Regulatory Professional – Novo Nordisk

The Regulatory Professional Job at Novo Nordisk offers an outstanding opportunity for life sciences and pharmaceutical compliance experts to make a global impact. Novo Nordisk Global Business Services (GBS) is looking for talented professionals to join their International Operations Regulatory Affairs team in Bangalore. In this comprehensive job board post, we break down everything you need to know about this career opening, including key roles, required skills, and estimated salaries.

Overview of the Role

As a vital member of the International Operations team, the successful candidate will secure crucial regulatory approvals that pave the way for life-changing therapies to enter international markets. This is a Level 6 position designed to manage the end-to-end drug product lifecycle, covering both new drug applications (NDA) and ongoing lifecycle management (LCM) licenses.

Working at Novo Nordisk means being part of a legacy that successfully combats serious chronic diseases worldwide. The Bangalore GBS site operates as a seamless expansion of global corporate hubs in Zurich and Copenhagen, establishing a high-performance environment where your individual drive translates directly into better patient outcomes and cross-functional business continuity.

Responsibilities

1. Application Submission: Lead the compilation and timely submission of registration applications in strict alignment with regional Health Authority (HA) guidelines.

2. Stakeholder Engagement: Act as a reliable liaison for local distributors, health authorities, and affiliate teams to expedite approvals and handle tender document reviews.

3. Data Management: Utilize industry-standard tools like Veeva Vault RA systems to keep product dossiers and authorization documents securely archived and updated.

4. Labelling & Compliance: Support cross-functional affiliates in reviewing promotional materials, local packaging compliance, and product specimen labeling.

Also Check: Patent Coordinator – Novo Nordisk

Qualifications

1. Education: Post-Graduation or equivalent professional degree in Life Sciences, Pharmacy, or a related scientific discipline.

2. Experience: A minimum of 5 years of domain experience within the pharmaceutical industry, specifically focused on Regulatory Affairs.

3. Global Exposure: At least 3+ years of experience collaborating with cross-functional stakeholders and decision-makers outside India across diverse time zones.

4. Technical Skills: Robust proficiency with standard technical registration formats (eCTD, NeeS, ACTD) and electronic management workflows.