Process Manager for Batch Records and Review
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Would you like to set direction for requirements for batch records and review on a corporate level in collaboration with colleagues around the world? Are you ready to take the responsibility and use your project management skills?
Then join us in Inspection Office and get the opportunity to take our processes to the next level, apply now for a life-changing career! The position
As a process manager 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 Batch records, review and release. Your main responsibilities will be to:
• Establish process group to drive improvements of our process for batch records
• Ensure current and future regulatory requirements are covered by the process
• Work with stakeholders across the organisation to ensure the process supports the growth of the company 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 M.Sc
• Have several years’ experience within quality and GMP in a pharmaceutical setting
• Have experience with pharmaceutical manufacturing, batch release, and related documentation
• Are fluent in English Having project management experience and Danish language skills 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 and global stakeholders 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 18 highly skilled, ambitious, and motivated specialists with the responsibility for handling all GMP inspections and notified bodies audits in Novo Nordisk as well as responsibility for the corporate Batch records, review and release processes. 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 at +45 3079 8453 Deadline
20th April 2024. Applications will be evaluated continuously.
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.
Then join us in Inspection Office and get the opportunity to take our processes to the next level, apply now for a life-changing career! The position
As a process manager 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 Batch records, review and release. Your main responsibilities will be to:
• Establish process group to drive improvements of our process for batch records
• Ensure current and future regulatory requirements are covered by the process
• Work with stakeholders across the organisation to ensure the process supports the growth of the company 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 M.Sc
• Have several years’ experience within quality and GMP in a pharmaceutical setting
• Have experience with pharmaceutical manufacturing, batch release, and related documentation
• Are fluent in English Having project management experience and Danish language skills 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 and global stakeholders 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 18 highly skilled, ambitious, and motivated specialists with the responsibility for handling all GMP inspections and notified bodies audits in Novo Nordisk as well as responsibility for the corporate Batch records, review and release processes. 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 at +45 3079 8453 Deadline
20th April 2024. Applications will be evaluated continuously.
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 17.2.2024, 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
- Bagsværd
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