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Would you like to be part of an area where we bring treatments to patients? Do you want to lead a skilled team and to set direction and pace of ambitious initiatives in the organisation? If you want to be part of a company with a high focus on work life balance, apply now for this life-changing career opportunity! You might be our new Associate Director in one of the Regulatory Affairs CMC & Devices departments in Søborg, Denmark.
The position
As an Associate Director in Regulatory Affairs CMC & Device, you will lead a dedicated team of experienced RA Professionals and play a pivotal role in shaping and influencing regulatory strategies and getting Novo Nordisk products to market.

Your main responsibilities will be focused on:

People management and development

Prioritising and forecasting resource allocation

Driving regulatory strategies on innovative products together with Regulatory Leads in the department

Effectively communicating our regulatory messages to relevant stakeholders

Drive improvement initiatives within the department and across the RA CMC & Device area

Qualifications
To be a competitive candidate, you should have:

A master’s degree related to Life Sciences and experience working with pharmaceuticals, devices, or combination products

At least five years of proven track record experience working in a large organization and/or health authorities w...