Novo Nordisk is hiring B. Pharma/ M. Pharma for Regulatory Affairs – Apply Now

Attention B. Pharma/M. Pharma graduates! Novo Nordisk is on the lookout for skilled Regulatory Affairs Professionals – Labelling. Join us in shaping the future of pharmaceuticals while advancing your career. Explore this exciting opportunity to contribute your expertise and make a meaningful impact in the industry. Apply now to become part of our dynamic team at Novo Nordisk.

About the Department

The RA Labelling team in Global Business Services (GBS) Bangalore is part of the global RA hub, consisting of a strong team of high-caliber regulatory professionals and graphics designers. We offer core Regulatory Affairs (RA) competencies to enable Novo Nordisk (NN) to secure fast, high-quality product approvals. Our team provides strategic and operational support on a global scale across the value chain, working closely with colleagues in RAHQ, Denmark, and affiliates worldwide.

Qualification & Experience

• Master’s degree in science/pharmacy/medicine with 3-4 years of relevant experience or Bachelor’s degree with 5-7 years of experience.
• Fluent in written and spoken English.
• Proficiency in label development, health authority interactions, and regulatory intelligence.
• Strong project management skills and understanding of business management principles.
• Knowledge of R&D value chain, digital health, competitive intelligence, pharmacovigilance, clinical pharmacology, market access, and real-world evidence generation preferred.

Job Description

Are you detail-oriented and passionate about ensuring regulatory compliance? Do you thrive in a fast-paced and global environment? We are looking for a Regulatory Professional I – Labelling to join our team in Global Business Services (GBS) Bangalore. If you are ready for a challenging role where you can make a difference, read on and apply today for a life-changing career.

Roles and Responsibilities

• Packaging Material Coordination: Collaborate with stakeholders across Regulatory Affairs, Affiliate, Product Supply, and Marketing to plan and coordinate packaging material for global markets.
• Labelling Request Management: Assess and align expectations for new or updated packaging materials, ensuring prerequisites are met for execution. Collaborate with RA and Product Supply for planning and execution.
• Launch Coordination: Plan and track medium complexity labelling launches using relevant tools and systems, involving stakeholders from RA, Affiliates, and Product Supply.
• Compliance Assurance: Maintain training according to internal and external requirements, ensuring adherence to current good manufacturing practices (GMP) and Novo Nordisk procedures in daily work.
• Departmental Engagement: Actively participate in meetings, contribute to continuous improvement initiatives, and engage in projects to drive positive change within the department and across the organization.

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