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Manufacturing Science and Technology Specialist (MS&T Specialist)

Date: Jan 9, 2021

Location: Troyan, BG, 5600

Company: Teva Pharmaceuticals

Company Information


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. 


Teva is looking for ambitious and motivated candidates for the position of MS&T Specialist, based in Troyan manufacturing site. 


The Role


The MS&T Specialist will be responsible for new product transfers, technological process transfer and validation of new generic products and adapts the production processes with the pharma equipment at the Production facility, ensuring that activities meet required deadlines.


Main responsibilities


•    Provide knowledge and experience in the areas of formulation and process development, transfer and optimization of new generic products in compliance with the modern high standards of the pharmaceutical industry 
•    Optimize technological processes and solve queries related to the production, participate in validation documentation  preparation
•    Manage and control manufacturing product lifecycle, generate and review required technological /validation documentation per regulatory requirements as needed
•    Provide knowledge and experience in the application of experimental design concepts to process development optimization and robustness studies.
•    Responsible for completing all training requirements 
•    Responsible for maintaining work areas and performing job functions in a safe and efficient manner in accordance with company policies and procedures, Good Manufacturing Practices (cGMP’s), Standard Operating Procedures (SOP’s) 

Requirements to the candidates


•    University degree in Pharmacy, Chemistry or Masters of Pharmacy will be considered as an advantage
•    Previous experience in processing equipment and technologies utilized in Good Manufacturing Practices(GMP) will be considered as an advantage
•    Ability to interact positively and collaborate with colleagues 
•    Analytical, innovative and create thinking 
•    Ready to learn and develop
•    Very good English skills both written and spoken
•    Very good computer literacy – MS Office package

We Offer


•    Dynamic and challenging work environment in a highly motivated team of professionals
•    Competitive remuneration bound with performance
•    Food allowance
•    Job specific training
•    Opportunity for development in an international company
•    Included transportation from certain locations


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 candidates 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.