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Leiter der Herstellung (w/m/d) / Associate Director (f/m/d)

Singen (Hohentwiel), Germany

Overview

Every day, employees working in Takeda’s Global Manufacturing and Supply Chain, and Global Quality business unit are shaping the future of healthcare. They are breaking down barriers and ensuring our life-changing medicines are available, accessible, and affordable to patients. Life-changing for you. Life-changing for patients.

Global Manufacturing and Supply Chain, and Global Quality is the backbone of Takeda, and our employees are the guardians for our patients, our products, and our reputation. As a member of our team, we can offer you the opportunity to grow in a meaningful career, develop your skills, and come to work every day knowing that what you do makes a genuine difference.

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Success

What makes a successful member of our team? Check out the traits we’re looking for and see if you have the right mix.

  • Agile
  • Ambitious
  • Analytical
  • Collaborative
  • Enthusiastic
  • Entrepreneurial

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Opportunity

  • Bold initiatives, continuous improvement, and creativity are at the heart of how we bring scientific breakthroughs from the lab to patients.

  • Here, you will feel welcomed, respected, and valued as a vital contributor our global team.

  • Through trust and respect, you will have genuine support from leaders, managers, and colleagues to do your best work.

  • A strong, borderless team, we strive together towards our priorities and inspiring mission.

  • Recognized for our culture and way of working, we’re one of only 13 companies to receive Top Global Employer® status for 2018.

  • Our people-first mission extends beyond patients to include their families, communities, and our own Takeda family.

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Leiter der Herstellung (w/m/d) / Associate Director (f/m/d)

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Job ID R0010534 Date posted 08/14/2019 Location Singen (Hohentwiel), Germany

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Job Description

For English see below.

Ihre Aufgaben

  • Leitung der Abteilung aseptische Produktion TSI/LY des Takeda Standorts Singen
  • Verantwortung für die Mitarbeiter und  Prozesse bei der Herstellung und Abfüllung eines sterilen Lyophilisats, sowie mehreren sterilen Liquida im vollkontinuierlichen Schichtbetrieb
  • Verantwortlich für die erfolgreiche Restrukturierung des Produktionsbereichs im Hinblick auf Arbeitsabläufe, Technologie und Produkt Portfolio
  • Budget- und Personalverantwortung für ca. 100 Mitarbeiter
  • Überwachung und Dokumentation aller für die Herstellung und Abfüllung nötigen Abläufe unter möglichst effizienter Nutzung der Ressourcen und Einhaltung der cGMP Standards für aseptische Produktion
  • Kontinuierliche Optimierung der Produktionsprozesse
  • Permanente Reduktion der Abweichungen 
  • Ausarbeitung von Herstellungsprotokollen und SOPs
  • Aufrechterhaltung des GMP-Compliance-Status
  • Durchführung regelmäßiger Personalschulungen
  • Enge Kooperation mit den anderen Abteilungen am Standort Singen

Ihr Profil

  • Abgeschlossenes Studium der Pharmazie, Mikrobiologie oder verwandte naturwissenschaftliche oder verfahrens-technische Gebiete
  • Fundierte Erfahrung im Produktionsumfeld der pharmazeutischen Industrie
  • Mehrjährige Führungserfahrung sowie Erfahrung im GMP Umfeld
  • Verhandlungssichere Englischkenntnisse
  • Ziel-, Ergebnis- und Kundenorientierung
  • Kommunikative Persönlichkeit mit Verhandlungsgeschick
  • Strukturiertes und zielorientiertes Arbeiten
  • Fähigkeit, komplexe Aufgabenstellungen klar zu organisieren und zu priorisieren

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Your Accountabilities

  • Head of the Aseptic Production department TSI/LY at Takeda's Singen location
  • Responsibility for the employees and processes involved in the production and filling of a sterile lyophilisate and a number of sterile liquids in fully continuous shift operation
  • Responsible for the successful restructuring of the production area in terms of workflows, technology and product portfolio
  • Budget and personnel responsibility for approx. 100 employees 
  • Monitoring and documentation of all processes required for production and filling, using resources as efficiently as possible and complying with cGMP standards for aseptic production
  • Continuous improvement of production processes
  • Continuous reduction of deviations  
  • Preparation of production reports and SOPs
  • Maintaining of GMP compliance status
  • Regular training of personnel
  • Close cooperation with the other departments at the Singen site

Your Profile

  • Completed studies in pharmacy, microbiology or related scientific or process engineering fields
  • Sound experience in the production environment of the pharmaceutical industry
  • Several years of management experience, as well as experience in the GMP environment
  • Business-fluent English
  • Focus on targets, results and customers
  • Communicative personality and skilled in communication
  • Structured, goal-oriented work methods
  • Ability to clearly organise and prioritise complex tasks

Takeda GmbH

Human Resources

Robert-Bosch-Str. 8,

78224 Singen, Germany

Tel. +49 7531-84 2108

www.takeda.de

Locations

Singen, Germany

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time

Job ID R0010534

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