- Responsible for lot disposition of IMP e.g. drug product and active pharmaceutical ingredients- Ensure that the quality of produced IMPs, manufactured by Technical Research and Development in in accordance with cGMP regulations- Act as Quality single point of contact for the TR&D Teams for early stage products

- Development and integration of an agile low volume packaging department to process low order sizes.- Set up of a self-directed organization for low volume packaging operations- Responsible for defining lean packaging processes by challenging existing ways of working and introducing innovative solutions- Provide Quality Assurance-Oversight and take on role as a Quality Subject Matter Expert for diverse launches and projects.- Provide support in organizational topics and in… Show more - Development and integration of an agile low volume packaging department to process low order sizes.- Set up of a self-directed organization for low volume packaging operations- Responsible for defining lean packaging processes by challenging existing ways of working and introducing innovative solutions- Provide Quality Assurance-Oversight and take on role as a Quality Subject Matter Expert for diverse launches and projects.- Provide support in organizational topics and in shaping of the QA organization as a member of the Leadership Team in QA Finished Goods Show less

- Responsible for overseeing the release operations of manufactured batches and qualityoversight for the packaging department.- Establish a team environment by sharing recognition, providing feedback and supporting interdepartmental goals- Develop and maintain effective communication with stakeholders and business partners- Presentations and active participation in diverse inspections by health authorities including FDA

- Responsible for overseeing the release operations of manufactured batches and qualityoversight for the packaging department.- Establish a team environment by sharing recognition, providing feedback and supporting interdepartmental goals- Develop and maintain effective communication with stakeholders and business partners- Presentations and active participation in diverse inspections by health authorities including FDA

- Subject Matter Expert for quality relevant questions and quality business partner for thesterile packaging department and its interface functions.- Release of finished - and semi-finished products- Processing of deviations, market-complaints and GMP issues- Participation at external audits and health authority inspections in order to ensure GMP relevant requirements- Quality expert within local projects and product transfers

Performed patient counseling (e.g. developed medication plans together with physicians / HCPs)- Ensured supply of medicines to patients at weekends and during night shifts- Organized personal scheduling to ensure uninterrupted operations

Pharmacy practical training for the third German state examination, consulting customers and manufacturing of drug products.

Pharmacy practical training in the Department Clinical Manufacturing Parentals within Pharma Global Technical Operations.