Øvrige i Søborg
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Do want to be a part of enabling and supporting the growing portfolio of products and life cycle management activities in Novo Nordisk? Would you like to join our business transformation journey in Regulatory Affairs (RA)? Then, this is your moment. Start your application for a life-changing career!
The position
As a Senior Regulatory Professional, you will drive activities that enable us to manage and handle regulatory activities across the product portfolio, with a primary focus on securing a smooth and effective integration of new acquisitions into our Submission & Registration process in Vault RIM. Your main role will be to plan, drive and facilitate processes and projects to enable Regulatory Affairs (RA) to work with new products in Vault RIM.
Your main responsibilities will be:
Qualifications
The ideal candidate has:
On a personal level you are:
About the department
You will have the unique opportunity to be part of a strategically crucial business transformation across multiple processes and geographies and take active part in shaping the way RA will work in the future. You will join the RA Business Transformation department that plays a key role to support and enable this transformation.
Global Regulatory Affairs is an exciting area involved across the full value chain. We are responsible for global regulatory strategies to obtain and maintain regulatory licenses for current and future products, responsive to the worldwide business needs of Novo Nordisk.
You will work in a fast-paced environment where it is important to be able to manage deadlines in a complex context of international communication across time zones, cultures, and circumstances. The atmosphere in the team is informal and good humour is always welcome.
Working at Novo Nordisk
At Novo Nordisk, 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 embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales.
Contact
For further information please contact Sana Moussa + 45 3079 2488.
Deadline
13 November 2022.
Please be aware that only candidates who also submit a cover letter will be taken into consideration for the position.
Applications will be reviewed continuously, and we will begin conducting interviews already during the posting period, so please do not hesitate to apply.
To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV.
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
At Novo Nordisk 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.
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The position
As a Senior Regulatory Professional, you will drive activities that enable us to manage and handle regulatory activities across the product portfolio, with a primary focus on securing a smooth and effective integration of new acquisitions into our Submission & Registration process in Vault RIM. Your main role will be to plan, drive and facilitate processes and projects to enable Regulatory Affairs (RA) to work with new products in Vault RIM.
Your main responsibilities will be:
- Drive and implement integration of new products in our internal submission and registration process in Vault RIM, in close collaboration with stakeholders across Research & Development and the Data, Digital & IT organisation
- Drive and implement continuous improvements to our submission and registration processes in Vault RIM
- Manage and coordinate specific projects within the responsibility of the area
Qualifications
The ideal candidate has:
- A M.Sc. in a relevant field, such as science, pharmacy, or equivalent is required
- Minimum 5 years of experience from the pharmaceutical industry and regulatory affairs. A strong cross-value chain business understanding, good stakeholder management capabilities and communication skills
- Project Management background and experience
- Experience working with Vault RIM Submission and Registration is required
- Experience with agile Project Management and Scaled Agile Framework (SAFe) is an advantage
- High proficiency in English
On a personal level you are:
- Curious to learn, well organised and a proactive problem solver
- Enjoying working in a diverse and global team and in a project-oriented organisation
- Thriving in an environment with changing circumstances and have a can-do attitude as well as a healthy sense of humour
- Focus on jointly moving the projects, can work independently and bring an innovative mindset seeking novel solutions to the challenges we face
About the department
You will have the unique opportunity to be part of a strategically crucial business transformation across multiple processes and geographies and take active part in shaping the way RA will work in the future. You will join the RA Business Transformation department that plays a key role to support and enable this transformation.
Global Regulatory Affairs is an exciting area involved across the full value chain. We are responsible for global regulatory strategies to obtain and maintain regulatory licenses for current and future products, responsive to the worldwide business needs of Novo Nordisk.
You will work in a fast-paced environment where it is important to be able to manage deadlines in a complex context of international communication across time zones, cultures, and circumstances. The atmosphere in the team is informal and good humour is always welcome.
Working at Novo Nordisk
At Novo Nordisk, 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 embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales.
Contact
For further information please contact Sana Moussa + 45 3079 2488.
Deadline
13 November 2022.
Please be aware that only candidates who also submit a cover letter will be taken into consideration for the position.
Applications will be reviewed continuously, and we will begin conducting interviews already during the posting period, so please do not hesitate to apply.
To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV.
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
At Novo Nordisk 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.
Print job Send to e-mail
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 14.10.2022, 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.
- Øvrige
- Søborg
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Statistik over udbudte jobs som øvrige i Søborg
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Statistik over udbudte øvrige i Søborg over tid
| Dato | Alle jobs som øvrige |
|---|---|
| 10. juli 2024 | 71 |
| 9. juli 2024 | 72 |
| 8. juli 2024 | 68 |
| 7. juli 2024 | 71 |
| 6. juli 2024 | 71 |
| 5. juli 2024 | 72 |
| 4. juli 2024 | 68 |
| 3. juli 2024 | 71 |
| 2. juli 2024 | 69 |
| 1. juli 2024 | 66 |
| 30. juni 2024 | 71 |
| 29. juni 2024 | 71 |
| 28. juni 2024 | 75 |
| 27. juni 2024 | 72 |
| 26. juni 2024 | 70 |
| 25. juni 2024 | 71 |
| 24. juni 2024 | 70 |
| 23. juni 2024 | 71 |
| 22. juni 2024 | 71 |
| 21. juni 2024 | 72 |
| 20. juni 2024 | 73 |
| 19. juni 2024 | 71 |
| 18. juni 2024 | 67 |
| 17. juni 2024 | 65 |
| 16. juni 2024 | 71 |
| 15. juni 2024 | 71 |
| 14. juni 2024 | 71 |
| 13. juni 2024 | 68 |
| 12. juni 2024 | 64 |
| 11. juni 2024 | 65 |
| 10. juni 2024 | 63 |