Senior Toxicologist
Core
Author scientifically rigorous Toxicological Risk Assessments (TRAs) for Class II/III medical devices and support regulatory submissions for respiratory care products.
Role type
Senior Toxicologist (Medical Devices)
Builds
Respiratory Care products (Sleep & Respiratory Care)
Domain
Healthcare Technology / Medical Devices / Toxicology
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Toxicological Risk Assessment (TRA) authoring, ISO 10993 and ISO 18562 compliance, in vitro and in vivo biocompatibility study interpretation, chemical characterization (VOCs, E&L), technical writing for regulatory submissions, cross-functional project management, CRO oversight
Preferred skills
Board Certification in Toxicology (DABT), experience with TRAs outside medical devices, AI tool usage for efficiency
Technologies
ISO 10993, ISO 18562, QMS documentation systems
Responsibilities
Author TRAs for medical devices, support design modifications and field issue assessments, interpret biocompatibility and chemical characterization data, update toxicology QSPs and WIs, represent Philips at scientific conferences
Seniority
Senior, hands-on IC
