Global Inspection Project Manager
Bagsværd
Are you ready to support and be part of shaping the future of manufacturing in ? Are you motivated by standardization and scaling up? Are you ready to change the game together with your team and the production sites around the world?
Then this is a unique opportunity to become part of a team of highly competent professionals and specialist impacting the way we produce diabetes products around the world. Join us and become our new Global Inspection Project Manager! About the department We are a newly established organisational unit, Aseptic Manufacturing Engineering (AME). With almost 100 colleagues, we play a key role in accelerating a major transformation to improve performance across a global network of factories in Asia, Europe as well as North and South America to meet the need of the increasing number of people living with diabetes and obesity. AME is an organizational unit in Aseptic Manufacturing (AM), which is the largest production area in . With more than 5,000 employees, AM is a truly global organization responsible for producing products for launches of all new diabetes and obesity products in supplying nearly 50% of the world’ insulin (for more information please visit Come join us in driving change for patients around the world. The position
As our new Global Inspection Project Manager, you will have the responsibility and ownership of the new fleet of Inspection lines, with focus on maintaining the standardized equipment through development and implementation in line with the global standards and asset management strategy for global Injectable Finished Products (IFP). You will report directly to the Director of the Standardized Inspection Lines Program and be part of the new department. As such, you will be able maintain a key role in establishing the set of standards and maximizing performance for the inspection line fleet for the future.
Your key responsibilities will include: Develop, implement, and sustain a standardized approach for the inspection track
Ensure developed Vision/Inspection solutions remain standard
Support key validation activities for Vision/Inspection Collaborate with Inspection Process Group and Process Manager
Provide direction for new inspection lines, including assessing improvements and process optimizations for Vision performance
You can also look forward to tasks, like optimizing shutdowns, creating standard recipes, coordinating global and local resources, and following equipment changes with site partners.
The lines will be located at existing IFP sites, with experience and knowledge of earlier generation lines. Thus, some travel is to be expected (less than 20%) along with supporting sites during office hours for the given site.
Qualifications
To succeed in this role, you have: An academic degree in engineering or a related technical field
Technical field experience in a global context, including international assignments
Profound project management knowledge and experience being part of global teams
Broad hands-on experience in engineering and Vision and automation, with a track record in driving equipment improvements
A cLEAN and/or Six Sigma background is a plus
Professional proficiency in English
Moreover, understanding industrial equipment in the pharma industry or similar is essential, along with experience in automated visual inspection or image processing. Knowledge of the aseptic process is advantageous.
On a personal level, you have high integrity, are open-minded, curious, and always looking to improve processes. You are a team player and a great collaborator, using stakeholder relationships to achieve success. With a strong personal drive, you are ambitious and unafraid to challenge the status quo in a risk-adverse industry. You can drive projects from conception to effectiveness checks, communicate complex technical issues clearly, and work in a global context with manufacturing sites and headquarters.
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 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 – we’re all working to move the needle on patient care. Contact
For further information you are welcome to contact Igor Stojanovic (Project Director) on +. Deadline
25 June 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.
Then this is a unique opportunity to become part of a team of highly competent professionals and specialist impacting the way we produce diabetes products around the world. Join us and become our new Global Inspection Project Manager! About the department We are a newly established organisational unit, Aseptic Manufacturing Engineering (AME). With almost 100 colleagues, we play a key role in accelerating a major transformation to improve performance across a global network of factories in Asia, Europe as well as North and South America to meet the need of the increasing number of people living with diabetes and obesity. AME is an organizational unit in Aseptic Manufacturing (AM), which is the largest production area in . With more than 5,000 employees, AM is a truly global organization responsible for producing products for launches of all new diabetes and obesity products in supplying nearly 50% of the world’ insulin (for more information please visit Come join us in driving change for patients around the world. The position
As our new Global Inspection Project Manager, you will have the responsibility and ownership of the new fleet of Inspection lines, with focus on maintaining the standardized equipment through development and implementation in line with the global standards and asset management strategy for global Injectable Finished Products (IFP). You will report directly to the Director of the Standardized Inspection Lines Program and be part of the new department. As such, you will be able maintain a key role in establishing the set of standards and maximizing performance for the inspection line fleet for the future.
Your key responsibilities will include:
The lines will be located at existing IFP sites, with experience and knowledge of earlier generation lines. Thus, some travel is to be expected (less than 20%) along with supporting sites during office hours for the given site.
Qualifications
To succeed in this role, you have:
On a personal level, you have high integrity, are open-minded, curious, and always looking to improve processes. You are a team player and a great collaborator, using stakeholder relationships to achieve success. With a strong personal drive, you are ambitious and unafraid to challenge the status quo in a risk-adverse industry. You can drive projects from conception to effectiveness checks, communicate complex technical issues clearly, and work in a global context with manufacturing sites and headquarters.
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 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 – we’re all working to move the needle on patient care. Contact
For further information you are welcome to contact Igor Stojanovic (Project Director) on +. Deadline
25 June 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 "Projektleder", og befinder sig i kategorien "Ledelse og personale".
Arbejdsstedet er beliggende i Bagsværd.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- 06.06.2024
- Projektleder
- Bagsværd