Senior QMS Professional
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Måløv
Are you ready to make a difference for people living with diabetes and be part of the tablet production in Emerging Technologies (ET). ET is now looking for a QMS Professional, who is passionate about quality and want to help build, improve, and maintain the ET Quality Management System. Would you like to cooperate and interact with stakeholders across ET and Novo Nordisk? If so, there is a unique job opportunity and great colleagues waiting for you! The position In this role, as a Quality Professional, you will support the ET organization and QA in achieving and maintaining the “license to operate” by setting direction and level within GMP and Compliance. This means that you will: • Drive and implement GMP projects across ET, where the majority your role will be to improve processes, here you will have a chance to challenge and improve your project management skills across various projects and departments across ET
• Guide and navigate in maintaining, updating, and improving the current ET Quality Management System (QMS) processes and find optimal solutions, while navigating in internal and external requirements
• Promote simplicity and cross-site harmonization, which be across ET, PS (Product Supply), and where else relevant in Novo Nordisk
• You are also expected to build and maintain a good relationship with your wide range of stakeholders across the ET organization and the wider Novo Nordisk to set the strategic direction of QMS and other initiatives relevant for the team, i.e. in production departments, Quality Assurance, Quality Control and Technical Support in Denmark and the US
Qualifications To succeed in this role, you will need:
• You hold an academic degree, preferably as Engineering, Pharmacy, Chemistry, Biology, Biopharmaceutics and similar
• You have relevant work experience from the medical device or pharmaceutical industry within QMS, Quality Assurance, production or similar
• You have experience driving or being part of projects and process improvement
• You have a high level of fluency in written and spoken English, and Danish would be an advantage
• You also have a strong quality, proactive, pragmatic mindset, and you are used to work in fast environments
• You have strong stakeholder management skills On a personal level, you are ambitious, curious, proactive and have a strong interest in developing yourself and people in your network. You demonstrate a service-minded attitude, independence, a focus on simplicity and a sense of responsibility for your tasks. Finally, you exhibit excellent communication skills, enabling effective collaboration with individuals from diverse nationalities and cultures.
About the department ET is anchored in Product Supply, which globally address 26,000 of Novo Nordisk’s 55,000 employees. In ET, we are more than 1600 dedicated employees based primarily in Måløv (DK), but also in Durham (US) - and our sites are still growing. For the future we have many ambitions, and we are working hard to get our new tablet product on the market. Together we will succeed and still strive being at the forefront of the development of technology, systems, and processes etc.
You will join the QMS Team, part of the “Strategy & Operational Excellence” department based in Måløv, and we will be reallocating in autumn 2024 to Taarstrup. In the QMS Team, it is our main responsibility to deliver support of highest possible quality to the organization and to maintain/develop ET’s Quality Management System by ensuring efficiency and applicability in our QMS processes. We work together across the team and with colleagues across ET to continuously develop and improve our standards in order to provide aligned and effective tools that support a stable and compliant production.
In ET, we make a huge effort for you as a new employee to be off to a good start. During the first few days you will spend some time with other new employees, where you will go through an exciting introduction plan together. We know how important it is, and we are looking forward to meeting you. 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 hiring manager Yasemin Göncü, Associate Manager at [email protected]
Deadline
12 May 2024. Please note that applications will be reviewed continuously, and interviews will be planned as soon as suitable candidates have been identified. 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.
• Guide and navigate in maintaining, updating, and improving the current ET Quality Management System (QMS) processes and find optimal solutions, while navigating in internal and external requirements
• Promote simplicity and cross-site harmonization, which be across ET, PS (Product Supply), and where else relevant in Novo Nordisk
• You are also expected to build and maintain a good relationship with your wide range of stakeholders across the ET organization and the wider Novo Nordisk to set the strategic direction of QMS and other initiatives relevant for the team, i.e. in production departments, Quality Assurance, Quality Control and Technical Support in Denmark and the US
Qualifications To succeed in this role, you will need:
• You hold an academic degree, preferably as Engineering, Pharmacy, Chemistry, Biology, Biopharmaceutics and similar
• You have relevant work experience from the medical device or pharmaceutical industry within QMS, Quality Assurance, production or similar
• You have experience driving or being part of projects and process improvement
• You have a high level of fluency in written and spoken English, and Danish would be an advantage
• You also have a strong quality, proactive, pragmatic mindset, and you are used to work in fast environments
• You have strong stakeholder management skills On a personal level, you are ambitious, curious, proactive and have a strong interest in developing yourself and people in your network. You demonstrate a service-minded attitude, independence, a focus on simplicity and a sense of responsibility for your tasks. Finally, you exhibit excellent communication skills, enabling effective collaboration with individuals from diverse nationalities and cultures.
About the department ET is anchored in Product Supply, which globally address 26,000 of Novo Nordisk’s 55,000 employees. In ET, we are more than 1600 dedicated employees based primarily in Måløv (DK), but also in Durham (US) - and our sites are still growing. For the future we have many ambitions, and we are working hard to get our new tablet product on the market. Together we will succeed and still strive being at the forefront of the development of technology, systems, and processes etc.
You will join the QMS Team, part of the “Strategy & Operational Excellence” department based in Måløv, and we will be reallocating in autumn 2024 to Taarstrup. In the QMS Team, it is our main responsibility to deliver support of highest possible quality to the organization and to maintain/develop ET’s Quality Management System by ensuring efficiency and applicability in our QMS processes. We work together across the team and with colleagues across ET to continuously develop and improve our standards in order to provide aligned and effective tools that support a stable and compliant production.
In ET, we make a huge effort for you as a new employee to be off to a good start. During the first few days you will spend some time with other new employees, where you will go through an exciting introduction plan together. We know how important it is, and we are looking forward to meeting you. 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 hiring manager Yasemin Göncü, Associate Manager at [email protected]
Deadline
12 May 2024. Please note that applications will be reviewed continuously, and interviews will be planned as soon as suitable candidates have been identified. 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.
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 23.4.2024, 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
- Måløv
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