Regulatory Professional I Job at Novo Nordisk in Bangalore at Novo Nordisk for experienced regulatory affairs professionals in global pharmaceutical operations.
Company: Novo Nordisk
Job Title: Regulatory Professional I
Category: Regulatory Affairs & Safety Pharmacovigilance
Team: International Operations Regulatory Affairs
Location: Bangalore, Karnataka, India
Work Location: Novo Nordisk Global Business Services (GBS), India
Job Type: Full-Time, Permanent
Experience Required: 5+ Years
Application Deadline: February 4, 2026
Application Mode: Online
About the Company
Novo Nordisk is a global healthcare company with a more than 100-year legacy of innovation, scientific excellence, and commitment to improving patient lives. Headquartered in Denmark, Novo Nordisk is a world leader in diabetes care and has strong positions in obesity, rare diseases, and other serious chronic conditions. Regulatory Professional I Job at Novo Nordisk
Driven by a single purpose—to defeat serious chronic diseases—Novo Nordisk combines cutting-edge research, sustainable business practices, and a deep sense of responsibility toward patients and society. The company operates in more than 80 countries and serves millions of patients worldwide.
Novo Nordisk Global Business Services (GBS) in India plays a vital role in supporting global operations by delivering high-quality services across regulatory affairs, safety, quality, clinical development, and commercial functions. Employees at Novo Nordisk work in a culture defined by respect, diversity, curiosity, and a shared passion for making a meaningful difference in healthcare. Regulatory Professional I Job at Novo Nordisk
Job Details
- Job Title: Regulatory Professional I
- Function: Regulatory Affairs & Safety Pharmacovigilance
- Team: International Operations Regulatory Affairs
- Location: Bangalore, Karnataka, India
- Workplace: Novo Nordisk Global Business Services (GBS)
- Employment Type: Full-Time, Permanent
- Experience Level: Mid-Senior
- Application Deadline: February 4, 2026
This role is part of Novo Nordisk’s International Operations Regulatory Affairs organization and supports regulatory activities across multiple international markets. Regulatory Professional I Job at Novo Nordisk
Job Description
As a Regulatory Professional I at Novo Nordisk, you will be responsible for securing regulatory approvals for new products and lifecycle management activities across International Operations. The role involves managing regulatory submissions, coordinating with health authorities and distributors, maintaining regulatory systems, and ensuring compliance with country-specific regulatory requirements. Regulatory Professional I Job at Novo Nordisk
You will work closely with global and regional stakeholders, affiliates, and external partners to ensure high-quality, timely regulatory deliverables. This position requires strong regulatory knowledge, excellent communication skills, and the ability to work in a complex, cross-functional, international environment.
This opportunity is ideal for experienced regulatory affairs professionals who want to contribute to global product approvals and lifecycle management in a highly respected pharmaceutical organization. Regulatory Professional I Job at Novo Nordisk
Key Responsibilities
As a Regulatory Professional I, your responsibilities will include: Regulatory Professional I Job at Novo Nordisk
- Securing regulatory approvals for new products, including New Drug Applications (NDA) and Lifecycle Management (LCM) licenses, within agreed timelines for assigned countries
- Managing end-to-end product lifecycle activities, including regulatory submissions, renewals, variations, and post-approval changes
- Reviewing submission packages and preparing regulatory application forms in accordance with country-specific health authority requirements
- Coordinating and engaging with distributors, affiliates, and local health authorities to ensure timely approvals and regulatory compliance
- Handling regulatory documentation required for tenders and other country-specific submissions
- Updating regulatory systems, including Veeva Vault, with product dossiers, submission statuses, and approval information within defined timelines
- Collaborating with affiliates to develop and review product labelling materials in line with local legislation
- Reviewing promotional materials to ensure compliance with regulatory requirements, internal SOPs, and local laws
- Monitoring local regulatory environments and assessing the impact of regulatory changes on existing and upcoming products
- Ensuring ongoing regulatory compliance for marketed products across assigned countries
- Providing regulatory support for post-approval activities and regulatory signals
- Supporting health authority interactions and ensuring responses align with country-specific requirements
