YOUR TASKS AND RESPONSIBILITES

• Drive GMP projects for production solids
• Be responsible for GMP compliance for all HVAC, media and utility systems
• Drive risk assessments
• Drive root cause analysis of system relevant deviations
• Support process validation as well as (re)-qualification
• Be responsible for updating and launching new SOPs
• Be responsible for initiating and driven change request
• Process of system critical deviations

WHO YOU ARE

• University degree as pharmacist (m/f/d), PhD desirable
• Long-term professional experience in pharmaceutical quality/production/development incl. leadership skills
• Profound knowledge in the areas of GMP, qualification, validation and documentation
• Critical judgement and analytical skills
• Very good organization, cooperation and communication skills as well as ability to work in a team
• High degree of independence, reliability, persuasiveness and flexibility
• Fluent in German and English, both written and spoken