This position will function within the Toxicology Unit of Corporate Preclinical Development and Toxicology (CPDT) and will support the conduct of nonclinical laboratory investigations of medical devices and materials by GLP regulations and the BD CPDT Quality System.
Education/Experience:
Minimum 5 years of industrial experience in Medical device risk assessments.
Toxicology background required
Responsible for data analysis
Biocompatibility experience required
A minimum of Bachelor's degree is required but preferred someone who has a Master's or Ph.D., in science background