Job Description

Who we are

Teva Pharmaceutical Industries Ltd. (NYSE and TASE: TEVA) is a global leader in generic medicines, with innovative treatments in select areas, including CNS, pain and respiratory. We deliver high-quality generic products and medicines in nearly every therapeutic area to address unmet patient needs. We have an established presence in generics, specialty, OTC and API, building on more than a century-old legacy, with a fully integrated R&D function, strong operational base and global infrastructure and scale. We strive to act in a socially and environmentally responsible way. Headquartered in Israel, with production and research facilities around the globe, we employ 40,000 professionals, committed to improving the lives of millions of patients. Learn more at

In Bulgaria, we are the largest employer in the pharmaceutical industry with near 1700 employees in the two manufacturing plants (Dupnitsa and Troyan); sales and marketing organization and in a number of global corporate functions based in our country. After the acquisition of Actavis by Teva Pharmaceuticals, in Bulgaria we are operating under the Teva brand.

We search for qualified and motivated candidate for the role of IT QA Expert , based in Sofia.

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

Enjoy a more rewarding choice

• Dynamic and challenging work environment in one of the world leading pharmaceutical company and the biggest pharmaceutical company in Bulgaria
• Competitive remuneration bound with performance
• Additional healthcare insurance
• Transportation allowance and additional flexible benefits
• Flexible working hours and option to work from home as per the company policy
• Opportunity for development

Make a difference with Teva Pharmaceuticals

If this sounds like the right opportunity for you, send us your CV in English.
Please, kindly note that only shortlisted applicants will be contacted. All personal data is protected by law and will be treated in confidence.

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.

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