QMS Process Supporter
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Bagsværd
Are you passionate about quality and want to help build the Quality Management System (QMS) of the future? Would you like to cooperate with some of our most experienced Process Managers and interact with stakeholders across the organization? Want to leverage your experience with Quality Management System from the pharma industry?
If you can say yes to the above, then there is a unique job opportunity just for you, apply now! The position
You will be part of a highly experienced team of Process Managers, whose main focus is to ensure a simple and compliant Deviation Handling process.
You will support the team with different task e.g.:
• Updating of corporate procedures, guidance, and training material
• Managing training activities
• Communication tasks
• Stakeholder management
• Providing support with digital solutions for the quality processes Moreover, together with the Process Managers, you will be handling regulatory requirements, compliance signals and be a part of small to large process related projects. This position also gives the possibility to work with other quality processes. Qualifications
The ideal candidate can bring to table expertise within QMS, quality processes and GMP knowledge, someone who can work independently as well as in a team.
To succeed in this role as, you have:
• An academic degree in pharmacy, engineering or similar
• Several years of experience working with QMS or other quality related roles in the pharmaceutical industry
• Experience working with quality processes such as Deviation Handling
• Good communication skills
• Full English proficiency On a personal level, you are robust, structured, a self-starter and a great collaborator always having a positive go-can-do attitude. The role provides excellent prospects for both personal and professional growth, with increasing responsibilities aligned with your skills and interests. About the department
Quality Processes, a part of Quality, is responsible for maintaining and continuously developing the core quality management processes and their supporting IT systems in . We are responsible for ensuring that our processes comply with the regulatory requirements, and that they operate as smoothly as possible. Our ambition is to develop and operate a robust and simple Quality Management System, that can support Novo Nordisk in maintaining world class quality in the future. You will work with 13 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.
Working at At , 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 to manufacturing, marketing, and sales – we’re all working to move the needle on patient care.
Contact For further information please contact Senior Manager Stine Akselsen at +or Deadline
1 April 2024
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.
If you can say yes to the above, then there is a unique job opportunity just for you, apply now! The position
You will be part of a highly experienced team of Process Managers, whose main focus is to ensure a simple and compliant Deviation Handling process.
You will support the team with different task e.g.:
• Updating of corporate procedures, guidance, and training material
• Managing training activities
• Communication tasks
• Stakeholder management
• Providing support with digital solutions for the quality processes Moreover, together with the Process Managers, you will be handling regulatory requirements, compliance signals and be a part of small to large process related projects. This position also gives the possibility to work with other quality processes. Qualifications
The ideal candidate can bring to table expertise within QMS, quality processes and GMP knowledge, someone who can work independently as well as in a team.
To succeed in this role as, you have:
• An academic degree in pharmacy, engineering or similar
• Several years of experience working with QMS or other quality related roles in the pharmaceutical industry
• Experience working with quality processes such as Deviation Handling
• Good communication skills
• Full English proficiency On a personal level, you are robust, structured, a self-starter and a great collaborator always having a positive go-can-do attitude. The role provides excellent prospects for both personal and professional growth, with increasing responsibilities aligned with your skills and interests. About the department
Quality Processes, a part of Quality, is responsible for maintaining and continuously developing the core quality management processes and their supporting IT systems in . We are responsible for ensuring that our processes comply with the regulatory requirements, and that they operate as smoothly as possible. Our ambition is to develop and operate a robust and simple Quality Management System, that can support Novo Nordisk in maintaining world class quality in the future. You will work with 13 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.
Working at At , 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 to manufacturing, marketing, and sales – we’re all working to move the needle on patient care.
Contact For further information please contact Senior Manager Stine Akselsen at +or Deadline
1 April 2024
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 18.3.2024, 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
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