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Nabídka volných pracovních míst

Zentiva, the generics business of the Sanofi group, is the third largest and fastest growing generics company in Europe based in Prague. Zentiva currently operates in 35 countries in Europe, Africa and the Middle East, and its products are used by almost 800 million people. We are at the forefront of developing modern, high-quality and affordable medicines. As a fast-growing company we are looking for talented and ambitious individuals who will help drive the development of our Company and achieve our objectives.
We are looking for a suitable candidate for the position:

Quality Management - System development Manager

Job purpose:

  • Creation, development and further lifecycle management of corporate Quality Management System within whole company
  • To assure effectiveness of the Quality Management System with international as well as local pharmaceutical regulations and company operative needs in all GxP areas
  • Acting as focal point for all company end users of electronic document management system as well as users of manual document management system in case of training, technical support in eDMS, or troubleshooting

Your responsibilities:

  • Creation, developing and further maintaining of Quality Management System and corresponding documentation up to date
  • Writing, revision , approval and issuance of GxP relevant corporate guidelines within company QMS
  • Training of all eDMS end users and allocation of right access rights
  • Management of all changes relating to system workflow development, or upgrade
  • Setup communication network and way of working with manufacturing sites, affiliates and corporate teams
  • To review, comment and approve each corporate policy, or guideline within GxP environment and in line with approval flow.
  • To review effectiveness of all QMS documents with owners. To initiate, or coordinate regular revisions and archiving
  • To coordinate and review implementation of corporate policies and guidelines at manufacturing sites, affiliates and corporate teams
  • To prepare regular reporting in respective area
  • Acting as qualified GMP auditor for all entities within the company

We require:

  • Technical University Degree (health, pharma, chemical areas are advantage)
  • Experience in pharma quality (corporate organizations are advantage)
  • Knowledge of GxP regulations
  • Experience in internal/external auditing
  • English language in writing and speaking
  • Ability to learn / quick adaptability / analytical /organized / communicative
  • Independant professional role with ability to lead transversal teams

We offer:

  • Find the way to your happiness at work
  • An opportunity to further growth within company structure
  • An opportunity to broaden your knowledge and expertise in your field
  • Continuous language and personal development
  • An attractive compensation & benefits package
  • 10,000 CZK in the Flex program for the calendar year
  • Flexible working hours and 1day/week home-office option
  • Subsidized meals in our company dining room
  • Work place: Prague 10, Dolni Mecholupy


Karolína Korsesková
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