Assist the site CAPA owners, investigators and approvers on each and every CAPA, provide training and guidance, and monitor every CAPA at each phase
Job Summary
Assist the site CAPA owners, investigators and approvers on each and every CAPA, provide training and guidance, and monitor every CAPA at each phase.
Promote/ Leading / mentoring / conducting quality improvement projects thru continuous improvement initiatives and may obtain Green/Black Belt Certification.
BD is committed to providing a robust set of value-based programs and resources that are best-in-class, market-competitive and affordable for all associates and their families.
Matching Summary
Assist the site CAPA owners, investigators and approvers on each and every CAPA, provide training and guidance, and monitor every CAPA at each phase.
Skills & Requirements
Must-have
CAPA process ownership
Quality System understanding
Continuous improvement initiatives
Regulatory compliance leadership
Medical device manufacturing experience
Nice-to-have
Mentoring quality improvement projects
Fostering creativity and innovation
Human element across global teams
High performing work teams
Key Requirements
5 years manufacturing experience
3 years CAPA Process experience
2 years Quality manufacturing experience
Proven history of product/process improvements
Ability to generate validation protocols
3 years practical GMP/Medical Device manufacturing experience