Quality Specialist for Inspection Office
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And would you like to coordinate paper-based inspections in collaboration with colleagues around the world?
Are you ready to take the responsibility to assess when the Danish Medicines Agency (DKMA) should be informed of major facility changes and ensure timely applications to DKMA?
Then join us in Inspection Office and get the opportunity to take our services to the next level, apply now! The position As a Quality Specialist you will be part of a dynamic environment where your job will be to support your colleagues across Novo Nordisk with quality related tasks focused on authority inspections. Your main responsibilities will be to:
• play a key role in our team maintaining and operating an IT tool for GMP requests including inspections from all our stakeholders
• have the complete overview of GMP requests and inspections to ensure all are handled and closed timely
• handle some of the GMP requests & coordinate paper-based inspections in collaboration with colleagues around the world to ensure approval of new products or new sites in different countries In this job we offer you the opportunity to grow personally and professionally by developing your GMP compliance and increasing your business insight worldwide. Qualifications To succeed in this role, you:
• hold a master's degree in chemical engineering, pharmacy, or another relevant MSc
• have several years’ experience within quality and GMP in a pharmaceutical setting
• have experience with audits/inspections
• are fluent in English Project management experience and Danish knowledge will be considered as additional plus.
As an individual, you are open-minded, structured and have an outgoing attitude. You are a strong communicator with inter-cultural understanding with the ability to handle many different priorities at the same time. You are a role model for others and dare to make tough decisions, and inspire people, but also a team player who inspires trust and respect among colleagues and partners. About the department Inspection Office is a highly specialised area where you will join a team of 14 highly skilled, ambitious and motivated specialists with the responsibility for handling all GMP inspections and notified bodies audits in Novo Nordisk.
We have a close collaboration with our stakeholders globally in Novo Nordisk spanning across manufacturing sites, affiliate offices and regulatory affairs, as well as with health authorities around the world. 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 Vice President Peter Søtofte Elten +45 3079 8453 Deadline 14 November 2023 Applications will be evaluated continuously, when received and candidates may be called for interview before the deadline.
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. 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.
Are you ready to take the responsibility to assess when the Danish Medicines Agency (DKMA) should be informed of major facility changes and ensure timely applications to DKMA?
Then join us in Inspection Office and get the opportunity to take our services to the next level, apply now! The position As a Quality Specialist you will be part of a dynamic environment where your job will be to support your colleagues across Novo Nordisk with quality related tasks focused on authority inspections. Your main responsibilities will be to:
• play a key role in our team maintaining and operating an IT tool for GMP requests including inspections from all our stakeholders
• have the complete overview of GMP requests and inspections to ensure all are handled and closed timely
• handle some of the GMP requests & coordinate paper-based inspections in collaboration with colleagues around the world to ensure approval of new products or new sites in different countries In this job we offer you the opportunity to grow personally and professionally by developing your GMP compliance and increasing your business insight worldwide. Qualifications To succeed in this role, you:
• hold a master's degree in chemical engineering, pharmacy, or another relevant MSc
• have several years’ experience within quality and GMP in a pharmaceutical setting
• have experience with audits/inspections
• are fluent in English Project management experience and Danish knowledge will be considered as additional plus.
As an individual, you are open-minded, structured and have an outgoing attitude. You are a strong communicator with inter-cultural understanding with the ability to handle many different priorities at the same time. You are a role model for others and dare to make tough decisions, and inspire people, but also a team player who inspires trust and respect among colleagues and partners. About the department Inspection Office is a highly specialised area where you will join a team of 14 highly skilled, ambitious and motivated specialists with the responsibility for handling all GMP inspections and notified bodies audits in Novo Nordisk.
We have a close collaboration with our stakeholders globally in Novo Nordisk spanning across manufacturing sites, affiliate offices and regulatory affairs, as well as with health authorities around the world. 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 Vice President Peter Søtofte Elten +45 3079 8453 Deadline 14 November 2023 Applications will be evaluated continuously, when received and candidates may be called for interview before the deadline.
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. 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 9.10.2023, 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.
- Øvrige
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