Document Management Supporter
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Kalundborg
Document Management Supporter
Do you want to work with dedicated and experienced biotech manufacturing professionals? Do you thrive working in a GMP environment with quality in focus? Are you curious about the opportunity to establish a factory that bridges new and automated technologies with strong know-how and expertise in biotech manufacturing? Then join our team and make the most of your talent.
The activities will be carried out at our site in Kalundborg, home of Novo Nordisk API manufacturing.
Do you want to play a central role in designing the most effective and efficient document management system as well as supporting our project with support in preparing all the needed documents in due time? Are you motivated by developing new systems, concepts and procedures, continuous improvements and driving change? Then you could be the Document Management Supporter we are looking for in the API expansion Project.
To bring innovative treatments to as many patients worldwide as possible, the API expansion project investigates potential expansion of our API manufacturing capacities to support the company portfolio of future oral and injectable pharmaceuticals.
We investigate how to establish new, ground-breaking biotech facilities based on modern technology with fully automated operations and digitalised processes.
The position
About you
To succeed in the position, we expect you to have:
On a personal level, you possess strong communication skills including the ability to build relationships and ensure trust and commitment from all stakeholders. You have an investigative and analytical approach to problems and thrive at building systems and structures.
You enjoy teamwork and is a strong motivator of others. You thrive in a multicultural environment that demands independence to make critical decisions. Your personal drive, focus on building structure, implementing improvements and the ability to execute projects independently and proactively, secures that value is added where it matters and within deadlines.
About Novo Nordisk Kalundborg
Today, 3,200 employees of Novo Nordisk Kalundborg produce half of the world’s insulin and a number of biopharmaceutical products. With more than 50 years of expertise in large-scale biotech manufacturing, we are today the world’s largest insulin-producing facility. By joining Novo Nordisk Manufacturing in Kalundborg, we promise you a developing career, where you will be met with trust and responsibility by dedicated colleagues with diverse backgrounds in a successful company with a higher purpose and an inclusive environment. Together, we make a difference every day for more than 30 million people living with diabetes and other chronic diseases.
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 diabetes and other serious chronic diseases such as obesity and rare blood and endocrine disorders. We do so by pioneering scientific breakthroughs, expanding access to our medicines, and working to prevent and ultimately cure disease. Novo Nordisk employs about 53,000 people in 80 countries and markets its products in around 170 countries. For more information, visit novonordisk.com, Facebook, Twitter, LinkedIn and YouTube.
Join us from the very beginning of our future journey and make your mark on a newly established organisation that will be growing in the coming years.
Interested in a life-changing career?
Read more about the opportunities at Novo Nordisk Kalundborg at https://novonordisk.com/kalundborg-careers
Contact
For further information about the position, please contact Senior Project Manager Mie Boa Jacobsen at +45 3075 1354.
Deadline
Please apply no later than Jan 17th, 2023. We will process applications as we receive them, so please do not hesitate to apply.
You do not need to attach a cover letter to your application, but please include a few sentences about your motivation to apply in your 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.
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Do you want to work with dedicated and experienced biotech manufacturing professionals? Do you thrive working in a GMP environment with quality in focus? Are you curious about the opportunity to establish a factory that bridges new and automated technologies with strong know-how and expertise in biotech manufacturing? Then join our team and make the most of your talent.
The activities will be carried out at our site in Kalundborg, home of Novo Nordisk API manufacturing.
Do you want to play a central role in designing the most effective and efficient document management system as well as supporting our project with support in preparing all the needed documents in due time? Are you motivated by developing new systems, concepts and procedures, continuous improvements and driving change? Then you could be the Document Management Supporter we are looking for in the API expansion Project.
To bring innovative treatments to as many patients worldwide as possible, the API expansion project investigates potential expansion of our API manufacturing capacities to support the company portfolio of future oral and injectable pharmaceuticals.
We investigate how to establish new, ground-breaking biotech facilities based on modern technology with fully automated operations and digitalised processes.
The position
- As Document management supporter in our API expansion project, you will be part of ensuring that we handle our documents in the right way.
- You will be part of establishing the project document plan and then follow-up on the plan continuously throughout the project.
- You will ensure that we have the correct structure in QualityDocs and ensure that we handle new documents in correspondence with the decided structure.
- You will be part of preparing instructions and procedures to ensure the most efficient document handling in compliance with Novo Nordisk QMS.
- As part of your job, you will coordinate across the entire project in order to ensure that decided plans and structures are followed by all parties.
About you
To succeed in the position, we expect you to have:
- +2 years of experience working with Novo Nordisk QualityDocs and other GMP systems.
- Preferably a technical education, e.g., lab technician or otherwise long experience by working in the Novo Nordisk GMP environment.
- Proficiency within Excel.
- Competencies and capabilities to work independently.
- High quality mindset.
- Have English proficiency (verbal and written).
On a personal level, you possess strong communication skills including the ability to build relationships and ensure trust and commitment from all stakeholders. You have an investigative and analytical approach to problems and thrive at building systems and structures.
You enjoy teamwork and is a strong motivator of others. You thrive in a multicultural environment that demands independence to make critical decisions. Your personal drive, focus on building structure, implementing improvements and the ability to execute projects independently and proactively, secures that value is added where it matters and within deadlines.
About Novo Nordisk Kalundborg
Today, 3,200 employees of Novo Nordisk Kalundborg produce half of the world’s insulin and a number of biopharmaceutical products. With more than 50 years of expertise in large-scale biotech manufacturing, we are today the world’s largest insulin-producing facility. By joining Novo Nordisk Manufacturing in Kalundborg, we promise you a developing career, where you will be met with trust and responsibility by dedicated colleagues with diverse backgrounds in a successful company with a higher purpose and an inclusive environment. Together, we make a difference every day for more than 30 million people living with diabetes and other chronic diseases.
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 diabetes and other serious chronic diseases such as obesity and rare blood and endocrine disorders. We do so by pioneering scientific breakthroughs, expanding access to our medicines, and working to prevent and ultimately cure disease. Novo Nordisk employs about 53,000 people in 80 countries and markets its products in around 170 countries. For more information, visit novonordisk.com, Facebook, Twitter, LinkedIn and YouTube.
Join us from the very beginning of our future journey and make your mark on a newly established organisation that will be growing in the coming years.
Interested in a life-changing career?
Read more about the opportunities at Novo Nordisk Kalundborg at https://novonordisk.com/kalundborg-careers
Contact
For further information about the position, please contact Senior Project Manager Mie Boa Jacobsen at +45 3075 1354.
Deadline
Please apply no later than Jan 17th, 2023. We will process applications as we receive them, so please do not hesitate to apply.
You do not need to attach a cover letter to your application, but please include a few sentences about your motivation to apply in your 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.
Print job Send to e-mail
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 11.1.2023, 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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