This role is responsible for the technical oversight and continuous improvement of document and change management processes within the Quality Management System
Job Summary
This role is responsible for the technical oversight and continuous improvement of document and change management processes within the Quality Management System.
The position requires managing internal and external audits while developing strategic corrective action plans to address root causes of issues.
BD offers a culture that values authentic self-expression, accountability, and learning to help reinvent the future of health.
Matching Summary
This role is responsible for the technical oversight and continuous improvement of document and change management processes within the Quality Management System.
Skills & Requirements
Must-have
10 years QMS administration experience
8 years medical device industry experience
Document control and change management expertise
Audit management and CAPA implementation
Electronic documentation system administration
Nice-to-have
Cross-functional collaboration skills
Strategic corrective action planning
Engaging training curriculum design
Data-driven quality improvement
Subject Matter Expertise in QMS
Key Requirements
Bachelor's degree in engineering, life sciences, or related field
Minimum 10 years of experience with QMS administration
At least 8 years of medical device or life science industry experience
Demonstrated experience in managing audits and CAPAs