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Expert Quality Services

Date: Jan 16, 2021

Location: Sofia, BG, 1407

Company: Teva Pharmaceuticals

Company Info


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 August 2016 Actavis has been acquired by Teva Pharmaceutical. In Bulgaria, we are the largest employer in the pharmaceutical industry, with nearly 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. As a Teva company, in October 2020 Actavis has started the process of re-branding and anticipating the Teva brand.


We are looking for a motivated and solution oriented candidate to become a part of our BG Quality Services, TPO Quality team on the position of Expert Quality Services, based in Sofia. The role is responsible to ensure a high quality of TPO products, which comply with national law and internal guidelinesand to support of decision processes with expert knowledge in regards to Raw materials, Stability Management, Cost control, PQRs.

Key Responsibilities


·    Stability
Support in activities related to Studies performed during stability control including studies performed in internal Teva sites or external studies performed in Vendor’s or contract labs
·    Support within Quality TPO European Generics
Support in obtaining of product-related reports to QA/QPs or team leaders in case of quality deviations during the active stability studies in order to take decisions with regard to usage, necessary actions for product optimization and variations if applicable in collaboration with Quality Complience team.
·    Audits/inspections
Participation in the preparation of the department for audits and inspections.
·    Raw Materials
Support in fulfillmet of quality relevant requests from contract manufacturers and internal departments with regard to raw materials used in the manufacturing of pharmaceutical products at external sites in both cases when Teva or Vendor is responsible for quality oversight of the raw materials. 
·    Change Control / Compliance
Support in ensuring of change control process with regards to stability and raw materials where applicable.
·    Tech transfer / switches / launches
Support during processes of transfers, switches and launches of the product with regards of ensuring hight quality of the product.
·    Assurance of pharmaceutical quality
Support in processing of critical quality issues aroused during inspections at manufacturers or anounsed by GNTM of raw materials and stability. Support for evaluation and examination of affected products and quality issues in close cooperation with QA/QP.
·    Projects
Assistance in realization of global projects at TPO with respect to raw materials, stability and cost control for quality services. Support the team leaders and qualified persons in the development of adequate concepts to meet project objectives and timelines.
Processing of resulting tasks inclusive of monitoring and communication of project progress.

·    Cost Control
Support in requesting of POs for Quality services and following activities in accordance with internal approved processes and guidelines.
·    PQRs
Support to the relevant team for the periodical evaluation with regard to the PQR process and of KPIs

Education, experience and abilities


·    Master's degree, preferably in Chemistry, Pharmacy, or related natural sciences
·    2+ years experience in the field of quality control with regard to Stability testing, Raw materials
·    Knowledge about analytical methods and technics.
·    Knowledge of production steps and the resulting manufacturing descriptions
·    Good software knowledge of MS-Office, SAP Business Warehouse and Trackwise
·    Good command of the written and spoken English language
·    Good communication and relationship skills
·    Ability to solve problems

We offer


·    Dynamic and challenging job in a highly professional international environment
·    Opportunity to work in a global project based environment
·    Attractive remuneration package and performance related bonuses


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

All personal data is protected by law and will be treated in confidentiality. 

Only short-listed applicants will be contacted.

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.