Job Information
Teva Pharmaceuticals IT QA Expert in Sofia, Bulgaria
IT QA Expert
Date: May 10, 2024
Location:
Sofia, Bulgaria, 1407
Company: Teva Pharmaceuticals
Job Id: 55822
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 www.tevapharm.com.
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.
EOE including disability/veteran