Document Management Supporter
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Kalundborg
Novo Nordisk has announced plans to invest more than DKK42 billion to expand existing manufacturing facilities in Kalundborg, to support the current and future company portfolio within serious chronic diseases. We are hiring an experienced Document Management Supporter to join the investment project. Would you like to join a dynamic global company and work on an exciting new capacity expansion project? Are you interested in the opportunity to establish new active pharmaceutical ingredients (API) manufacturing facilities that bridges new and automated technologies with strong know-how and expertise in biotech manufacturing? The activities will be carried out at our site in Kalundborg, Novo Nordisk hub for API manufacturing. Apply today and start a life changing journey!
The Position As Document management Supporter in our API expansion projects area, you will be part of ensuring that we handle our documents in the right way. will be part of handling the project document plan and the continuous follow-up throughout the project. To be a competitive candidate, you should:
• be a part of preparing instructions and procedures to ensure the most efficient document handling in compliance with Novo Nordisk QMS
• certify that we handle new documents in correspondence with the decided structure
• ensure we have the correct structure in QualityDocs
• coordinate across the entire project to verify that plans and structures are followed by all parties Qualifications
To succeed in the position, you have:
• an administrative or technical education, e.g. lab technician
• experience in working in the Novo Nordisk GMP environment
• 2+ years of experience working with Novo Nordisk QualityDocs and other GMP systems
• proficiency within Excel
• proficiency in verbal and written English On a personal level, you possess strong communication skills, with the ability to build relationships and ensure trust and commitment from all stakeholders. With an investigative and analytical approach to problems, your accuracy of document registrations is impeccable. You enjoy teamwork and a multicultural environment that demands to also work independently. Personal drive, focus on building structure, implementing improvements and the ability to execute independently and proactively, secures that value is added where it matters within deadlines. About the department
You will become part of a small staff team called Project Quality. The mission for the team is to ensure compliance with cGMP and Novo Nordisk QMS in order to facilitate successful approval audits and inspections and a smooth transition to the operational phase within GMP and validation. The team supplies the entire API Expansion Projects area with expert knowledge on GMP, quality and Novo Nordisk validation processes. The team establishes internal processes and procedures (project Quality Management System) within validation and GEP/GMP and provides ongoing support and training. Besides this, the team is also responsible for all document management within quality for the entire area – all the way from planning a new document to the handover and archiving. About Novo Nordisk Kalundborg Since 1969, Novo Nordisk Kalundborg has been a cornerstone in our production of API. With more than 50 years of expertise in large-scale biotech manufacturing, we are today the world’s largest insulin-producing facility. Our 4,400 employees at Novo Nordisk Kalundborg produce half of the world’s insulin, and a number of biopharmaceutical products. Together, we make a difference every day for more than 35 million people living with diabetes and other chronic diseases.
Join our growing manufacturing hub in Kalundborg and gain thousands of dedicated colleagues. It is your drive and our passion, that makes a difference for their future. Are you ready for a life-changing career? Working at Novo Nordisk Novo Nordisk is a leading global healthcare company, founded in 1923 and headquartered in Denmark. Our purpose is to drive change to defeat serious chronic diseases, built upon our heritage in diabetes. We do so by pioneering scientific breakthroughs, expanding access to our medicines, and working to prevent and ultimately cure disease. Novo Nordisk employs about 61,400 people in 80 countries and markets its products in around 170 countries. Contact
For further information, please contact Senior Project Manager Mie Boa Jacobsen at +45 3075 1354. Deadline
17 December 2023. 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.
The Position As Document management Supporter in our API expansion projects area, you will be part of ensuring that we handle our documents in the right way. will be part of handling the project document plan and the continuous follow-up throughout the project. To be a competitive candidate, you should:
• be a part of preparing instructions and procedures to ensure the most efficient document handling in compliance with Novo Nordisk QMS
• certify that we handle new documents in correspondence with the decided structure
• ensure we have the correct structure in QualityDocs
• coordinate across the entire project to verify that plans and structures are followed by all parties Qualifications
To succeed in the position, you have:
• an administrative or technical education, e.g. lab technician
• experience in working in the Novo Nordisk GMP environment
• 2+ years of experience working with Novo Nordisk QualityDocs and other GMP systems
• proficiency within Excel
• proficiency in verbal and written English On a personal level, you possess strong communication skills, with the ability to build relationships and ensure trust and commitment from all stakeholders. With an investigative and analytical approach to problems, your accuracy of document registrations is impeccable. You enjoy teamwork and a multicultural environment that demands to also work independently. Personal drive, focus on building structure, implementing improvements and the ability to execute independently and proactively, secures that value is added where it matters within deadlines. About the department
You will become part of a small staff team called Project Quality. The mission for the team is to ensure compliance with cGMP and Novo Nordisk QMS in order to facilitate successful approval audits and inspections and a smooth transition to the operational phase within GMP and validation. The team supplies the entire API Expansion Projects area with expert knowledge on GMP, quality and Novo Nordisk validation processes. The team establishes internal processes and procedures (project Quality Management System) within validation and GEP/GMP and provides ongoing support and training. Besides this, the team is also responsible for all document management within quality for the entire area – all the way from planning a new document to the handover and archiving. About Novo Nordisk Kalundborg Since 1969, Novo Nordisk Kalundborg has been a cornerstone in our production of API. With more than 50 years of expertise in large-scale biotech manufacturing, we are today the world’s largest insulin-producing facility. Our 4,400 employees at Novo Nordisk Kalundborg produce half of the world’s insulin, and a number of biopharmaceutical products. Together, we make a difference every day for more than 35 million people living with diabetes and other chronic diseases.
Join our growing manufacturing hub in Kalundborg and gain thousands of dedicated colleagues. It is your drive and our passion, that makes a difference for their future. Are you ready for a life-changing career? Working at Novo Nordisk Novo Nordisk is a leading global healthcare company, founded in 1923 and headquartered in Denmark. Our purpose is to drive change to defeat serious chronic diseases, built upon our heritage in diabetes. We do so by pioneering scientific breakthroughs, expanding access to our medicines, and working to prevent and ultimately cure disease. Novo Nordisk employs about 61,400 people in 80 countries and markets its products in around 170 countries. Contact
For further information, please contact Senior Project Manager Mie Boa Jacobsen at +45 3075 1354. Deadline
17 December 2023. 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 Kalundborg.
Jobbet er oprettet på vores service den 13.11.2023, 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
- Kalundborg
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