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Senior Manager MSAT (m/f/d)

Date: Jan 11, 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


You will be a member of Bio Manufacturing Sciences and Technology group (MS&T) within Teva 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 and continuous improvement activities. Part of your role will be scientific supervision of an analytical team for method development UPLC/HPLC (SEC, IC, IEX, RP, glycans). You will be developing the analytical laboratory including equipment procurement and qualification &. are also the main professional point of contact for HPLC/HPLC-MS technologies in local and global project teams. Additional experience in HPLC-MS technologies is a plus.


Other responsibilities include:


  • Method development, transfer and validation according to ICH guidelines
  • Active collaboration with R&D, commercial production and contract labs
  • Responsible for laboratory safety and routine maintenance
  • Preparation of development reports and regulatory documentation as required for submissions



  • Diploma or Master´s degree in Biochemistry, Biology, Biotechnology, Pharmacy, Life Sciences or equivalent ideally with PhD
  • Minimum of 3 years relevant experience (pharmaceutical-/ biotech- industry or contract research organization) in laboratory management and analytical sciences and 2+ years’ experience in a supervisory/leadership position.
  • HPLC or HPLC-MS working experience in a GxP lab environment and knowledge of applicable regulations would be a plus
  • Additional professional knowledge in glycan analysis or CE or cIEF would be a plus
  • Experience and knowledge in operation of modern LC and mass spectrometry platforms as well as associated data analysis packages
  • Teamplayer with excellent organizational and communication skills.
  • High degree of self-organization and proactive mindset
  • Very good skills on MS-office applications
  • Good command of German and English (spoken and written)
  • Experienced in collaboration within international organizations



Sub Function

Technical Transfer

Reports To

In process of validation

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.