24.04.24 | Vollzeit | Hamburg | Coloplast Distribution GmbHEDC, Hamburg, reporting directly to the Operational Excellence Manager. - Drive and manage Excellence Organization within the EDC in alignment with EDC Management and Global Distribution Lean Management - Ensure state-of-the-art performance data management, especially quality-related KPIs - Maintain
Später ansehen26.04.24 | Vollzeit | MED-EL Medical ElectronicsAnd processes that impact speed to value and time to market - Leading analyses of business capabilities, business needs against provided solution to identify gaps Your Profile - Familiarity with information management practices, system development life cycle management, IT services management, agile and lean
Später ansehen26.04.24 | Vollzeit | Hanau | HGA - Gesundheitsakademie HessenSustainability Management & Leadership Projektmanagement Good Manufacturing Practice (GMP) KI in der biologisch-pharmazeutischen Industrie Führungskräfte Seminare Kursdauer 12 Wochen - optional 12 Wochen Traineeship Pharma Operations Management .erweitert den Kurs zusätzlich um das Thema Clinical Trial
Später ansehen23.04.24 | Vollzeit | Hamburg | Coloplast Distribution GmbHOf contact for process and technical matters - Manage development and execution of business transition management activities - Create, review and prioritize the setting of system requirements - Work closely with respective business units to implement an action plan - Measure and review success factors
Später ansehen23.04.24 | Vollzeit | Tübingen, Wiesbaden, Amsterdam | CureVac Corporate Services GmbHPolicies and procedures - Partner with teams to develop and implement risk-informed practices to address vulnerability assessments and mitigate potential weaknesses in systems - Work with managed services providers to ensure that information security practices are in place to identify, respond
Später ansehen24.04.24 | Vollzeit | Feldkirchen (Straubing-Bogen) | DanaherOr Master´s degree in Engineering - Science field • Over 6 years of experience in Quality Management Systems in a Pharma or Medical Device industry • Knowledge of ISO 13485, IVDR, 21 CFR Part 820 and 11 • Excellent Quality Documentation skills (Good Documentation Practices) • Ability to work independently
Später ansehen24.04.24 | Vollzeit | Markt Schwaben | DanaherOr Master´s degree in Engineering - Science field • Over 6 years of experience in Quality Management Systems in a Pharma or Medical Device industry • Knowledge of ISO 13485, IVDR, 21 CFR Part 820 and 11 • Excellent Quality Documentation skills (Good Documentation Practices) • Ability to work independently
Später ansehen24.04.24 | Vollzeit | Unterschleißheim | DanaherOr Master´s degree in Engineering - Science field • Over 6 years of experience in Quality Management Systems in a Pharma or Medical Device industry • Knowledge of ISO 13485, IVDR, 21 CFR Part 820 and 11 • Excellent Quality Documentation skills (Good Documentation Practices) • Ability to work independently
Später ansehen24.04.24 | Vollzeit | Starnberg | DanaherOr Master´s degree in Engineering - Science field • Over 6 years of experience in Quality Management Systems in a Pharma or Medical Device industry • Knowledge of ISO 13485, IVDR, 21 CFR Part 820 and 11 • Excellent Quality Documentation skills (Good Documentation Practices) • Ability to work independently
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