Novo Nordisk Hiring Regulatory Professional I/II
Are you seeking Novo Nordisk Careers Bangalore or Pharmaceutical Regulatory Affairs Jobs in India? Global healthcare innovator Novo Nordisk Global Business Services (GBS) is recruiting experienced regulatory specialists for the role of Regulatory Professional I / II (Level 6) based in Bangalore.
This global registration and dossier management opening is ideal for science postgraduates (M.Pharm, Pharm.D, M.Sc, PhD) with over 5 years of regulatory experience in the pharmaceutical sector. Candidates must possess hands-on expertise compiling dossiers (eCTD, NeeS, ACTD formats) and working with Veeva Vault RA systems. To draft a resume detailing your international affiliate submissions or registration lifecycle metrics, read our guidelines on how to apply for healthcare and pharma jobs online.
📋 Job Details
| Particular | Details |
|---|---|
| Company | Novo Nordisk Global Business Services (GBS) |
| Position | Regulatory Professional I / II (Level 6) |
| Department | International Operations Regulatory Affairs (IORA) |
| Job Location | Bangalore, Karnataka, India |
| Employment Type | Full-Time |
| Experience Required | 5+ Years (with 3+ years working with international stakeholders) |
| Qualifications | Postgraduate Degree in Science (M.Pharm, Pharm.D, M.Sc, or equivalent) |
| Application Deadline | 20 July 2026 |
| Expected Salary | ₹12,00,000 – ₹20,00,000 per annum (Estimated) |
💼 Key Responsibilities
- Dossier Compilation: Build, compile, and format registration and re-registration dossiers in national, eCTD, NeeS, and ACTD formats.
- Lifecycle Management (LCM): Drive timely submissions of NDA applications and maintain post-approval compliance across international markets.
- System Maintenance: Ensure product records, dossier components, and approval timelines are accurately logged inside Veeva Vault.
- Stakeholder Interaction: Act as the primary regulatory point of contact for global affiliates, local distributors, and Health Authorities.
- Labelling & Promotion: Collaborate with affiliates to develop product labelling, and review and approve promotional materials.
- Regulatory Intelligence: Support affiliates in monitoring local country regulatory developments and ensuring compliance with internal SOPs.
To learn how global regulatory affairs salaries compare to conventional pharmacovigilance drug safety associate and clinical data programming structures, read our report on Pharmacovigilance Salary: India vs USA.
🎓 Required Qualifications & Skills
- Education: Postgraduate degree in Science (M.Pharm, Pharm.D, M.Sc) in Regulatory Affairs, Biotechnology, Microbiology, or related fields.
- Core Experience: Minimum 5 years of pharmaceutical industry experience in Regulatory Affairs with 3+ years managing cross-functional projects outside India.
- Format Expertise: Hands-on experience compiling dossiers using standard global templates (ACTD, eCTD, NeeS).
- Software Knowledge: In-depth familiarity with electronic submission tools and Veeva Vault RA environments.
- Communication: High level of English proficiency (written and spoken) to manage complex stakeholder communications.
For science postgraduates evaluating regulatory affairs pathways compared to conventional laboratory quality control or direct formulation roles, read our analysis on B.Pharm Careers after Graduation: India vs USA.
🎁 Why Join Novo Nordisk?
- Work with a leading global healthcare company with more than 100 years of clinical innovation.
- Gain exposure to international drug submissions, health authority guidelines, and multi-country portfolios.
- Collaborative International Operations (IORA) team structure with Swiss and Danish affiliates.
- Modern work environment utilizing leading digital platforms like Veeva Vault.
To review your basic knowledge of clinical terminology, safety registries, and GCP standards before your technical panel interviews, try our interactive Clinical Trial Assistant (CTA) Quiz.
💡 Regulatory Professional vs Healthcare IT
Regulatory Professionals compile registration dossiers, manage product licenses, and audit Veeva database entries, whereas Healthcare IT professionals support software deployments. To explore these differences, read our comparison on Healthcare IT vs Clinical Healthcare.
📝 Resume Tips for Novo Nordisk Candidates
- Highlight Global Stakeholders: Specify which regions (e.g., EU, LATAM, APAC, Middle East) you have directly compiled dossiers for.
- Detail Veeva Experience: Emphasize your hands-on experience using Veeva Vault or other RIM (Regulatory Information Management) platforms.
- Specify Submission Formats: List eCTD, NeeS, or ACTD compilation tools and software versions you are proficient with.
💬 Novo Nordisk Regulatory Professional Interview Questions
- Q1. What is the difference between eCTD and NeeS dossier formats?
Answer Guidance: eCTD (Electronic Common Technical Document) is XML-based, utilizing backbone index files for automated navigation, lifecycle tracking, and validation. NeeS (Non-eCTD Electronic Submission) is a folder-based structure with PDF files and electronic tables of contents but without the XML backbone. - Q2. How do you manage a situation where an affiliate requests dossier variations that conflict with core guidelines?
Answer Guidance: I review local country legislation, consult IORA database files to check if similar variations have been approved in adjacent regions, and schedule a alignment call with the affiliate to discuss compliant alternatives. - Q3. Explain the importance of lifecycle management (LCM) in pharmaceutical regulatory affairs.
Answer Guidance: LCM ensures that post-approval modifications—such as manufacturing site transfers, packaging updates, variations, and renewals—are compiled, submitted, and approved on time to ensure product supply continuity.
🚀 How to Apply?
Interested and eligible candidates can submit their applications directly via Novo Nordisk's official careers board. Click the button below to apply:
Apply Online – Novo Nordisk Career Board❓ Frequently Asked Questions
Q. What is the required experience for the Regulatory Professional I/II opening?
Novo Nordisk requires a minimum of 5 years of pharmaceutical regulatory affairs experience, with at least 3 years working with global stakeholders.
Q. Do I need experience with Veeva Vault to apply?
Veeva Vault experience is highly preferred as it is the primary regulatory database system used by the team.
Q. What is the application deadline for this position?
The application window closes on 20 July 2026.
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