Senior Manager - Drug Product Project Management
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Måløv
Are you passionate about leading and developing highly skilled project managers who run projects for the benefit of our patients? Would you like to set the strategic direction to reach project excellence while ensuring your team is fully engaged? Do you thrive with interacting with a wide range of stakeholders across the entire organisation?
If so, this unique job opportunity is for you. Join Novo Nordisk as a Senior Manager - Drug Product Project Management.
About the department
Emerging Technologies (ET) is a newly established SVP area in . We have a growing pipeline of new products, many of which are based on emerging technology platforms coming into Product Supply via internal development projects and externally acquired assets. ET are well-known for having a pioneering spirit as well as a curious and daring approach and we play a key role in developing and producing future treatments for millions of patients around the world. The area is anchored in Product Supply, Quality & IT, which globally employ approx. 25,000 of Novo Nordisk’s 55,000 employees.
You will be joining the CVP area Drug Product Manufacturing Development & Quality Control (DP MDev & QC), which has process and product responsibility for existing and future oral drug products post-launch, as well as performing all analyses on products after method transfer. We work across the ET organization to improve productivity of our production and analytical processes. The area currently consists of 7 departments and is expanding to prepare for new drug products.
The position
In this Senior Manager role, the main responsibility will be to lead and develop highly skilled project managers who run strategic cross-functional Drug Product and Optimisation Projects. The team is anchored in our Project Office in DP MDev & QC and is expanding as more products are entering life cycle management. The team is responsible for managing and leading product- and process related product projects such as product transfers, technical upgrades, or capacity expansions within our drug product facilities and CMOs (Contract Manufacturing Organisation).
Your main responsibilities will include: Motivating, coaching, leading, and setting direction for your team
Setting up and maintaining project management structures, standards and governances to enable project management excellence
Building and maintaining strong collaboration with stakeholders across the organisation
Ownership of the drug product project portfolio across ET DP MDev & QC and ensuring strategic direction for the area
Building the team’s ability to effectively translate business priorities into operational plans
Qualifications
To succeed in this role, you have: An Academic Degree such as engineer, pharmacist, chemist, or similar scientific/technical education
Some years of experience leading strategic, complex, cross-functional projects in regulated industries combined with solid expertise as a people leader
Proven track-record in project and people leadership
Excellent stakeholder management skills
Professional proficiency in English
As an individual you thrive in engaging, motivating and inspiring your employees to perform in a dynamic and international environment. Moreover, you exhibit exceptional leadership qualities, such as being positive, open, honest, and having a holistic approach. You excel in stakeholder management, communication, and negotiation. 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. Contact
For further information, please contact Snr. Manager Mie Houlberg Danielsen at Deadline
26 May 2024. Please note that applications will be screened on an ongoing basis, therefore you are encouraged to apply as soon as possible. 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.
If so, this unique job opportunity is for you. Join Novo Nordisk as a Senior Manager - Drug Product Project Management.
About the department
Emerging Technologies (ET) is a newly established SVP area in . We have a growing pipeline of new products, many of which are based on emerging technology platforms coming into Product Supply via internal development projects and externally acquired assets. ET are well-known for having a pioneering spirit as well as a curious and daring approach and we play a key role in developing and producing future treatments for millions of patients around the world. The area is anchored in Product Supply, Quality & IT, which globally employ approx. 25,000 of Novo Nordisk’s 55,000 employees.
You will be joining the CVP area Drug Product Manufacturing Development & Quality Control (DP MDev & QC), which has process and product responsibility for existing and future oral drug products post-launch, as well as performing all analyses on products after method transfer. We work across the ET organization to improve productivity of our production and analytical processes. The area currently consists of 7 departments and is expanding to prepare for new drug products.
The position
In this Senior Manager role, the main responsibility will be to lead and develop highly skilled project managers who run strategic cross-functional Drug Product and Optimisation Projects. The team is anchored in our Project Office in DP MDev & QC and is expanding as more products are entering life cycle management. The team is responsible for managing and leading product- and process related product projects such as product transfers, technical upgrades, or capacity expansions within our drug product facilities and CMOs (Contract Manufacturing Organisation).
Your main responsibilities will include:
Qualifications
To succeed in this role, you have:
As an individual you thrive in engaging, motivating and inspiring your employees to perform in a dynamic and international environment. Moreover, you exhibit exceptional leadership qualities, such as being positive, open, honest, and having a holistic approach. You excel in stakeholder management, communication, and negotiation. 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. Contact
For further information, please contact Snr. Manager Mie Houlberg Danielsen at Deadline
26 May 2024. Please note that applications will be screened on an ongoing basis, therefore you are encouraged to apply as soon as possible. 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 Måløv.
Jobbet er oprettet på vores service den 15.5.2024, 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.
- 15.05.2024
- Øvrige
- Måløv
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