QA Supervisor

SCOPE OF THE POSITION/RESPONSIBILITIES:

Work together to manage the corporate Quality System as delegated by the QA TT & Deviations Head.

SPECIFIC TASKS/PRIMARY ACTIVITIES:

In relation to the Department requirements and based on the instructions of the QA TT & DeviationsManager, work directly in the operative contexts listed below and manage the assigned resources for these activities, which he/she supervises:

• Corporate quality complaints, defining contingent solutions and plans of action that avoid the recurrence of problems raised
• Drafting the Annual Product Review
• Deviation and Investigation Management regarding quality issues
• Managing the CAPA system deriving from quality investigations
• Preparing periodic quality trends for Management and to share with Corporate
• Support for Operational Excellence initiatives

• Degree in Biology, Pharmacy, CTF, Chemistry or another scientific discipline
• GMP Regulations (EU, USA)
• MS Office Package
• 5 years of experience as an individual contributor in QA or Pharmaceutical Production
• Plus at least 5 years of leadership experience
• Fluent English

• Personal development
• International experience
• Great work atmosphere
• Fixed term contract