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Associate Director, Preclinical Toxicology
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- Associate Director, Preclinical Toxicology
- Your Role: The Associate Director of Preclinical (Toxicology and biocompatibility) will support a portfolio of drug, medical device, drug packaging system, and/or combination product development and global registration.
- The role will report to Director of Preclinical and Toxicology assessment team responsible drugs and devices for Peritoneal dialysis, Hemodialysis, and Acute therapies ($5B product portfolio with global reach in more than 100 countries).
- Independently develops and authors responses to submission deficiencies/questions (e.g., 510K, PMA, EU MDR).
- Must possess a working knowledge of toxicology and preclinical regulatory requirements as they relate to the development and registration of medical devices and an eagerness to learn and develop scientific competence beyond their current skills.
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