BPharm Jobs at Novartis | Apply Now For The International Program Regulatory Manager Role

align: center;">BPharm Jobs at Novartis | Apply Now For The International Program Regulatory Manager Role

Novartis is hiring an International Program Regulatory Manager (IPRM) in Hyderabad, India. This role involves supporting international regulatory teams, driving execution of registration strategies, and ensuring timely delivery of registration plans across INT (International) markets. If you have experience in regulatory affairs, license maintenance, and new product registrations, this is your opportunity to work with a global leader in pharmaceuticals.

Job Details

  • Position: International Program Regulatory Manager (IPRM)
  • Location: Hyderabad, India
  • Job ID: REQ-10058981

About Novartis

Novartis is a leading global healthcare company with the vision to become the most valued and trusted medicines company in the world. The company reimagines medicine to improve and extend people’s lives, delivering innovative treatments to millions of patients worldwide. With a culture built on inclusion, diversity, and collaboration, Novartis provides its employees with opportunities to grow, thrive, and contribute to life-changing breakthroughs in medicine.

Job Description

As an International Program Regulatory Manager (IPRM), you will work under the supervision of the International Program Regulatory Director (IPRD) and collaborate with global, regional, and country regulatory teams. You will contribute to registration strategies, execution of regulatory plans, database management, and cross-functional initiatives. This role also involves supporting emerging markets and contributing to geographic expansion plans for Novartis products.

Key Responsibilities

  • Provide input into registration strategies and drive execution of registration plans in INT countries.
  • Support the IPRD by gathering, analyzing, and communicating pipeline information.
  • Maintain up-to-date registration databases and ensure timely updates with high quality.
  • Contribute to responses to health authority queries and dossier submissions.
  • Support efficiency initiatives and functional excellence within regulatory operations.
  • Drive the dissemination of information on international regulatory requirements to global stakeholders.
  • Act as deputy of IPRD on selected programs when required.

Qualifications

  • Degree in Science (Chemistry, Pharmacy, Biochemistry, Biotechnology, or Biology) or equivalent.
  • Minimum 2 years of experience in regulatory affairs (country, regional, or global).
  • Experience with regulatory license maintenance and new product registrations.
  • Strong project management, organizational, and problem-solving skills.
  • Ability to assess risks, recognize regulatory hurdles, and provide solutions.
  • Collaborative, team-oriented, and highly committed.

Benefits of Working at Novartis

  • Access to the Novartis Life Handbook covering rewards, health, and career benefits.
  • Inclusive and diverse workplace culture supporting equal opportunities.
  • Professional growth opportunities through cross-functional projects and global exposure.
  • Commitment to employee well-being and reasonable workplace accommodations.

APPLY ONLINE HERE

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