Working for CDMO projects & QA Systems

• QA support and strong involvement in a multidisciplinary team for projects with pharmaceutical customers (contract manufacturing of drug substances/API or GMP Intermediates)
• Handling of various Customer Requests
• Management of Quality Agreements to improve performance and customer satisfaction
• Responsible for project related deviation and complaint management and follow up the corresponding corrective actions
• Perform Risk assessments (ICH Q3D, Nitrosamine, Process/ICH Q9)
• Work with a positive, hands-on attitude to support colleagues and ensure that processes are aligned with national and international standards

• Master degree in a relevant scientific or corresponding engineering discipline such as Chemistry or Pharmacy
• Proven experience in a GMP regulated industry such as API or pharmaceutical
• Must have the ability to simultaneously multi-task across multiple capabilities
• Very good language skills in German and English
• Good knowledge of MS Office