29 days old

Senior Manager Quality Control (m/f/d)

Ulm, BW
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Company Info

Teva is a global pharmaceutical leader and the worlds largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide.  Our employees are at the core of our success, with colleagues in over 80 countries delivering the worlds largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and weve built a promising pipeline centered around our core therapeutic areas.  We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation.  This is how we improve health and enable people to live better, healthier lives.  Join us on our journey of growth!

Teva invests in a large scale mammalian API manufacturing facility in addition to the existing biotechnology production plant of its subsidiary Teva Biotech GmbH. The Sr Mgr Quality Control (m/f) will be responsible for all aspects of quality control within all project stages. As soon as the plant is going into operation he will be in charge of microbiological methods and equipment within his laboratory.

Job Description

  • Manage all activities within the group so that the sites quality control meets customer needs and objectives regarding quality, cost, service and safety
  • Translate production schedule to detailed work/sample analysis organization plan and ensure workflow optimization of analytical procedures and implement new methods/systems
  • Make sure analytical equipment is available, qualified and ready and support a culture of operational excellence for new equipment and methods for an efficient and effective environment
  • Ensure planning, controlling and documentation of transfer and validation of microbiological methods
  • Preparation and supervision of all relevant SOPs, specifications or other relevant procedures
  • Ensure regulatory compliance in the area of responsibility and appropriate GMP-documentation of all GMP related work within the group
  • Support the work for the design of the laboratory area, including analytical equipment and assist in pre-selection of appropriate suppliers for investments
  • Participate in internal and external audits form national and international authorities and supervise adequate CAPAs


  • PhD or Master degree in Microbiology and multi-year work experience in responsible role within microbiology, preferably experience in the realm of commercial biopharmaceutical API manufacturing with mammalian cell culture technology
  • Profound experience in microbiological methods for biopharmaceutical APIs and drug products including bioburden, sterility, mycoplasma testing, identification of microbes and fungi
  • Know-how in design of microbiological laboratories
  • Comprehensive knowledge of national and international GMP regulations
  • Experienced in leading a team
  • Fluent both in German and English
  • Ability to facilitate a team approach, to drive accountability, compliance and efficiency



Sub Function

Manufacturing Quality Control

Tevas Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.

Posted: 2018-12-21 Expires: 2019-02-18

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Senior Manager Quality Control (m/f/d)

Ulm, BW

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