BSc Life Science Jobs at Novartis | Apply Now For The International Program Regulatory Manager (IPRM) Role
Novartis is hiring an International Program Regulatory Manager (IPRM) in Hyderabad, India. This role offers the opportunity to contribute to global and regional registration strategies, ensuring efficient execution of regulatory plans across International (INT) markets. If you are passionate about regulatory affairs and aspire to make a difference in global healthcare, this position at Novartis could be the right step for your career.
- Job Position: International Program Regulatory Manager (IPRM)
- Location: Hyderabad, India
- Job ID: REQ-10058981
About Novartis
Novartis is a leading pharmaceutical company with a mission to reimagine medicine, improving and extending people’s lives. Our vision is to become the most valued and trusted medicines company in the world. We are committed to fostering a diverse and inclusive work environment where individuals can thrive and make a difference in patients’ lives.
Job Description
The International Program Regulatory Manager (IPRM) supports the International Program Regulatory Director (IPRD) in executing registration plans, monitoring country requirements, and ensuring compliance across INT markets. The role includes maintaining regulatory databases, driving initiatives to enhance efficiency, and supporting emerging market brand strategies. The IPRM may also act as deputy to the IPRD on assigned programs and global RA sub-teams.
Key Responsibilities
- Provide input into registration strategies and ensure execution of plans in collaboration with international teams.
- Contribute to dossier preparation, responses to Health Authority (HA) queries, and milestone follow-ups.
- Maintain updated country contact lists and regulatory databases.
- Partner with RA roles to obtain, analyze, and share pipeline information.
- Support the execution of emerging market brand strategies and registration plans for INT-specific diseases.
- Drive dissemination of country requirements to global roles.
- Act as deputy of IPRD on select programs.
- Support cross-functional initiatives to improve efficiency and resource allocation.
Qualifications
- Degree in Science (Chemistry, Pharmacy, Biochemistry, Biotechnology, Biology, or equivalent).
- Minimum 2 years of experience in regulatory affairs (country, regional, or global).
- Strong knowledge of regulatory license maintenance and new product registrations.
- Project management experience with cross-functional collaboration skills.
- Proven ability in risk assessment and regulatory issue resolution.
- Highly committed, organized, and a strong team player.
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