IT QA Expert

Date:  Jul 19, 2024

Zagreb, Croatia, 10000

Company:  Teva Pharmaceuticals
Job Id:  56633

Who we are


Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.

The opportunity


The main purpose of this role in Global IT Quality and Compliance Operations is to work on IT projects to provide guidance and support for validation and compliance of the computerized systems in the process of the System Development Lifecycle (SDLC), and to review and approve all required validation deliverables by following applicable policies, standards and procedures.

How you’ll spend your day


  • Provide project validation support by assisting the creation and reviewing and approving all required validation deliverables from Quality perspective
  • Provide system life-cycle maintenance support by creating, reviewing, approving and maintaining validation deliverables from Quality perspective
  • Actively contribute to extend and preserve the Computer Systems Validation (CSV) knowledge in the Global IT Quality and Compliance Operations team and in the company
  • Support the CSV continuous improvement opportunities and knowledge-sharing
  • Provide local audit support
  • Support global supplier qualification process
  • Support procedures and guideline management
  • Support training management
  • Support inventory management
  • Support infrastructure qualification
  • Support IT Q&C process improvements

Your experience and qualifications


  • Master’s/Bachelor’s degree
  • Professional experience in CSV or SDLC activities and/or Quality Assurance (QA) or compliance activities in a regulated environment – at least 1 to 3 years
  • Experience in IT system implementation
  • A thorough knowledge of GxP compliance requirements of the European Medicines
  • Agency (EMA) and/or US Food and Drug Administration (FDA) and other international and national GxP regulations and guidelines to validation & compliance
  • A deep understanding of risk-based approach for validation and compliance activities
  • Orientation to achieving results and attention to detail
  • Excellent command of English
  • Strong interpersonal and communication skills
  • Excellent cooperation, analytical and presentational skills
  • Proven ability as a team player in an international work environment


If this sounds like the right opportunity for you, send us your CV in English.

Already Working @TEVA?


If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site


The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

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. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.