Senior Manager, Compliance Portfolio Management
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Are you motivated by challenges and working in a dynamic, international, and diverse environment? Are you looking for an exciting opportunity to lead critical projects and develop global solutions?
Then this might be the right opportunity for you! Come join us as Senior Manager within IFP Manufacturing Development.
About the department
Injectable Finished Products (IFP) Compliance Portfolio Management (CPM) within Manufacturing Development (ManDev) consists of approx. 20 professional employees working with project management that enable the production sites in IFP to maintain the right level of compliance, stay on top of regulatory requirements and ensure optimised processes.
The Department is divided in two teams, Finished Product (FP) & Quality and Aseptic Production (AP) & Facility.
The position
As the Senior Manager for FP & Quality, you are key to drive corporate compliance in FP, Quality and Quality Control (QC) on behalf of IFP – a large organisation with several production sites worldwide. This will involve leading different initiations and projects across FP, Quality and QC on a global scale and ensuring compliance on our production sites.
You will chair our local governance and support and coach our employees (Project Managers/Process Managers) in their daily work. We are currently working on supporting beyond Compliance more specifically on digitalisation, standardisation, and continuous improvement in our processes.
Responsibilities will include:
You will have the opportunity to lead a team of 10 Project Managers/Process Managers who are familiar with working independently with global projects varying from small Quality Management Systems (QMS) projects to large investment projects. Therefore, a crucial part of your job is to ensure a good collaboration with stakeholders globally.
Furthermore, you will have the opportunity to travel quarterly to our sites based in Denmark, US, Brazil, and China. We require you to be based in Denmark and we are happy to discuss flexible working options related to this.
Qualifications
You are a leader who has the bigger picture in mind, sets direction, inspires, and motivates teams through driving process improvement and change. Furthermore, you are proactive, curious and have a structured approach to your work to manage and juggle work priorities.
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 – we’re all working to move the needle on patient care.
Contact
For further information, please contact Ida G. Salinas (Sr. Manager) who is heading up the AP & Facility part of CPM +45 3075 2161 or Rasmus Di Sisto Bukkehave (Director, IFP CPM & ManDev BS) on: +45 3075 7727
Deadline
1 January 2023
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.
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Then this might be the right opportunity for you! Come join us as Senior Manager within IFP Manufacturing Development.
About the department
Injectable Finished Products (IFP) Compliance Portfolio Management (CPM) within Manufacturing Development (ManDev) consists of approx. 20 professional employees working with project management that enable the production sites in IFP to maintain the right level of compliance, stay on top of regulatory requirements and ensure optimised processes.
The Department is divided in two teams, Finished Product (FP) & Quality and Aseptic Production (AP) & Facility.
The position
As the Senior Manager for FP & Quality, you are key to drive corporate compliance in FP, Quality and Quality Control (QC) on behalf of IFP – a large organisation with several production sites worldwide. This will involve leading different initiations and projects across FP, Quality and QC on a global scale and ensuring compliance on our production sites.
You will chair our local governance and support and coach our employees (Project Managers/Process Managers) in their daily work. We are currently working on supporting beyond Compliance more specifically on digitalisation, standardisation, and continuous improvement in our processes.
Responsibilities will include:
- Manage the project portfolio within the manufacturing processes.
- Drive compliance improvements, continuous improvements, digitalisation projects in the respective processes.
- Support Process Owner delegate activities to secure efficient processes across the organisation.
- Attend director group meetings and participate in different steering groups.
You will have the opportunity to lead a team of 10 Project Managers/Process Managers who are familiar with working independently with global projects varying from small Quality Management Systems (QMS) projects to large investment projects. Therefore, a crucial part of your job is to ensure a good collaboration with stakeholders globally.
Furthermore, you will have the opportunity to travel quarterly to our sites based in Denmark, US, Brazil, and China. We require you to be based in Denmark and we are happy to discuss flexible working options related to this.
Qualifications
- You hold a Master’s degree in Engineering/Chemistry/Pharmacy/Biology/Business or similar.
- Multiple years of management experience in a pharmaceutical manufacturing/ GMP environment. Experience within FP/QC/QA in manufacturing is advantageous.
- Line management experience and experience leading employees in a complex multifaceted environment.
- Excellent at collaborating with stakeholders at all levels cross functionally and globally.
- Strong communication and presentation skills with fluency in spoken and written English.
You are a leader who has the bigger picture in mind, sets direction, inspires, and motivates teams through driving process improvement and change. Furthermore, you are proactive, curious and have a structured approach to your work to manage and juggle work priorities.
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 – we’re all working to move the needle on patient care.
Contact
For further information, please contact Ida G. Salinas (Sr. Manager) who is heading up the AP & Facility part of CPM +45 3075 2161 or Rasmus Di Sisto Bukkehave (Director, IFP CPM & ManDev BS) on: +45 3075 7727
Deadline
1 January 2023
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 Bagsværd.
Jobbet er oprettet på vores service den 7.12.2022, 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
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