CLIENT CANNOT SPONSOR/TRANSFER WORK VISA AUTHORIZATION
Manage site-wide Quality Systems programs and team responsible for driving quality activity and compliance including managing audits, document control, NC/CAPA and post-market surveillance activity.
Requirements
Bachelor's degree in life sciences or related field preferred
10+ years' experience in a regulated industry, preferably Medical Devices or Pharma
5+ years in Quality or Regulatory Affairs
3+ years managing staff
Experience with FDA Part 820, Part 1271, ISO 13485, or AATB standards
Experienced in supporting NC/CAPA and audit responses
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Sr. Quality Systems Manager • Gainesville, FL, United States