GMP Coordinator
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Måløv
Are you passionate about having a central role in a dynamic department with tasks that involve close collaboration with many stakeholders on a daily basis? Do you have a solid understanding of Quality, Good Manufacturing Practice and Training?
If yes, you might be exactly the one we are looking for to join our team as a GMP Coordinator, apply today!
The Position
As our new GMP Coordinator, you will be the department's quality responsible who sets the direction for the department's quality level. You will be a daily sparring partner regarding quality issues, training and you will drive quality-related projects in the department, in this role you will lead and coordinate critical quality issues and compliance activities in the department and, if necessary, across.
Your main tasks will be to:
• Drive authority inspections and internal audits
• Ensure high-level GMP overview and report quality trends to management
• Work in the Quality Management System – Delivery to Quality Management Review (QMR).
• Support and challenge deviations
• Support training in the department by assigning training and building job functions/modules You will be part of a network of other GMP and training coordinators in Oral Finished Products (OFP), where you will work with many exciting tasks across the area, such as collaborating with the management team on a daily basis to ensure our quality and training targets are met. Qualifications
We are looking for a GMP coordinator who does not compromise on quality and has the drive to set the direction for the department's quality and training level.
To succeed in this role, you:
• Have a BSc or MSc in natural science, engineering or similar
• Have at least a couple years of experience from pharmaceutical industry
• Are familiar with complex quality processes and have experience from GMP-regulated areas
• Are fully proficient in both English and Danish
• Have strong communication skills Experience with LEAN is an advantage, as it is an integral part of our everyday life As a person you are able to communicate at all levels in the organization and good at solving your tasks pragmatically, also by involving your key stakeholders. It is important that you can think and act with a broad and holistic perspective and see the big picture without losing sight of important details.
About the department
Oral Finished Products (OFP), Manufacturing Development (MDev), Support and Stability employs approximately 65 highly skilled and motivated employees with the missions to bring products from late development to market production, optimize the processes and products, support the production sites, document the stability for the products and build up the documentation for authorities for new products and for marketed products. We support a broad and growing portfolio of solid dose products within Hormone Replacement Therapy (HRT), diabetes and most recently, obesity.
Working at Novo Nordisk
At Novo Nordisk, we don’t wait for change. We drive it. We are 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 to manufacturing, marketing, and sales – we’re all working to move the needle on patient care.
Contact
For further information, please contact, Mette Willer at [email protected]
Deadline
4 June 2023
Please note that we will be reviewing applications on an ongoing basis, and we encourage you to apply as soon as possible.
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.
If yes, you might be exactly the one we are looking for to join our team as a GMP Coordinator, apply today!
The Position
As our new GMP Coordinator, you will be the department's quality responsible who sets the direction for the department's quality level. You will be a daily sparring partner regarding quality issues, training and you will drive quality-related projects in the department, in this role you will lead and coordinate critical quality issues and compliance activities in the department and, if necessary, across.
Your main tasks will be to:
• Drive authority inspections and internal audits
• Ensure high-level GMP overview and report quality trends to management
• Work in the Quality Management System – Delivery to Quality Management Review (QMR).
• Support and challenge deviations
• Support training in the department by assigning training and building job functions/modules You will be part of a network of other GMP and training coordinators in Oral Finished Products (OFP), where you will work with many exciting tasks across the area, such as collaborating with the management team on a daily basis to ensure our quality and training targets are met. Qualifications
We are looking for a GMP coordinator who does not compromise on quality and has the drive to set the direction for the department's quality and training level.
To succeed in this role, you:
• Have a BSc or MSc in natural science, engineering or similar
• Have at least a couple years of experience from pharmaceutical industry
• Are familiar with complex quality processes and have experience from GMP-regulated areas
• Are fully proficient in both English and Danish
• Have strong communication skills Experience with LEAN is an advantage, as it is an integral part of our everyday life As a person you are able to communicate at all levels in the organization and good at solving your tasks pragmatically, also by involving your key stakeholders. It is important that you can think and act with a broad and holistic perspective and see the big picture without losing sight of important details.
About the department
Oral Finished Products (OFP), Manufacturing Development (MDev), Support and Stability employs approximately 65 highly skilled and motivated employees with the missions to bring products from late development to market production, optimize the processes and products, support the production sites, document the stability for the products and build up the documentation for authorities for new products and for marketed products. We support a broad and growing portfolio of solid dose products within Hormone Replacement Therapy (HRT), diabetes and most recently, obesity.
Working at Novo Nordisk
At Novo Nordisk, we don’t wait for change. We drive it. We are 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 to manufacturing, marketing, and sales – we’re all working to move the needle on patient care.
Contact
For further information, please contact, Mette Willer at [email protected]
Deadline
4 June 2023
Please note that we will be reviewing applications on an ongoing basis, and we encourage you to apply as soon as possible.
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 Måløv.
Jobbet er oprettet på vores service den 10.5.2023, 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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