Novonordisk is hiring for Regulatory Affairs Professionals | B Pharm & M Pharm Graduates | Apply Now
Looking for a Regulatory Affairs Job in the pharmaceutical industry? This Pharma Job at Novo Nordisk for the role of Associate Regulatory Affairs I in Bangalore is an excellent opportunity for professionals with regulatory experience. This Regulatory Affairs Job offers exposure to clinical trial approvals, lifecycle management, and regulatory submissions, making it a highly valuable Pharma Job for candidates aiming to grow in a global healthcare company.
- Position: Associate Regulatory Affairs
- Location: Bangalore, India
About the Company
Novo Nordisk is a leading global healthcare company with over 100 years of innovation in the treatment of serious chronic diseases. Headquartered in Bagsværd, the company is widely recognised for its strong focus on diabetes care, obesity treatment, and other chronic conditions.
Novo Nordisk has built a strong global presence, reaching millions of patients worldwide and impacting more than 40 million lives daily. The company is known for developing life-changing medicines, particularly in areas like insulin therapy and modern biologics.
Key Responsibilities
- Prepare and submit clinical trial applications and related documents to health authorities.
- Manage trial maintenance activities, including renewals, updates, and amendments.
- Support submissions for new products, medical devices, and lifecycle variations.
- Handle safety information, lifecycle changes, and labelling/artwork workflows.
- Maintain accurate records, trackers and ensure timely archiving of submissions.
- Provide regulatory intelligence and keep stakeholders updated on local requirements.
- Coordinate with local authorities (e.g., State FDA) as required.
- Ensure compliance with company procedures, ethical standards, and the Novo Nordisk Way.
Qualifications
- A bachelor’s degree in pharmacy (or similar), and a Master’s degree in Pharmaceutical Regulatory Affairs is considered an advantage.
- At least 2 years of experience within regulatory affairs or a related role in the pharmaceutical industry.
- Knowledge of clinical trial application processes and product lifecycle maintenance activities.
- Strong attention to detail, good planning skills and the ability to manage multiple priorities.
- Clear communication skills and a collaborative mindset, with commitment to high ethical standards.
Application Last Date
- 27th March 2026
