Regulatory Affairs Jobs at Novo Nordisk | BPharma Candidates Apply Now
Are you ready to contribute to a global healthcare leader that’s transforming chronic disease care? Novo Nordisk is hiring an Executive – Regulatory Affairs in Mumbai to support new drug submissions, regulatory compliance, and clinical development initiatives. If you have 3–5 years of experience in regulatory affairs within the pharmaceutical industry, this is your opportunity to play a pivotal role in shaping the future of healthcare.
About Novo Nordisk
Novo Nordisk is a leading global healthcare company with more than 95 years of innovation and leadership in diabetes care. Our mission is to drive change to defeat diabetes and other severe chronic conditions, such as obesity and rare blood and endocrine disorders. We strive to make a difference through our dedication to quality, scientific excellence, and patient-focused research.
Job Opening: Executive – Regulatory Affairs
Job Details:
- Location: Mumbai (Office)
- Employment Type: Full-time
- End Date to Apply: August 25, 2025 (26 days left to apply)
- Job Requisition ID: REQ-10058214
Job Description Summary:
HA submissions and regulatory compliances for New Drugs, Line extension, additional indication, production transfer, site registration, renewal, CMC, PI, PSUR to ensure business continuity and support clinical trial
projects under GDO. To oversee and drive compliance activities within CPO.Key Responsibilities:
- Compilation and HA submissions of New Drug applications, Line extensions, and additional indications.
- Development and implementation of regulatory strategy for pipeline products.
- Maintenance of compliance activities, such as PSURs and post-approval changes.
- Collaborate with local groups to ensure timely regulatory compliance.
- People management, process improvements, and support for audits and inspections.
Minimum Requirements:
- Degree in pharmacy, health discipline, or life sciences (minimum).
- 3-5 years in a relevant RA role in multinational companies.
- Good communication and interpersonal skills.
- Fluent in English, both written and spoken.
Why Novo Nordisk:
Our purpose is to reimagine medicine, improving and extending people’s lives. Join us in becoming the most valued and trusted medicines company in the world. Learn more: Novo Nordisk – People and Culture
Benefits and Rewards:
Find out more about our benefits and rewards in the Novo Nordisk Life Handbook.
Commitment to Diversity and Inclusion:
Novo Nordisk is committed to fostering an inclusive work environment and building diverse teams that reflect the patients and communities we serve.
Accessibility and Accommodation:
If you require accommodation due to a medical condition or disability during the recruitment process, please contact us at diversityandincl.india@novartis.com with your request. Don’t forget to include the job requisition number.
Keywords: Clinical Study Reports, Regulatory Affairs Jobs, Data Analysis, Documentation Management, Lifesciences, Job Posting, Operational Excellence, Regulatory Compliance
