engineer, Design Quality - Pleasanton, CA

Calyxo

Pleasanton, CA • On-site

$80K - $103K/yr

Full-time

Medical, Retirement, PTO

Re-posted 2 days ago

Job description

Calyxo, Inc. is a medical device company headquartered in Pleasanton, California, USA. The company was founded in 2016 to address the profound need for improved kidney stone treatment. Kidney stone disease is a common, painful condition that consumes vast amounts of healthcare resources each year. Our team is led by executives and investors with a proven track record of commercializing paradigm-shifting devices to meet unmet needs within urology.
Are you ready to change the future of kidney stone treatment? We are seeking high achievers who want to be part of a dynamic team working in a fun, diverse atmosphere.
Summary:
We are seeking a skilled and detail-oriented Staff Quality Engineer to join our New Product Development (NPD) team. This role is responsible for ensuring that our Class-II new products meet the highest quality standards throughout the development process, from concept to commercialization. The ideal candidate will have experience in the medical device industry and a strong understanding of quality engineering principles, design controls, project management, and regulatory requirements.
This role will focus on ensuring that quality is embedded in the design, development, and manufacturing of new medical devices. The ideal candidate will have a strong background in quality engineering within the medical device industry, with experience supporting Class-II or Class-III product development lifecycle and software development, from concept through commercialization.
In This Role, You Will:
  • Ensure design controls for new product development and improvement project activities, including risk management, design V&V, product software validation, design reviews, tagging/tracing, non-product tools validation, test method validation, and design transfer are in compliance with Calyxo Quality System, FDA 21 CFR Part 820, ISO 13485, ISO 14971, IEC 62304, IEC 60601, and relevant global regulations.
  • Drive risk management activities per ISO 14971, including risk management plan, hazard analysis, FMEAs (design, software, user), risk-benefit analysis, and risk management report.
  • Own and maintain design control documentation in compliance with ISO 13485 and 21 CFR Part 820.
  • Collaborate with R&D, PMO, Regulatory Affairs, and Manufacturing to ensure robust design inputs, outputs, traceability and quality considerations are integrated into all phases of the product development lifecycle.
  • Maintain accurate and up-to-date quality records, including test reports, validation reports, and risk management documentation. Prepare and present quality-related reports to management and project teams.
  • Promote a structured software development process in compliance with IEC 62304, assuring that a state of control is maintained with robust software risk management.
  • Support regulatory submissions (e.g., 510(k), CE Mark) by providing design assurance documentation and justifications.
  • Support sterilization assessments as per ISO 11135 EO and ISO 11137 radiation requirements.
  • Support biocompatibility assessments as per ISO 10993 requirements.
  • Lead root cause investigations and corrective actions related to design-related issues.
  • Mentor junior engineers and promote a culture of quality and continuous improvement.
  • Stay current with evolving regulatory standards and industry best practices.
  • Collaborate with R&D to achieve electrical safety and EMC certification.
  • Partner with supplier quality team and new suppliers to ensure that components and materials meet specified quality standards. Participate in supplier qualification and audit processes as needed.
  • Support complaints investigations, NCs and/or CAPA related to NPI complaints post-launch.
  • Conduct DHF audits at each phase to ensure phase deliverables are complete.
  • Review and approve engineering documentation, test protocols, and reports to ensure compliance and technical integrity.
  • Identify opportunities for continuous improvement in product design and manufacturing processes.
  • Lead or participate in initiatives to enhance product quality, reduce costs, and improve overall efficiency

Who You Will Report To:
  • Director, Design Quality Assurance

Requirements:
  • Bachelor's degree in Engineering, Biomedical Engineering, Mechanical Engineering, Systems Engineering or a related technical field.
  • Minimum 10 to 12+ years of experience in quality engineering within the medical device industry, with strong record of being a vital part of NPD launch.
  • Strong knowledge, applications, and subject matter expertise of ISO 13485, ISO 14971, IEC 62304 and FDA 21 CFR Part 820.
  • Excellent presentation skills and proactive leading mindset. Effective communication, collaborative attitude, and strong accountability mindset.
  • Detailed understanding of design controls, risk management, and process validation in the context of medical device development from concept to feasibility to V&V to design transfer to launch.
  • Experience with systems design verification and validation (V&V) activities, including support for development of test protocols and reports.
  • Hands-on experience working with FMEA tools (design, software, user).
  • Excellent problem-solving skills, with the ability to analyze complex technical issues and develop effective solutions. Proficient in statistical tools applications such as Minitab, Jump etc.
  • Detail-oriented, with a commitment to producing high-quality work and maintaining rigorous documentation.
  • Certifications such as ASQ CQE (Americal Society for Quality Certified Quality Engineer), ASQ CSQE (Certified Software Quality Engineer), Six Sigma Black Belt or similar are a plus.
  • Work location: Pleasanton, CA.
  • Travel: 5-10% domestic travel may be required.
  • Full time employment.
  • Must be able to lift 10-15 pounds and sit for up to 8 hours/day.
  • Compliance with relevant county, state, and Federal rules regarding vaccinations.
  • Hybrid 4 days/week onsite, 1 day remote.

What We Offer:
At Calyxo, you will be part of a knowledgeable, high-achieving, experienced and fun team. You will work in a diverse work environment with experienced, proven leaders and have an opportunity to shape our company culture. You will experience constant learning and dynamic challenges to help you grow and be the best version of yourself.
We also offer an attractive compensation package, which includes:
  • A competitive base salary range of $170,000 - $185,000 and variable incentive plan
  • Stock options - ownership and a stake in growing a mission-driven company
  • Employee benefits package that includes 401(k), healthcare insurance and paid vacation

Calyxo is deeply committed to fostering an environment where diversity and inclusion are not only valued but also prioritized. We believe a diverse and inclusive community empowers us to act courageously, care deeply, and dream boldly to impact people in big ways. Diverse viewpoints bring diverse capabilities, which strengthen our focus and fuel our growth.
Calyxo is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment. All applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status or any other applicable legally protected characteristics
Legal authorization to work in the United States is required. In compliance with federal law, all persons hired will be required to verify their identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire.
Disclaimer:
At Calyxo, we prioritize a transparent and structured interview process to ensure the best fit for both our candidates and our team. Please be aware of the following:
  • Structured Interview Process: Our hiring process includes multiple stages of interviews where you will have the opportunity to communicate directly with Calyxo employees. This ensures that you gain a comprehensive understanding of the role and our company culture.
  • Verification of Identity: We do not extend job offers without first meeting candidates, either virtually or in person. This step is crucial to maintain the integrity of our hiring process and to ensure mutual alignment.
  • Beware of Scams: Calyxo will never request sensitive personal information, such as your full name, address, phone number, or identification documents, via email or online forms before an official interview. Calyxo representatives will always contact you using an email format of firstname.lastname@calyxoinc.com. If you receive a request for information from any other domain, please contact us directly at info@calyxoinc.comto verify the legitimacy of the communication.

We appreciate your interest in joining Calyxo and look forward to getting to know you through our official channels.

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