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Regulatory Professional Ii

Novo Nordisk
6+ years
INR 18 LPA – 25 LPA
Bangalore, India
1 June 12, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Communication Skills, CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes

Regulatory Professional II

Company: Novo Nordisk
Role: Regulatory Professional II
Department: Regulatory Affairs & Safety Pharmacovigilance (RA-CMC)
Location: Bangalore
Employment Type: Full Time
Experience Required: 6+ Years
Education: Graduate/Postgraduate in Life Sciences, Pharmacy, Chemistry, Medicine, Biotechnology, or related fields


About the Role

Novo Nordisk is seeking an experienced Regulatory Affairs professional to support global regulatory submissions, Life Cycle Management (LCM), and RA-CMC activities. The role focuses on ensuring timely approvals and maintaining regulatory compliance for products across regulated and emerging markets.

The selected candidate will work closely with global stakeholders, health authorities, and affiliate teams to support product registrations, post-approval changes, renewals, and regulatory strategy development.


Key Responsibilities

  • Support global regulatory submission planning and execution.

  • Develop and maintain Regulatory Submission Plans.

  • Contribute to regulatory strategy development using regulatory intelligence.

  • Manage Change Requests, Deviations, and Health Authority responses.

  • Support NDA rollouts, renewals, annual reports, and post-approval changes.

  • Maintain and update marketing authorizations globally.

  • Work extensively with Veeva Vault Submissions & Registrations.

  • Ensure regulatory documentation meets global compliance requirements.

  • Collaborate with affiliate and global regulatory teams.

  • Manage stakeholder communications across multiple regions and time zones.

  • Support Life Cycle Management (LCM) activities for commercial products.


Required Skills

  • Regulatory Affairs (RA)

  • RA-CMC (Chemistry, Manufacturing & Controls)

  • Life Cycle Management (LCM)

  • Regulatory Strategy Development

  • Health Authority Interactions

  • Post-Approval Changes

  • NDA Submission Support

  • Veeva Vault RIM

  • Regulatory Intelligence

  • Stakeholder Management

  • Project Management

  • Global Regulatory Compliance


Preferred Experience

  • Experience with regulated and emerging markets.

  • Exposure to China and Japan regulatory submissions.

  • Experience in both affiliate and global regulatory environments.

  • Knowledge of multiple dosage forms.

  • Strong understanding of pharmaceutical product lifecycle management.

  • Experience working with Veeva Vault Submission and Registration modules.


Ideal Candidate Profile

  • 6–10 years of Regulatory Affairs experience.

  • Strong RA-CMC background.

  • Ability to manage multiple submissions simultaneously.

  • Excellent communication and negotiation skills.

  • Comfortable working with global cross-functional teams.

  • Proactive and highly organized professional.