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Technician (m/f/d) MS&T Process Analytical Technologies

Date: Jul 12, 2019

Location: Ulm, DE, 89079

Company: Teva Pharmaceuticals

Company Info

Teva is a global pharmaceutical leader and the world’s 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 world’s largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we’ve 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!

Job Description

The candidate (m/f/d) will be a member of Bio Manufacturing Sciences and Technology group (MS&T) within the Global Operations organization at Teva. The MS&T departments, USP, DSP and Analytics are designated to facilitate the handover of production processes from biologics R&D to commercial production. This includes scale-up/scale down of processes, support of process transfers and process validation, optimization / continuous improvement and troubleshooting activities.

  • Performing diverse analytical tasks in the MS&T Analytics laboratory
  • Supporting the analytical team in bioanalytical method development, validation and transfer focused on but not limited to electrophoretical and immunological methods
  • Supporting setup of a bioanalytical laboratory unit including qualification and acquisition of new analytical instruments
  • Supporting, maintenance and qualification of analytical systems, such as balances, pipettes, cIEF, etc.
  • Performing analyses of in-process samples, finished products to assess the quality
  • Writing of scientific and technical reports
  • Author, modify and review standard operating procedures associated with the laboratory routine and support systems
  • Be part of a team for continuous processes / methods improvement, troubleshooting and deviations investigation in collaboration with the relevant commercial manufacturing site (in-house or 3rd party)
Qualifications
  • Vocational training (e.g. biological lab assistant,  chemical lab assistant (BTA, CTA) or related)  or BSc in Biotechnology, Biochemistry or Molecular Biology or related field
  • General understanding of the principles and hands on experience with electrophoretical and immunological techniques and equipment (SDS-PAGE, Western Blot, ELISA, CE, cIEF or cSDS) are required
  • Basic knowledge of working principles in GLP (Good Laboratory Practice) and/or GMP (Good Manufacturing Practice) environment would be a plus
  • Experience in method development/validation/transfer would be an advantage
  • Good command of German and English (spoken and written) required
  • Intermediate skills of MS Office (Word, Excel, Power Point, MS Project)
  • Team player with excellent organizational and communication skills, experience with multicultural environment
  • Good organizational skills with ability to organize and prioritize his/her work independently

Please include your cover letter and CV in English.

Contact Person

Julita Mlynska
Human Resources
0049 699 675 84 20
 

Function
Manufacturing
Sub Function
Technical Transfer
Teva’s 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, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.