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Biocompatibility & Materials Scientist, Insulin Infusion

Job in Los Angeles, Los Angeles County, California, 90079, USA
Listing for: Mini Med
Full Time position
Listed on 2026-06-12
Job specializations:
  • Engineering
    Biomedical Engineer, Research Scientist, Materials Engineer, Medical Device Industry
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below

About The Role

Mini Med is seeking a highly experienced Distinguished Scientist with specialized expertise in biocompatibility, materials science, and chemistry to advance the development of next‑generation medical devices. This senior technical leader will provide strategic direction for the biological safety, compatibility, and performance of patient‑contacting materials and components, ensuring the delivery of safe, reliable, and innovative infusion technologies and devices.

Impact

This role serves as a senior technical leader in advancing biocompatibility and materials innovation for next‑generation medical devices. The individual will define and lead scientific strategies for the biological safety, compatibility, and performance of materials, coatings, polymers, and component chemistries used in infusion sets and patient‑contacting device applications.

Leveraging deep expertise in biocompatibility and materials science, this leader will enable the development of safe, reliable, and scalable solutions that enhance extended‑wear performance, patient comfort, and overall device reliability. The role will have significant impact on long‑term technology strategy, portfolio roadmaps, and product innovation by translating scientific insights into practical, regulatory‑compliant medical device solutions that strengthen Mini Med’s competitive position.

Subject

Matter Expertise

Recognized technical expert in biocompatibility, materials science, and chemistry for patient‑contacting medical devices, with deep knowledge of biological safety evaluation for materials, coatings, polymers, and fluid‑path chemistries used in infusion technologies. Brings strong expertise in ISO 10993‑based biocompatibility strategy, material and chemical characterization, extractables/leachables assessment, and evaluation of material interactions affecting extended‑wear performance, patient comfort, and insulin stability. Applies scientific leadership to translate emerging materials and chemistry innovations into scalable, regulatory‑compliant device solutions, while influencing technology strategy, cross‑functional decision‑making, and portfolio innovation.

Responsibilities
  • Lead biocompatibility strategy, including comprehensive biocompatibility assessments, for materials and components used in Mini Med insulin infusion and medical device technologies.
  • Lead materials innovation efforts to enable extended‑wear infusion sets and improve long‑duration performance in subcutaneous environments.
  • Provide technical leadership in material characterization, chemical characterization, and extractables/leachables assessments.
  • Evaluate the compatibility of materials, coatings, and fluid‑path chemistry with insulin and extended‑wear device requirements.
  • Identify and advance innovative materials solutions that improve safety, reliability, comfort, and product performance.
  • Translate early‑stage research and emerging scientific opportunities into scalable, manufacturable, and compliant product solutions.
  • Partner closely with cross‑functional teams including R&D, clinical, regulatory, quality, toxicology, and manufacturing.
  • Build and engage in external partnerships with suppliers, universities, research institutes, and contract laboratories to evaluate emerging technologies and accelerate innovation.
  • Contribute to scientific leadership and innovation through patents, publications, technical forums, and external engagement.
  • Mentor and develop technical talent while strengthening scientific capabilities across the organization.
  • Provide oversight for biocompatibility test execution and documentation to ensure alignment with regulatory expectations and good documentation practices.
Requirement Qualifications
  • Requires a bachelor’s degree and 15 years of experience or a master’s degree and 13 years of experience, or a PhD with at least 10 years of relevant experience.
Preferred Qualifications
  • Master or PhD in Materials Science, Polymer Chemistry, Biomedical Engineering, Chemical Engineering, or a closely related field.
  • Master’s degree in science or engineering with a minimum of 13 years of medical device or combination product development experience, or a PhD in…
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