- Contributing to continuous improvement of regulatory processes and documentation quality
- Working cross-functionally with quality, supply chain, clinical, safety, and commercial teams as required
Required Qualifications
Novo Nordisk is looking for a highly motivated and proactive regulatory professional with the following qualifications: Regulatory Professional I Job at Novo Nordisk
Educational Qualification
- Post-Graduation or equivalent degree in Science, Pharmacy, Life Sciences, or a related discipline
Experience Requirements
- Minimum 5+ years of experience in Regulatory Affairs within the pharmaceutical industry
- At least 3+ years of experience working with key stakeholders and decision-makers outside India in an international, cross-functional environment
- Experience working in an affiliate environment and shared service model is preferred
- Hands-on experience handling interactions and conversations with health authorities
- Experience supporting regulatory submissions across multiple international markets
Regulatory Professional I Job at Novo Nordisk
Skills and Competencies
- Strong understanding of global regulatory frameworks and health authority requirements
- Experience in regulatory submissions for NDAs, variations, renewals, and lifecycle management activities
- Familiarity with regulatory information management systems such as Veeva Vault
- Excellent documentation, review, and compliance skills
- Strong stakeholder management and communication abilities
- Ability to work effectively in a multicultural, international environment
- Basic project management skills with the ability to manage multiple priorities simultaneously
- High attention to detail and strong quality mindset
- Ability to work independently while collaborating with global teams
Regulatory Professional I Job at Novo Nordisk
About the Department
The International Operations Regulatory Affairs – Bangalore (IORA Bangalore) team is a critical extension of Novo Nordisk’s global IOSO Regulatory Affairs organization based in Zurich and Copenhagen. Regulatory Professional I Job at Novo Nordisk
The team delivers core regulatory capabilities that enable fast portfolio growth, business continuity, and high-quality product approvals across International Operations. IORA Bangalore consists of highly skilled regulatory professionals who work collaboratively to support regulatory submissions, compliance, and lifecycle management activities at scale.
By joining this team, you will contribute directly to Novo Nordisk’s mission of delivering safe, effective, and compliant medicines to patients worldwide. Regulatory Professional I Job at Novo Nordisk
Working at Novo Nordisk
At Novo Nordisk, employees are driven by a shared purpose and a commitment to making a difference. The company fosters an inclusive and diverse workplace where every individual is respected and encouraged to grow. Regulatory Professional I Job at Novo Nordisk
Novo Nordisk values curiosity, collaboration, and accountability. Employees are empowered to challenge conventional thinking, explore innovative solutions, and continuously develop their professional capabilities. The organization’s long-term vision focuses on sustainable healthcare solutions that create lasting impact for future generations.
When you join Novo Nordisk, you become part of a global legacy dedicated to improving lives and shaping the future of healthcare. Regulatory Professional I Job at Novo Nordisk
Why You Should Join Novo Nordisk
- Opportunity to work with a globally respected pharmaceutical leader
- Exposure to international regulatory operations and global health authority interactions
- Strong focus on quality, compliance, and professional development
- Collaborative and inclusive work culture
- Long-term career growth opportunities in regulatory affairs
- Meaningful work contributing to patient health worldwide
Regulatory Professional I Job at Novo Nordisk
FAQs
Is this a permanent role?
Yes, this is a full-time permanent position.
Is international regulatory experience required?
Yes, experience working with international stakeholders and health authorities is required.
What systems will I work on?
You will work with regulatory systems such as Veeva Vault.
Is this an on-site role?
Yes, the role is based at Novo Nordisk Global Business Services in Bangalore.
What is the application deadline?
The application deadline is February 4, 2026.
How to Apply
Interested candidates should submit their application online by uploading an updated CV through the official Novo Nordisk careers portal. Follow the instructions provided in the job listing to complete your application.
Novo Nordisk does not charge any fees or request payments during the recruitment process. Candidates are advised to remain vigilant against fraudulent job offers.
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