Department – Regulatory Quality & Clinical reporting
Location – Bangalore
Shape how Novo Nordisk brings life-changing medicines to patients worldwide – by leading the team that ensures every regulatory submission meets the highest standards of quality and compliance.
Your current role
As Associate Director in Publishing, you will lead a team responsible for global publishing activities. You will hold Novo Nordisk's eCTD expertise and have decision authority over submission structure for health authorities. You will be leading the area in accordance with the area strategy and company transformation.
Your Key Responsibilities Will Include
Leading and developing your team in line with the Novo Nordisk Way – clarifying direction, coaching talent, coordinating priorities and ensuring optimal resource utilisation across publishing deliverables
Driving business performance by setting clear targets, optimising team output and maintaining focus on key deliverables within deadlines
Owning quality,
compliance and environmental management for the team – establishing and maintaining the local QMS in compliance with the Novo Nordisk Quality Manual
Managing complex stakeholder relationships across Regulatory Affairs, Clinical Reporting, R&D;, Global Safety, QA, DD⁢ and senior management, as well as external health authorities, industry peers and IT vendors
Working in the leadership team in making clear strategic direction for the area
Representing Novo Nordisk in industry fora such as the EFPIA eCTD subgroup, Veeva eCTD community and RegOps Symposium – contributing to the evolution of eCTD standards globally
Your new department
In Research & Development, you'll be part of a unit that explores bold scientific ideas and advances them into clinical testing. We combine curiosity, AI tools, and human data to develop transformative therapies. Through collaboration and operational excellence, we shape and deliver an innovative pipeli
📌 Assoc Director (Bengaluru)
🏢 Novo Nordisk
📍 Bengaluru
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