Teva Pharmaceutical Industries Ltd in Malta is looking to recruit a Regulatory Affairs Associate to join their team within their Regulatory Affairs team on a full-time basis. The ideal candidate will report to the Sr Mgr Regulatory Affairs.
This position is mainly responsible for supporting the company to obtain and maintain marketing authorisations for EU and Growth Markets, by actively participating in the change control system, by providing regulatory expertise and support in order to avoid any production disruption while maintaining compliance. The main activities include but are not limited to keeping the dossiers (Module 3 and QoS) fully up to date in compliance with the latest regulatory requirements, preparing the necessary documents in support of dossier and variations submissions and responding to queries from Competent Authorities during Marketing Authorisation or Variation procedures.
Teva Pharmaceutical Industries Ltd:
Teva Pharmaceutical Industries Ltd. is a leading global pharmaceutical company that delivers high-quality, patient-centric healthcare solutions used by millions of patients every day. Headquartered in Israel, Teva is the world’s largest generic medicines producer, leveraging its portfolio of more than 1,800 molecules to produce a wide range of generic products in nearly every therapeutic area. In speciality medicines, Teva has a world-leading position in innovative treatments for disorders of the central nervous system, including pain, as well as a strong portfolio of respiratory products. Teva integrates its generics and speciality capabilities in its global research and development division to create new ways of addressing unmet patient needs by combining drug development capabilities with devices, services and technologies. Teva's net revenues in 2017 were $22.4 billion.
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