Associate Director for Regulatory Affairs Device
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Søborg
If you want to be part of an area where we have a high focus on work-life balance, development, and great career opportunities, then you could be what we are looking for. We are looking for a candidate to lead skilled employees in their daily work and set the direction and pace of ambitious initiatives in the organization. If this sounds like something that could suit you, you might be our new Associate Director in the Regulatory Affairs Devices Department at in Søborg - Apply now for this life-changing opportunity!
The position
As an Associate Director in the Regulatory Affairs Devices Department, you will lead a dedicated team of experienced RA Professionals and play a pivotal role in shaping and influencing regulatory strategies and getting products to market.
Your main responsibilities will be focused on: People management and development Driving regulatory strategies on innovative products Prioritizing and forecasting resource allocation Effectively communicating our regulatory messages to relevant stakeholders Qualifications
To be a competitive candidate, you should have: A master’s degree related to Life Sciences and experience working in combination products, devices and/or pharmaceuticals At least five years of demonstrated experience working in a large organization and/or health authorities within the regulatory affairs area Strong people management experience
On a personal level, you should be self-motivated and have a strategic mindset. You need to bring a proactive and innovative approach to provide valuable input and support, setting the strategic direction. Finally, you must be able to communicate complex topics to many different stakeholders and have a positive attitude.
About the department
The RA Devices Department is responsible for driving the RA strategy and submission activities for drug-device combination products and devices in development projects. We are responsible for planning and implementing regulatory strategies based on current regulations and negotiating with authorities to ensure minimum time to market.
Working at
At , we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We never shy away from opportunities to develop, we seize them. From research and development to manufacturing, marketing, and sales – we’re all working to move the needle on patient care.
Contact
For further information, please contact Thomas Wejs Møller - Senior Director - at
Deadline
1 April 2024 We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
The position
As an Associate Director in the Regulatory Affairs Devices Department, you will lead a dedicated team of experienced RA Professionals and play a pivotal role in shaping and influencing regulatory strategies and getting products to market.
Your main responsibilities will be focused on:
To be a competitive candidate, you should have:
On a personal level, you should be self-motivated and have a strategic mindset. You need to bring a proactive and innovative approach to provide valuable input and support, setting the strategic direction. Finally, you must be able to communicate complex topics to many different stakeholders and have a positive attitude.
About the department
The RA Devices Department is responsible for driving the RA strategy and submission activities for drug-device combination products and devices in development projects. We are responsible for planning and implementing regulatory strategies based on current regulations and negotiating with authorities to ensure minimum time to market.
Working at
At , we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We never shy away from opportunities to develop, we seize them. From research and development to manufacturing, marketing, and sales – we’re all working to move the needle on patient care.
Contact
For further information, please contact Thomas Wejs Møller - Senior Director - at
Deadline
1 April 2024 We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
Information og data
Denne ledige stilling har jobtypen "Apoteker", og befinder sig i kategorien "Sundhed og forskning".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 8.1.2024, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Apoteker
- Søborg
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| Dato | Alle jobs som apotekere |
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| 24. april 2024 | 6 |
| 23. april 2024 | 5 |
| 22. april 2024 | 8 |
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| 1. april 2024 | 15 |
| 31. marts 2024 | 17 |
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