Ihr Aufgabengebiet
- Overall responsibility for production under GMP conditions
- Management and further development of the sevenperson team
- Independent management and optimization of compliance and production processes
- Ensuring a troublefree production process during manufacturing
- Ontime provision of products in the required quality and quantity
- Reduction of rejects destruction and deviations
- Processing deviations in production in collaboration with quality assurance
- Ensuring the documentation of all production activities and maintaining GMP regulations
- Participating in the implementation of audits and inspections
Ihr Hintergrund
- Successfully completed studies in engineering process engineering mechanical engineering or comparable technical training
- Several years of professional experience in a production environment in the pharmaceutical biotech or food industry
- At least 3 years of management experience
- High level of problemsolving skills decisionmaking and assertiveness
- Ability to think holistically across departments
- Confident demeanor and strong communication skillsFluent written and spoken English
Ihre Benefits
- Modern and international working environment
- Pioneering work on a novel pharmaceutical product
- Plenty of room for professional development and creativity
- Flexible working hours with flexitime
- High worklife balance especially good compatibility of family and career
GenderHinweis
Aus Grnden der besseren Lesbarkeitwird auf die gleichzeitige Verwendungder Sprachformen mnnlich weiblichund divers (m/w/d) verzichtet.Smtliche Personenbezeichnungengelten gleichermaen fr alleGeschlechter.