.Together, we're on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It's a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world's leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization's Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we're always looking for new ways to continue making a difference, and new people to make a difference with.The opportunityTo lead and proactively manage all regulatory activities associated with development, registration and maintenance of Drug Master Files according to current international regulatory requirements.Your experience and qualificationsEducation: High degree in relevant field, e.G. chemistry/biochemistry/biology or biotechnologyConversational English and at least 5 years of experience according to the minimum requirements below:Support the life cycle management of APIs from RA perspectiveReview and approve ROS, specification and analytical control when requiredCoordinate DMF preparation and related activities for On Time Submissions for all relevant marketsProactively collaborate with the Regulatory Specialist team members, which support the submission or answer service requestsPrepare a DMF specific high level gap analysis report and proactively communicate any risk to the relevant departments. Follow up on the gaps' solving during the review periodRespond to deficiency letters and coordinate related activitiesCoordinate pre-launch activities from RA perspectiveManage the regulatory aspects and related tasks of the assigned commercial APIsEvaluate change requests and address the required submission per market to support the requested change. Follow through the submissionMaintain up to date the DMFs according to the required regulation of updating per marketSupport customers regarding Service Requests, giving relevant professional information in the shortest of timeContinue learning of regulatory guidance, SOPs and work processesMake a difference with Teva PharmaceuticalsReports ToSr Mgr Regulatory AffairsTeva's Equal Employment Opportunity CommitmentTeva 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. We are committed to a diverse and inclusive workplace for all