Expert Registration

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 45,000 professionals, committed to improving the lives of millions of patients.

Since August 2016, Actavis has been part of Teva. In Bulgaria the combined company is working under the Actavis brand and is the largest employer in the pharmaceutical industry. Actavis - a Teva company - manages two manufacturing plants, sales and marketing organization and a number of global corporate functions.

For the manufacturing site in Dupnitsa, we are looking for an Expert of Registration.

Main responsibilities:

● Responsible for all prepared registration documentation related to medical products in Bulgaria and abroad in terms of required regulation.
● Prepare documents for pre-registration and amendments to the Marketing Authorization of medical products in Europe and other countries.
● Answer all questions from Medicinal Agencies.
● Monitor all procedures for concerned parties
● Evaluate every change from the manufacturing site and submit the required documents
● Prepare CDI (Core Data Information) for changes from the suppliers of active substances.
● Liaise with and communicate the tasks to all colleagues within the company.

Successful candidates should have:

● Preferred Master’s degree in Pharmacy, Chemistry or Biology
● 5 years of working experience in the manufacturing field of pharmaceutical products
● Knowledge of Medicinal Law of Human Medicine
● In-depth knowledge of regulatory requirements for medicine products in Europe and all other countries
● Very good computer literacy, with MS Office
● Advanced English language level – writing and speaking
● Experience in dynamic work environments with Teva group members from all over the world

What the company could offer you:

● Specific training in accordance with the job responsibilities
● Working in a modern and high-tech work environment
● Stability and long-term employment
● Opportunities for professional development
● Organized transport from Sofia, Blagoevgrad, Kyustendil, Pernik

If this sounds the right opportunity for you, send your CV and Cover letter in English not later than 18.10.2018, via -