Description:

The Director, Quality Management System is responsible for standardization and proactive compliance of Amneal's QMS with the worldwide drug, biologics and combination products regulations and standards. This role is responsible for compliance monitoring, compliance risk identification, quality plan for new requirements, site inspection readiness, and regulatory authority (FDA, …) inspection support.

Essential Functions:

Lead network wide regulatory commitments monitoring and implementation of associated corrective and preventive actions (CAPAs). Identify compliance risks and implement corrective and preventive actions. Support external audits and inspections from regulatory agencies. Co-ordinate with site leaders in addressing inspection findings including draft response. Implement quality system compliance intelligence enabling proactive monitoring of changes in the worldwide drug, biologics, device regulations and guidance. Review of changes in regulations, gap assessment, development of action plan, and implementation. Interpret and communicate regulatory requirements to internal stakeholders. Participate in internal audits to ensure compliance with GMP, GCP, GLP, and other applicable standards. Analyze current industry compliance trends and Amneal sites’ compliance ratings to establish compliance risks.