Senior R&D Scientist, Biomaterials

Job Overview

The Sr. Engineer Material/Bio Science plays a critical role in advancing orthopedic medical device technologies through materials science and biological evaluationexpertise. This position contributes directly to product development innovation and lifecycle support by applying deep technical knowledge to ensurematerialsperformance biocompatibility safety and regulatory compliance. The role offers the opportunity to influence nextgeneration solutions that improve patient outcomes while collaborating across R&D Quality Regulatory and Manufacturing teams.

Key Responsibilities

• Lead and support materials and biological evaluations for orthopedic medical devices including metals polymers ceramics and coatings.

• Design plan and execute laboratory studies to assess material properties biocompatibility and performancein accordance withinternal standards and global regulations.

• Provide technicalexpertiseand guidance to crossfunctional teams throughout product development and lifecycle management.

• Interpret and document experimental data; author technical reports protocols and regulatory submissions.

• Support root cause investigations and materialrelated risk assessments for product or process issues.

• Contribute to theselection qualification and characterization of new materials and suppliers.

• Ensure compliance with applicable quality system requirements industry standards and regulatory expectations.

• Mentor junior engineers and contribute to continuous improvement and innovation initiatives.

Qualifications

Education

• Bachelors degree in Materials Science Biomedical Engineering Bioengineering Chemistry ora relatedscientific or engineering discipline (required).

• Masters or PhD in Materials Science Biomaterials ora relatedfield (preferred).

Experience and Skills

Required:

• Typically requires46yearsof relevant engineering or scientific experience aligned with a seniorlevel individual contributor role.

• Demonstratedexpertisein materials science and/or biomaterials for medical devices or regulated products.

• Experience designing and interpreting laboratory or preclinical studies.

• Strong technical writing skills including reports and regulatory documentation.

• Working knowledge of ISO ASTM FDA and other applicable regulatory standards.

• Ability to work independently while collaborating effectively in crossfunctional teams.

Preferred:

• Experience in orthopedic implantable or Class II/III medical devices.

• Handson experience with biocompatibility testing surface characterization or failure analysis.

• Familiarity with supplier qualification and materials change management.

• Experience mentoring or providing technical leadership to other engineers.

• Knowledge of statistical analysis and experimental design.

Other:

• Travel: Up to 10% (domestic) as needed.

• Language: English (fluent).

• Certifications: Relevant professional certifications (e.g. materials quality or regulatory)preferredbut not.

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