Manager for Analytical Validation Team
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Gentofte
Would you be excited to lead a group of very skilled employees in one of our validation teams? Are you motivated by playing a significant role in getting products ready for the market? And do you have excellent communication and stakeholder management skills?
Then you might be the new Manager for our Analytical Validation Team 1. Apply now and join us!
The position
As our Analytical Validation Team has grown too big for one manager, we will split the team into 2 teams, and we need an additional manager for one of the teams. You will be responsible for ensuring that employees thrive and grow and make best use of their competences to ensure our analytical methods and processes meet the highest quality standards.
Your main responsibilities will include: Direct leadership and management of approximately 10 employees Allocating and prioritizing resources to ensure that project milestones are met Short- and long-term planning of tasks Stakeholder management and strategic work Supporting your team members in developing and implementing analytical validation strategies and plans to ensure that our analytical methods and processes meet customer requirements and regulatory standards
Furthermore, you will collaborate with stakeholders and cross-functional teams to ensure that analytical validation activities are integrated into the product development process. Many of the tasks will be planned and performed in close collaboration with the manager of Analytical Validation Team 2 and the department's management team. Qualifications
To succeed in this role, we expect you to have: A MSc degree within Analytical Chemistry, Biochemistry, Pharmacy, or similar relevant discipline combined with solid GMP knowledge Experience from 2-5 years as manager in the pharmaceutical or biotech industry. Strong leadership and management skills Excellent communication and interpersonal skills Full proficiency in oral and written English and the ability to communicate and understand Danish
On a personal level you are empathic, motivating and can easily connect with people at all levels of the organization. Whilst you enjoy working independently, you also see yourself as a team player with a great ability to build strong working relations and take charge of a group.
About the Department
Our department is named Analytical Manufacturing Development, and we are situated in Gentofte close to Copenhagen. We are around 75 colleagues who are responsible for supporting QC with new analytical technology and automation and we validate analytical methods during transfer from CMC to QC. We manage the analytical part of projects when new products are handed over from CMC. Throughout life cycle management, we ensure excellent internal and external analytical documentation of a portfolio of products, and we ensure presence and documentation of reference materials for the products. A complex and fantastic department to work in. Working at Novo Nordisk
Analytical Manufacturing Development is part of Novo Nordisk Product Supply, which is a global production network at the forefront of technology and quality production of pharmaceutical products. We are not only supplying all Novo Nordisk products to people living with serious chronic diseases, but we also use our competences in biotech to support the growing efforts into completely new production platforms and therapy areas for Novo Nordisk.
We are more than 3000 dedicated colleagues working at six production sites in Denmark and the United States. Here we cover the entire production value chain where raw materials are cultivated, purified, formulated, filled, assembled in devices, packed, and distributed across the globe. As more and more people need our products, we support Novo Nordisk's initiatives in new therapy areas. Every day, we work to streamline and expand our capacity through process innovation, automation, and the introduction of new technology. Contact
For further information, please do not hesitate to contact Ann Mürer at +45 3075 7796. Deadline 19 June 2024. 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.
Then you might be the new Manager for our Analytical Validation Team 1. Apply now and join us!
The position
As our Analytical Validation Team has grown too big for one manager, we will split the team into 2 teams, and we need an additional manager for one of the teams. You will be responsible for ensuring that employees thrive and grow and make best use of their competences to ensure our analytical methods and processes meet the highest quality standards.
Your main responsibilities will include:
Furthermore, you will collaborate with stakeholders and cross-functional teams to ensure that analytical validation activities are integrated into the product development process. Many of the tasks will be planned and performed in close collaboration with the manager of Analytical Validation Team 2 and the department's management team. Qualifications
To succeed in this role, we expect you to have:
On a personal level you are empathic, motivating and can easily connect with people at all levels of the organization. Whilst you enjoy working independently, you also see yourself as a team player with a great ability to build strong working relations and take charge of a group.
About the Department
Our department is named Analytical Manufacturing Development, and we are situated in Gentofte close to Copenhagen. We are around 75 colleagues who are responsible for supporting QC with new analytical technology and automation and we validate analytical methods during transfer from CMC to QC. We manage the analytical part of projects when new products are handed over from CMC. Throughout life cycle management, we ensure excellent internal and external analytical documentation of a portfolio of products, and we ensure presence and documentation of reference materials for the products. A complex and fantastic department to work in. Working at Novo Nordisk
Analytical Manufacturing Development is part of Novo Nordisk Product Supply, which is a global production network at the forefront of technology and quality production of pharmaceutical products. We are not only supplying all Novo Nordisk products to people living with serious chronic diseases, but we also use our competences in biotech to support the growing efforts into completely new production platforms and therapy areas for Novo Nordisk.
We are more than 3000 dedicated colleagues working at six production sites in Denmark and the United States. Here we cover the entire production value chain where raw materials are cultivated, purified, formulated, filled, assembled in devices, packed, and distributed across the globe. As more and more people need our products, we support Novo Nordisk's initiatives in new therapy areas. Every day, we work to streamline and expand our capacity through process innovation, automation, and the introduction of new technology. Contact
For further information, please do not hesitate to contact Ann Mürer at +45 3075 7796. Deadline 19 June 2024. 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.
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Gentofte.
Jobbet er oprettet på vores service den 23.2.2024, 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.
- Øvrige
- Gentofte
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Statistik over udbudte øvrige i Gentofte over tid
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