Specialist QA Compliance (m/f/d)

Your Profile:

• Master's degree preferrably in Life Sciences or related field
  
• Minimum of 5 years relevant experience in a GxP regulated pharmaceutical/biotechnology industry
  
• Solid computer skills including MS Office required / SAP, LIMS, Quality Management Systems skills are a plus
  
• Analytical thinking and problem-solving attitude
  
• Multilingual - at least German and English, written and spoken

Your Tasks:

• Reviews and approves deviations, investigations, CAPAs and Change Controls
  
• Reviews and approves process validation documents including risk assessments
  
• Oversees site manufacturing activities (oral and parenteral)
  
• Establishes annual Product Quality Reviews
  
• Ensures regulatory compliance and continuously improves the allocated quality systems and procedures
  
• Participates in audits and inspection within the area of responsibility

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