The Biocompatibility Project Analyst supports nonclinical laboratory investigations of medical devices in accordance with GLP and ISO 17025 regulations within BD’s Corporate Preclinical Development and Toxicology department
Job Summary
The Biocompatibility Project Analyst supports nonclinical laboratory investigations of medical devices in accordance with GLP and ISO 17025 regulations within BD’s Corporate Preclinical Development and Toxicology department.
Responsibilities include managing test sample inventory, coordinating testing activities, collaborating with project managers and toxicologists, and assisting with final documentation to meet FDA and international regulatory requirements.
BD values a culture of learning, growth, and accountability and requires most roles to have a minimum of 4 days in-office presence per week to foster collaboration and innovation.
Matching Summary
The Biocompatibility Project Analyst supports nonclinical laboratory investigations of medical devices in accordance with GLP and ISO 17025 regulations within BD’s Corporate Preclinical Development and Toxicology department.