Senior GMP Supporter
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Would you like to take the next exciting step in your career by playing a key role in a dynamic and impactful business support unit, driving meaningful change in Local Manufacturing production? Does using your hands-on expertise in deviation handling and cGMP to tackle tasks, enhance processes, and elevate our quality standards inspire you? Are you passionate about improving the GMP mindset, coaching and guiding colleagues, and influencing quality decisions on a global scale?Then you might be our new Senior GMP Supporter in our office in Bagsværd! Apply today for a life-changing career!
The PositionAs a Senior GMP Supporter, you will play a central role, and your Good Manufacturing Practice (GMP) experience will have a significant impact and will be instrumental in setting direction and shaping our everyday work and support to our local production sites.In this role you will provide support, direction and guidance to Line of Business at local sites including their GMP and/or Quality partners.Even though we are office based, some travel activities can be expected based on organizational objectives and respond to urgent needs.The main tasks will be to:
• Provide Site & Project Support to our Local Manufacturing Sites, within deviation handling, quality improvements initiatives and GMP activities.
• Lead and oversee the management of more complex deviations; ensure that timely investigations, systematic problem-solving and appropriate corrective actions are implemented.
• Ensure adherence to GMP compliance requirements and best practices sharing across all operations in LM.
• Guide, train and coach sites on effective deviation handling practices to enhance compliance and operational efficiency.QualificationsTo succeed in this role, you have:
• A min. bachelor’s degree in natural science, engineering or similar field.
• Minimum +3 years of GMP experience from the pharmaceutical industry, such as tablets, assembly or packaging of finished products.
• Proven experience with LEAN and effective systematic problem-solving methodologies.
• Full professional proficiency in English, while having proficiency in Danish is nice to have.As a person, you have strong stakeholder management skills and can set clear direction within GMP, Quality mindset and behaviour. Being a strong team player, who can easily build relationships and partnerships is crucial in this role.We will welcome a colleague who is proud of having great communication skills, the ability to understand and act within foreign cultures, while also fostering teamwork, knowledge sharing and collaboration across our global organization.About the DepartmentLocal Manufacturing - Projects and site Support, is part of LM Business Support, Denmark and our primary role is the establishment and operation of local manufacturing sites in countries where local presence is required to obtain market access.We are overseeing our local production sites in Algeria, Russia, Iran, and Japan and provide quality and project sup-port to our local factories on a daily basic. The Project and site Support team consists of specialists, professionals and project managers, providing support and guidance within Quality, Audit and Inspections and Production Processes (FPM).We have high ambitions and aim, as a team, to raise the quality and performance level at our Local Sites. We are 23 employees in the entire department in Denmark and we are currently located in Bagsværd.Working at 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 , 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 For further information, please contact Senior Manager Projects and Site support Karin Løbel-Moberg at +or via email at 27 April 2025.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 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.
The PositionAs a Senior GMP Supporter, you will play a central role, and your Good Manufacturing Practice (GMP) experience will have a significant impact and will be instrumental in setting direction and shaping our everyday work and support to our local production sites.In this role you will provide support, direction and guidance to Line of Business at local sites including their GMP and/or Quality partners.Even though we are office based, some travel activities can be expected based on organizational objectives and respond to urgent needs.The main tasks will be to:
• Provide Site & Project Support to our Local Manufacturing Sites, within deviation handling, quality improvements initiatives and GMP activities.
• Lead and oversee the management of more complex deviations; ensure that timely investigations, systematic problem-solving and appropriate corrective actions are implemented.
• Ensure adherence to GMP compliance requirements and best practices sharing across all operations in LM.
• Guide, train and coach sites on effective deviation handling practices to enhance compliance and operational efficiency.QualificationsTo succeed in this role, you have:
• A min. bachelor’s degree in natural science, engineering or similar field.
• Minimum +3 years of GMP experience from the pharmaceutical industry, such as tablets, assembly or packaging of finished products.
• Proven experience with LEAN and effective systematic problem-solving methodologies.
• Full professional proficiency in English, while having proficiency in Danish is nice to have.As a person, you have strong stakeholder management skills and can set clear direction within GMP, Quality mindset and behaviour. Being a strong team player, who can easily build relationships and partnerships is crucial in this role.We will welcome a colleague who is proud of having great communication skills, the ability to understand and act within foreign cultures, while also fostering teamwork, knowledge sharing and collaboration across our global organization.About the DepartmentLocal Manufacturing - Projects and site Support, is part of LM Business Support, Denmark and our primary role is the establishment and operation of local manufacturing sites in countries where local presence is required to obtain market access.We are overseeing our local production sites in Algeria, Russia, Iran, and Japan and provide quality and project sup-port to our local factories on a daily basic. The Project and site Support team consists of specialists, professionals and project managers, providing support and guidance within Quality, Audit and Inspections and Production Processes (FPM).We have high ambitions and aim, as a team, to raise the quality and performance level at our Local Sites. We are 23 employees in the entire department in Denmark and we are currently located in Bagsværd.Working at 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 , 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 For further information, please contact Senior Manager Projects and Site support Karin Løbel-Moberg at +or via email at 27 April 2025.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 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 31.3.2025, 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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