Novo Nordisk Hiring Regulatory Professional I Opportunity in Bangalore

Regulatory Affairs Jobs at Novo Nordisk Bangalore | PG Science

Novo Nordisk hiring Regulatory Professional I in Bangalore. PG Science with 5+ yrs RA experience. Apply before 4 Feb 2026.

Novo Nordisk is inviting experienced regulatory affairs professionals to join its International Operations Regulatory Affairs team in Bangalore. This opportunity is designed for seasoned regulatory experts who want to work in a truly global environment, supporting product approvals, lifecycle management, and compliance across multiple international markets. If you have strong regulatory expertise, experience engaging with health authorities, and the ambition to contribute to high-quality, compliant product approvals, this role offers both impact and long-term career growth.

As a Regulatory Professional I at Novo Nordisk Global Business Services (GBS), you will operate at the intersection of global strategy and local regulatory execution. The position provides exposure to international submissions, cross-border stakeholder collaboration, and regulated market requirements, making it a high-value career move for professionals aiming to build authority in global regulatory affairs.

Company Overview

Novo Nordisk is a global healthcare company with more than 100 years of innovation in treating serious chronic diseases. The organization is globally recognized for its leadership in diabetes care, obesity management, and other chronic conditions, with products reaching millions of patients worldwide. Built on strong ethical foundations, scientific excellence, and patient-centric values, Novo Nordisk consistently ranks among the most trusted pharmaceutical companies globally.

Novo Nordisk Global Business Services (GBS) in Bangalore plays a critical role in supporting global operations through specialized capabilities in regulatory affairs, pharmacovigilance, clinical operations, and compliance. The Bangalore hub functions as an extension of global regulatory organizations based in Zurich and Copenhagen, ensuring fast, high-quality regulatory outcomes across International Operations.

Job Role & Responsibilities

The Regulatory Professional I role is positioned within International Operations Regulatory Affairs (IORA), supporting regulatory activities for new product registrations and post-approval lifecycle management across assigned countries.

Key Responsibilities

• Secure regulatory approvals for new products, including New Drug Applications (NDA) and Lifecycle Management (LCM) licenses, within defined timelines
• Manage end-to-end product lifecycle activities such as preparation, review, and submission of regulatory dossiers
• Prepare and review application forms in line with country-specific health authority requirements
• Engage directly with distributors, affiliates, and health authorities to ensure regulatory compliance and timely approvals
• Review and manage regulatory documentation for tenders and special submissions
• Maintain accurate and up-to-date regulatory information in Veeva Vault, including product dossiers and approval statuses
• Collaborate with affiliates on labelling development, review of promotional materials, and alignment with local regulatory legislation
• Monitor evolving regulatory landscapes and assess impact on product registrations and compliance strategies
• Provide regulatory support for post-approval changes, safety-related signals, and country-specific regulatory requirements

This role requires a high level of regulatory judgment, strong documentation skills, and the ability to operate independently in a complex international regulatory environment.

Eligibility / Qualifications

Novo Nordisk is seeking regulatory professionals with proven industry experience and strong exposure to international regulatory operations.

Educational Qualification

Post-Graduation or equivalent degree in a science discipline

Required Education Background

M.Pharm, M.Sc (Pharmaceutical Sciences, Life Sciences, Biotechnology, Regulatory Science), Pharm.D, or equivalent postgraduate science qualifications

Experience Requirements

• Minimum 5+ years of experience in pharmaceutical Regulatory Affairs
• At least 3 years of experience working with international stakeholders and decision-makers outside India
• Proven exposure to affiliate-based regulatory operations and shared service models
• Experience handling direct interactions and communications with health authorities
• Strong understanding of regulatory submissions, lifecycle management, and compliance requirements

Skill Requirements

• Working knowledge of global regulatory frameworks and country-specific HA expectations
• Hands-on experience with regulatory systems such as Veeva Vault
• Basic project management capabilities with the ability to manage multiple priorities
• Strong communication and stakeholder management skills
• High attention to detail and documentation accuracy

Location & Salary

• Job Location: Bangalore, Karnataka, India
• Work Location: Novo Nordisk Global Business Services (GBS), Bangalore
• Salary: Competitive and aligned with global pharmaceutical industry standards, based on experience and role scope

Novo Nordisk offers structured career growth, exposure to international regulatory projects, and a professional environment aligned with global compliance and quality expectations.

About the Department – International Operations Regulatory Affairs

International Operations Regulatory Affairs – Bangalore (IORA Bangalore) serves as a strategic extension of Novo Nordisk’s global IOSO Regulatory Affairs organization based in Zurich and Copenhagen. The team supports fast growth, portfolio integration, and regulatory continuity across international markets.

The department consists of highly skilled regulatory professionals delivering core regulatory capabilities, enabling efficient and compliant product approvals. By centralizing expertise in Bangalore, Novo Nordisk strengthens its ability to scale regulatory operations while maintaining high quality and compliance standards.

Working at Novo Nordisk

Working at Novo Nordisk means being part of a purpose-driven organization committed to defeating serious chronic diseases. The company fosters a culture of curiosity, accountability, and collaboration, encouraging employees to challenge conventional thinking and deliver sustainable healthcare solutions.

Employees at Novo Nordisk benefit from a strong ethical framework, inclusive workplace culture, and long-term career development opportunities. The organization values diversity, equality, and mutual respect, creating an environment where professionals can contribute meaningfully while growing their expertise.

Application Process

Interested candidates must apply online through the official Novo Nordisk careers portal. Link here

• Application Method: Online application only
• Required Document: Updated CV
• Application Deadline: 4 February 2026

Candidates should ensure their CV highlights regulatory submissions experience, international stakeholder engagement, and exposure to health authority interactions.

Important Disclaimer

Novo Nordisk has reported instances of fraudulent job offers made in its name. Applicants are advised that Novo Nordisk does not make unsolicited employment offers, does not charge recruitment fees, and does not request payments or equipment purchases during the hiring process. Always apply through official channels.

Frequently Asked Questions (FAQs)

Who is eligible to apply for the Regulatory Professional I role?

Postgraduate science professionals with over 5 years of Regulatory Affairs experience in the pharmaceutical industry.

Is international regulatory experience mandatory?

Yes. Experience working with international stakeholders and global affiliates is required.

Is this a pharmacovigilance role?

No. This role is focused on Regulatory Affairs within International Operations.

What systems knowledge is required?

Experience with regulatory systems such as Veeva Vault is preferred.

What is the application deadline?

The last date to apply is 4 February 2026.

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Company	Novo Nordisk
Vacancies	Regulatory Professional I
Required Education	Post-Graduation in Science (M.Pharm, M.Sc, Pharm.D or equivalent)
Experience	5+ Years

Tagged as: Pharma Jobs in Bangalore