Quality Management Systems Specialist
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Are you passionate about quality and want to help driving the quality processes in Novo Nordisk? Would you like to cooperate with some of our most experienced Process Managers and interact with stakeholders across the organization? If so, there is a unique job opportunity waiting for you, read more and apply now!
About the department
Quality Processes, a part of Novo Nordisk Quality, is responsible for maintaining and continuously developing the core quality management processes and their supporting IT systems in Novo Nordisk. We are responsible for ensuring that our processes are in compliance with the regulatory requirements, and that they operate as smoothly as possible. Our ambition is to develop a robust and simple quality management system, that can support Novo Nordisk in maintaining world class quality in the future. You will work with 11 committed team members and will report to the Senior Manager in QMS Operations. The position is anchored in Bagsværd, but in collaboration with stakeholders from all around the globe.
The position
You will work as a Process Manager for Quality Monitoring Trends and work closely together with other Process Managers, and have the back-up role for other processes e.g. the deviation process. In this role, you will:
• head up the Quality Monotoring Trend corporate process group
• head up our Corrective Actions and Preventive Actions (CAPA) System Governance Group, driving alignment between the CAPA processes to benefit our end-users
• secure compliance with regulatory requirements
• develop the process & training strategy
• together with the process owner, drive and develop the corporate process group
• be responsible for drafting up procedure and relevant instructions We are on a journey implementing a new IT System for our quality processes. This position provides a unique opportunity to impact our quality processes and the business and together with the corporate process group drive implementation of a new IT system impacting all Novo Nordisk. Qualifications
We are looking for someone with knowledge of QMS processes, experience with investigations of quality problems, and who knows how to set up trending, or monitoring of quality processes with ease. Where others see barriers and problems you find solutions that are smart, - and you are able to easily explain these to your peers. To succeed in this role, you:
• have a master’s degree within pharmacy, engineering or similar
• have several years of experience working with processes from production or quality
• have profound knowledge of GMP rules and extensive hands-on experience with quality management processes
• have excellent stakeholder management and communication skills
• are fluent in English Experience with facilitating workshops from e.g. project management will be seen as an advantage. Your personal qualities define you as robust, structured, a self-starter and a great collaborator always having a positive attitude. You have an eye for the details, yet at the same time manage to set things in perspective and see the big picture. You are known for your high-quality work, your positive attitude and your ability to quickly obtain an overview of a given subject. Working at Novo Nordisk
We are a proud life-science company, and life is our reason to exist. We’re inspired by life in all its forms and shapes, ups and downs, opportunities and challenges. For employees at Novo Nordisk, life means many things – from the building blocks of life that form the basis of ground-breaking scientific research, to our rich personal lives that motivate and energise us to perform our best at work. Ultimately, life is why we’re all here - to ensure that people can lead a life independent of chronic disease. Contact
If this opportunity sounds like a great fit for you, please contact Director Birthe Ross for further information at +45 3075 6503. Deadline
1 August 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.
About the department
Quality Processes, a part of Novo Nordisk Quality, is responsible for maintaining and continuously developing the core quality management processes and their supporting IT systems in Novo Nordisk. We are responsible for ensuring that our processes are in compliance with the regulatory requirements, and that they operate as smoothly as possible. Our ambition is to develop a robust and simple quality management system, that can support Novo Nordisk in maintaining world class quality in the future. You will work with 11 committed team members and will report to the Senior Manager in QMS Operations. The position is anchored in Bagsværd, but in collaboration with stakeholders from all around the globe.
The position
You will work as a Process Manager for Quality Monitoring Trends and work closely together with other Process Managers, and have the back-up role for other processes e.g. the deviation process. In this role, you will:
• head up the Quality Monotoring Trend corporate process group
• head up our Corrective Actions and Preventive Actions (CAPA) System Governance Group, driving alignment between the CAPA processes to benefit our end-users
• secure compliance with regulatory requirements
• develop the process & training strategy
• together with the process owner, drive and develop the corporate process group
• be responsible for drafting up procedure and relevant instructions We are on a journey implementing a new IT System for our quality processes. This position provides a unique opportunity to impact our quality processes and the business and together with the corporate process group drive implementation of a new IT system impacting all Novo Nordisk. Qualifications
We are looking for someone with knowledge of QMS processes, experience with investigations of quality problems, and who knows how to set up trending, or monitoring of quality processes with ease. Where others see barriers and problems you find solutions that are smart, - and you are able to easily explain these to your peers. To succeed in this role, you:
• have a master’s degree within pharmacy, engineering or similar
• have several years of experience working with processes from production or quality
• have profound knowledge of GMP rules and extensive hands-on experience with quality management processes
• have excellent stakeholder management and communication skills
• are fluent in English Experience with facilitating workshops from e.g. project management will be seen as an advantage. Your personal qualities define you as robust, structured, a self-starter and a great collaborator always having a positive attitude. You have an eye for the details, yet at the same time manage to set things in perspective and see the big picture. You are known for your high-quality work, your positive attitude and your ability to quickly obtain an overview of a given subject. Working at Novo Nordisk
We are a proud life-science company, and life is our reason to exist. We’re inspired by life in all its forms and shapes, ups and downs, opportunities and challenges. For employees at Novo Nordisk, life means many things – from the building blocks of life that form the basis of ground-breaking scientific research, to our rich personal lives that motivate and energise us to perform our best at work. Ultimately, life is why we’re all here - to ensure that people can lead a life independent of chronic disease. Contact
If this opportunity sounds like a great fit for you, please contact Director Birthe Ross for further information at +45 3075 6503. Deadline
1 August 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.
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 23.6.2023, 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.
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