Manager in Global Technical Operations
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Hillerød
Do you want to lead a team that excels at ramping up new processes, driving continuous improvement? Would you like to use your leadership and manufacturing expertise to shape how the team ensures the transition of new lines from projects to reliable production lines installed at our Contract Manufacturing Organisations (CMOs)?If so, this is an opportunity to join our Global Contract Manufacturing Devices (GCM Devices) department for Assembly and Pack, where we support our sub-contractors from the lines are delivered until they are decommissioned. Apply today! The Position
As Manager, you lead a team that takes the responsibility for and support stable deliveries from our new assembly & packaging lines. The assets are located at our global CMOs across Europe, Asia and USA. You will be playing a pivotal role in how we shape our ongoing and future expansions across a fast-growing network. For lines in the project stage your team participates or drives factory and site acceptance tests and performance qualification. For lines in operation your team plays a key role during the ramp up phase before they support the normal continues improvement track together with the supplier. Your role will be to ensure we always have the right team, formation and structures to ensure we drive an efficient network that delivers according to our commitments. Additionally, you ensure seamless collaboration between your team, your colleague in a similar position, our device design organization, and global contract manufacturing partners.Your key activities include: Managing and mentoring a team of experts to support global contract manufacturing operations, with a focus on ramping up initiatives and new device introductions
Developing and implementing strategies to optimize collaboration and performance
Overseeing the coordination of activities between internal teams and external contract manufacturing partners for new device introductions
Ensuring compliance with industry regulations and quality standards in all aspects of the manufacturing process related to setting up and running our equipment at CMOs
Collaborating with cross-functional teams to drive continuous improvement in manufacturing processes and outcomes
Providing leadership and mentorship to team members, fostering a culture of growth and development
Furthermore, you coordinate the hiring of the future supporters and experts to keep up with our expanding network. Qualifications
To be successful in this role, we believe you: Hold a minimum of a bachelor’s degree in a relevant field, coupled with proven experience in managing teams and ramping up support in a manufacturing or related industry
Demonstrate in-depth understanding of global contract manufacturing processes and best practices, particularly related to new device introductions
Showcase strong leadership and communication skills with a track record of building and developing high-performing teams
Have knowledge of industry regulations and quality standards related to new device introductions
Display proficiency in both spoken and written English
On a personal level, you excel in collaborating with cross-functional teams and external partners, fostering smooth cooperation and building strong partnership. You are not afraid to make decisions and set clear directions, engaging and motivating your team to drive successful results. You value diverse opinions and maintain a curious, open mindset, enabling you to thrive in a global setting with many stakeholders involved, all while tackling challenges boldly. About the Department
GCM Devices is a newly established functional area in Novo Nordisk that consists of around 200 people. We are responsible for all external production of pen needles, components and sub-assemblies for ’s pen systems, as well as for the license to operate and technical support to our CMO for device assembly and packaging.From this department, we manage a network of more than 25 contract manufacturers in Asia, Europe, and the Americas, and the expected growth of ’s new drug products is driving the need for more further expansions at existing and new contract manufacturers to reach more patients.You will become part of a truly international team, where colleagues are eager to exchange knowledge, as well as gain insights from your expertise. Within our team, we foster open communication, a positive mindset, and a strong enthusiasm for both personal and professional growth. Working at
We are a proud life-science company, and life is our reason to exist. We’re inspired by life in all its forms and shapes, ups and downs, opportunities and challenges. For employees at , life means many things – from the building blocks of life that form the basis of ground-breaking scientific research, to our rich personal lives that motivate and energize us to perform our best at work. Ultimately, life is why we’re all here - to ensure that people can lead a life independent of chronic disease. Contact
If you have questions about the role, please reach out to Senior Manager Jesper Jensen at +. Deadline
23 August 2024.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 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.
As Manager, you lead a team that takes the responsibility for and support stable deliveries from our new assembly & packaging lines. The assets are located at our global CMOs across Europe, Asia and USA. You will be playing a pivotal role in how we shape our ongoing and future expansions across a fast-growing network. For lines in the project stage your team participates or drives factory and site acceptance tests and performance qualification. For lines in operation your team plays a key role during the ramp up phase before they support the normal continues improvement track together with the supplier. Your role will be to ensure we always have the right team, formation and structures to ensure we drive an efficient network that delivers according to our commitments. Additionally, you ensure seamless collaboration between your team, your colleague in a similar position, our device design organization, and global contract manufacturing partners.Your key activities include:
To be successful in this role, we believe you:
GCM Devices is a newly established functional area in Novo Nordisk that consists of around 200 people. We are responsible for all external production of pen needles, components and sub-assemblies for ’s pen systems, as well as for the license to operate and technical support to our CMO for device assembly and packaging.From this department, we manage a network of more than 25 contract manufacturers in Asia, Europe, and the Americas, and the expected growth of ’s new drug products is driving the need for more further expansions at existing and new contract manufacturers to reach more patients.You will become part of a truly international team, where colleagues are eager to exchange knowledge, as well as gain insights from your expertise. Within our team, we foster open communication, a positive mindset, and a strong enthusiasm for both personal and professional growth. Working at
We are a proud life-science company, and life is our reason to exist. We’re inspired by life in all its forms and shapes, ups and downs, opportunities and challenges. For employees at , life means many things – from the building blocks of life that form the basis of ground-breaking scientific research, to our rich personal lives that motivate and energize us to perform our best at work. Ultimately, life is why we’re all here - to ensure that people can lead a life independent of chronic disease. Contact
If you have questions about the role, please reach out to Senior Manager Jesper Jensen at +. Deadline
23 August 2024.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 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 "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Hillerød.
Jobbet er oprettet på vores service den 12.8.2024, 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.
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Statistik over udbudte øvrige i Hillerød over tid
| Dato | Alle jobs som øvrige |
|---|---|
| 15. september 2024 | 85 |
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| 13. september 2024 | 80 |
| 12. september 2024 | 68 |
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| 4. september 2024 | 64 |
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| 31. august 2024 | 70 |
| 30. august 2024 | 71 |
| 29. august 2024 | 68 |
| 28. august 2024 | 70 |
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| 25. august 2024 | 75 |
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| 22. august 2024 | 75 |
| 21. august 2024 | 72 |
| 20. august 2024 | 70 |
| 19. august 2024 | 61 |
| 18. august 2024 | 69 |
| 17. august 2024 | 68 |
| 16. august 2024 | 67 |