Role Summary
Principal Research Scientist I, Tissue Material Sciences Fillers. Leads research and project activities within the Tissue Materials Science group, mentoring scientists and driving multi-disciplinary strategies for the Fillers device franchise (including Juvéderm and Next Generation Dermal Fillers). Focus areas include interactions of devices with cells/tissues, device proof of concept, regulatory submission studies (ISO 10993), life cycle compliance, and scientific messaging for advertising/promotional support. Acts as a team leader, engaging stakeholders across global marketing, medical affairs, regulatory, clinical development, and publications.
Responsibilities
- SCIENTIFIC LEADERSHIP
- Function as a principal investigator/lead, generating original technical ideas and research or development strategies.
- Represent TMS in cross-functional teams to provide technical leadership for design, analysis and reporting for pre-concept or development programs and drive alignment with functional management.
- Authors publications, presentations and/or primary inventor of patents.
- Serve as a technical advisor and subject matter expert in the discipline.
- May mentor/train/manage junior staff in a matrix-based organization or as part of a project team.
- SCIENTIFIC EXECUTION
- Demonstrate creative thinking to solve difficult problems and champion new technologies to achieve project goals.
- Develops and executes in vitro, in vivo and tissue processing methods to support development of novel medical device/tissue products.
- Critically evaluate scientific or regulatory advances, threats or business opportunities.
- SCIENTIFIC COMMUNICATION
- Serve as a technical advisor and subject matter expert to management and internal customers, aligning with cross-functional Asset teams.
- May contribute to publications, regulatory documents and inventions and present at external conferences.
- Provide regular updates to management and project teams; prepare technical reports as needed.
- CROSS-FUNCTIONAL TEAM REPRESENTATION
- Key team member in Asset Strategy, developing project strategy.
- Represent TMS on Asset/Strategy/product development subteams; provide expertise on tissue responses to Fillers.
- Support Design Control activities as non-clinical representative with minimal guidance.
- Organize and participate in project meetings; communicate status to supervisors and R&D committees.
- Prepare time/cost estimates for project activities to meet realistic completion dates.
Qualifications
- Education: Ph.D. with 6+ years of industry experience, or Master’s with 12+ years, or Bachelor’s with 14+ years in a related scientific or engineering discipline (cell biology, molecular biology, pharmacology, immunology, bioengineering, etc.).
- Medical device experience or regulated environment experience preferred.
- Experience in medical device, pharmaceutical, or related R&D settings with a track record of successful projects.
- Working knowledge of medical device, drug and/or biologics regulations (e.g., 21 CFR 820, 210/211, Part 4, Biologics).
- Experience managing outsourced research activities; managing in vivo and in vitro studies.
- Knowledge of biocompatibility testing requirements (ISO 10993); biocompatibility study experience is a plus.
- Technical report writing for regulatory submissions; experience with animal models and imaging.
- Strong communication, leadership, and collaborative skills; ability to multitask and meet deadlines; ability to build cross-functional relationships; mentoring capability.
Skills
- Original technical idea generation and research/development strategy.
- Cross-functional collaboration and project leadership.
- In vitro/in vivo method development; tissue processing; biocompatibility knowledge.
- Technical writing, presentations, and regulatory documentation.
- Mentoring and senior technical advisor capabilities.
Education
- Ph.D. in a related field or equivalent combination of education and experience as detailed above.