Regulatory Affairs Associate I (Maharashtra)

Regulatory Affairs Associate I (Maharashtra)

31 Jul
|
Teva Pharmaceuticals
|
Maharashtra

31 Jul

Teva Pharmaceuticals

Maharashtra

Apply now Regulatory Affairs Associate I Date Nov 20 2025 Location Navi Mumbai India 400706 Company Teva Pharmaceuticals Job Id 64983 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 current ways to continue making a difference and new people to make a difference with The opportunity To support the UK IE Regulatory Affairs Team with full administrative support in order to ensure full lifecycle management of Marketing Authorisations MA s tracking tools systems and databases are kept up to date Assist with all aspects of administrative management and equipment software inventories as required How you ll spend your day To work closely with the Line Manager to ensure completion of tasks within agreed timelines Monitor team inboxes where required Administrative support and preparation and management of Product Information in the Teva Document Management System To generate and submit simple variations label leaflet updates for approved UK IE products licences Provision of UK IE specific information and or documentation to EU Regulatory Affairs in support of new marketing authorisation applications and variation submissions Ensure that electronic files are up to date and maintained in accordance with Teva procedures Identify and escalate areas of administrative process improvement Accurately updating regulatory information systems following updates Provide support to the UK IE RA team for all projects which include specific documentation requests Proof reading of mock-ups ensuring compliance at all times Providing ad hoc support to requests from various department functions Administrative support for the cancellation process in accordance to internal processes Major Job Challenge s Meeting specific objectives whilst addressing frequent and often unscheduled issues and changing priorities To regularly discuss administrative workload and ideas for improving processes within the department and to request offer assistance where needed Working with a wide range of internal and external customers Your experience and qualifications Qualification M Pharma Experience 2 - 4 Years of experience in relevant pharmaceutical field Knowledge Basic understanding of processes and departments within a pharmaceutical company Microsoft Word Excel and Outlook Skills Excellent oral and written communication Ability to work under pressure and to tight time deadlines Effective time and organisation management Being able to work under your own Initiative and as part of a team Computer literacy Relationships Internal All personnel within UK IE Regulatory Affairs EU Regulatory Affairs Manufacturing QC testing and QA release sites Supply Chain and EDP Medical Affairs Medical Information and Pharmacovigilance Commercial Portfolio and Marketing Artwork Generation Groups Regulatory Information Management Team External Business Partners Customers Suppliers MHRA HPRA Reports To Associate Director Senior Manager or Manager Regulatory AffairsTeva 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

📌 Regulatory Affairs Associate I (Maharashtra)
🏢 Teva Pharmaceuticals
📍 Maharashtra

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