Mgr Regulatory Affairs

1 day ago

India Teva Full time ₹ 12,00,000 - ₹ 24,00,000 per year

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 International Markets RA.
  • Coordination of assigned regulatory activities.
How you'll spend your day
  • Completion of designated projects and tasks supporting International Market RA, according to internal Work Instructions, with moderate level of guidance and direction by the manager.
  • Coordination, prioritization, planning and monitoring the tasks related to assigned regulatory activities.
  • Development/maintenance of the expertise and solving straightforward problems, related to assigned regulatory activities.
  • Maintaining related documentation and regulatory IT systems, in line with internal procedures.
  • Communication with Teva units across Europe and International Markets, with 3rd Parties and with related Health Authorities.
  • Guiding and supporting more junior team members.
  • 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.
  • Maintaining and developing awareness of the current/pending regulatory legislation and guidelines
Your experience and qualifications
  • 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.
  • 10+ years of experience in the Pharmaceutical Industry, ideally within Regulatory Affairs
  • Experience of regulatory documentation within Europe and/or International Markets.
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.

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