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Do you enjoy working across the value chain to find cross-functional solutions, creating transparency and optimisation of processes? Are you excited to encourage innovation and see the tangible outcome of it? Do you get motivated working with regulations, processes, data, and people?
If you want to be a part of enabling and supporting the growing portfolio of products and life cycle management activities in Novo Nordisk, then don’t miss this opportunity. Apply now and join our journey as Project Manager!
The position
As Project Manager, you will drive projects that enable us to manage and handle regulatory activities across the project portfolio – joining Global Regulatory Affairs on the digitalisation journey.
You will be joining a relatively new department that is in the process of establishing new work processes for handling regulatory approvals and activities primarily related to manufacturing capacity expansion. The atmosphere in the team is informal and good humour is always welcome.
Your main responsibilities would include:
You will be joined by an increased numbers of colleagues in the department. The work environment is flexible and very open minded. You will have the opportunity for flexible working conditions such as working from home.
Qualifications
To be successful in this role, you need to have M.Sc. or similar university degree and minimum 5 years of end-to-end experience with complex cross-organizational process optimisation projects.
Additionally, you need to have the following:
As a person, you are eager to learn, well organised, and a proactive problem solver. You enjoy working in a project-oriented organization with a diverse and global team. Finally, you focus on moving projects forward proactively, can work independently, and bring an innovative mindset in search of novel solutions to the challenges we face.
About the department
You will be part of a new department, which is anchored with Regulatory Affairs (RA) CMC (Chemistry, Manufacturing and Controls) & Device in Global Regulatory Affairs. The department will be overall responsible for maintaining regulatory overview of ongoing applications and coordinate regulatory submissions arising from new facilities, product transfers and changes in manufacturing processes.
One of the departments main target and responsibility is to drive new processes, to facilitate faster approvals and more transparency and better planning of ongoing applications. An unprecedented number of global regulatory approvals will be needed due to the ongoing capacity investments in production as well as a continued need for increased regulatory flexibility in the supply network, which the department will be responsible for supporting.
The department is part of RA CMC & Device and is supporting regulatory activities in both development projects as well as on our marketed products. The area is around 130 colleagues and works closely with the RA CMC & Device unit in GBS, Bangalore, as well as the regulatory colleagues in our affiliate offices.
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 Department Director, Malene Østergaard Jørgensen at + 45 3079 5844.
Deadline
13 November 2022. Applications will be reviewed continuously, and we will begin conducting interviews already during the posting period, so please do not hesitate to apply.
You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. 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
If you want to be a part of enabling and supporting the growing portfolio of products and life cycle management activities in Novo Nordisk, then don’t miss this opportunity. Apply now and join our journey as Project Manager!
The position
As Project Manager, you will drive projects that enable us to manage and handle regulatory activities across the project portfolio – joining Global Regulatory Affairs on the digitalisation journey.
You will be joining a relatively new department that is in the process of establishing new work processes for handling regulatory approvals and activities primarily related to manufacturing capacity expansion. The atmosphere in the team is informal and good humour is always welcome.
Your main responsibilities would include:
- Driving the development of processes and a new supporting system to keep track of and monitor requirements, as well as to enable the creation of data intelligence into business processes
- Collaborating with stakeholders across Global Regulatory Affairs, International Operations and Regulatory Affairs internal ART team (Agile Release Team), as they have the responsibility for IT implementation
- Coordinating activities for specific project execution within the area's scope
- Managing deadlines in a complex international communication context that spans time zones, cultures, and circumstances
You will be joined by an increased numbers of colleagues in the department. The work environment is flexible and very open minded. You will have the opportunity for flexible working conditions such as working from home.
Qualifications
To be successful in this role, you need to have M.Sc. or similar university degree and minimum 5 years of end-to-end experience with complex cross-organizational process optimisation projects.
Additionally, you need to have the following:
- Experience from the pharmaceutical industry will be valued, however specific practical experience and project management toolbox will be weighted higher
- Strong cross value chain business understanding
- Good stakeholder management skills at all levels
- Translating strategies into tactical responses via operational solutions in processes, information technology solutions, and organizational implementation
- High proficiency in English
As a person, you are eager to learn, well organised, and a proactive problem solver. You enjoy working in a project-oriented organization with a diverse and global team. Finally, you focus on moving projects forward proactively, can work independently, and bring an innovative mindset in search of novel solutions to the challenges we face.
About the department
You will be part of a new department, which is anchored with Regulatory Affairs (RA) CMC (Chemistry, Manufacturing and Controls) & Device in Global Regulatory Affairs. The department will be overall responsible for maintaining regulatory overview of ongoing applications and coordinate regulatory submissions arising from new facilities, product transfers and changes in manufacturing processes.
One of the departments main target and responsibility is to drive new processes, to facilitate faster approvals and more transparency and better planning of ongoing applications. An unprecedented number of global regulatory approvals will be needed due to the ongoing capacity investments in production as well as a continued need for increased regulatory flexibility in the supply network, which the department will be responsible for supporting.
The department is part of RA CMC & Device and is supporting regulatory activities in both development projects as well as on our marketed products. The area is around 130 colleagues and works closely with the RA CMC & Device unit in GBS, Bangalore, as well as the regulatory colleagues in our affiliate offices.
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 Department Director, Malene Østergaard Jørgensen at + 45 3079 5844.
Deadline
13 November 2022. Applications will be reviewed continuously, and we will begin conducting interviews already during the posting period, so please do not hesitate to apply.
You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. 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 28.10.2022, 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
Herunder ser du udviklingen i udbudte øvrige i Søborg over tid. Bemærk at jobs der ikke har en bestemt geografi ikke er medtaget i tabellen. I den første kolonne ser du datoen. I den næste kolonne ser du det samlede antal øvrige.
Se flere statistikker her:
Statistik over udbudte øvrige i Søborg over tid
| Dato | Alle jobs som øvrige |
|---|---|
| 4. oktober 2024 | 66 |
| 3. oktober 2024 | 65 |
| 2. oktober 2024 | 64 |
| 1. oktober 2024 | 63 |
| 30. september 2024 | 67 |
| 29. september 2024 | 62 |
| 28. september 2024 | 62 |
| 27. september 2024 | 61 |
| 26. september 2024 | 58 |
| 25. september 2024 | 54 |
| 24. september 2024 | 53 |
| 23. september 2024 | 53 |
| 22. september 2024 | 56 |
| 21. september 2024 | 56 |
| 20. september 2024 | 55 |
| 19. september 2024 | 56 |
| 18. september 2024 | 55 |
| 17. september 2024 | 58 |
| 16. september 2024 | 57 |
| 15. september 2024 | 60 |
| 14. september 2024 | 60 |
| 13. september 2024 | 60 |
| 12. september 2024 | 56 |
| 11. september 2024 | 57 |
| 10. september 2024 | 57 |
| 9. september 2024 | 56 |
| 8. september 2024 | 56 |
| 7. september 2024 | 56 |
| 6. september 2024 | 58 |
| 5. september 2024 | 60 |
| 4. september 2024 | 61 |