Apply now Regulatory Affairs Associate I Date Sep 22 2025 Location Navi Mumbai India 400706 Company Teva Pharmaceuticals Job Id 64000 Who we are 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 opportunity Providing regulatory support for European and International Markets RA How you ll spend your day Completion of designated projects and tasks supporting European Market RA and International Market RA according to internal Work Instructions with guidance and direction by the manager and more senior colleagues Maintaining related documentation and regulatory IT systems in line with internal procedures Timely task completion in line with Work Instructions with accurate tracker updates and adherence to compliance standards Communication with Teva units across Europe and International Markets with 3rd Parties and with related Health Authorities Fulfilling other allocated department duties and ad-hoc tasks as directed by senior regulatory affairs staff Completion of trainings assigned in Teva internal learning management system within defined timeframes Attending team meetings and providing regular updates on the assigned activities and tasks to the manager and or to senior regulatory affairs staff Maintaining and developing awareness of the current pending regulatory legislation and guidelines Your experience and qualifications Qualification Masters in Pharmacy or Masters in Science Life Sciences College or University degree or equivalent work experience that provide knowledge of and exposure to fundamental theories principles and concepts Experience 2-3 years of experience in the Pharmaceutical Industry ideally within Regulatory Affairs but R D Development or QA would be considered Experience of regulatory documentation within Europe and or International Markets Knowledge Work experience involving core regulatory concepts and procedures Ability to use existing internal procedures to solve routine or standard problems Proficient in regulatory IT systems to support compliance and documentation processes Working knowledge of Office-365 applications and Veeva Vault systems Solid focus on Compliance and regulatory standards Basic knowledge of project management principles and tools Strong organizational skills to meet self team and company goals Ability to identify a problem or need for decision that exceeds the competence of the individual French and or German language proficiency will be an added advantage 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 We are committed to a diverse and inclusive workplace for all If you are contacted for a job opportunity please advise us of any accommodations needed to support you throughout the recruitment and selection process All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience Apply now