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Expert Stability (Temporary for one year)

Date: Nov 23, 2022

Location: Sofia, BG, 1407

Company: Teva Pharmaceuticals

Who are we?

 

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 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. As a Teva company, in October 2020 Actavis has started the process of re-branding and anticipating the Teva brand.

 

We are looking for qualified and motivated candidate for the role of Expert Stability (Temporary for one year) based in Sofia.

 

Main 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 EMSO Quality EMEA:
•    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 Compliance team

Audits/inspections:
•    Participation in the preparation of the department for audits and inspections
Change Control/Compliance:
•    Support in ensuring of change control process with regards to stability where applicable
Tech transfer / switches/launches:
•    Support during processes of transfers, switches and launches of the product with regards of ensuring high quality of the product
Assurance of pharmaceutical quality:
•    Support in processing of critical quality issues aroused during inspections at manufacturers or 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 EMSO with respect to stability 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 stability related 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

 

Main requirements

 

•    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
•    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 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 other flexible benefits
•    Flexible working hours and option to work from home as per the company policy
•    Opportunity for development

 


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.

 

Function

Quality

Sub Function

Supplier Quality

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.