Quality Assurance Professional
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Do you want to use your strong quality mind-set and great interpersonal skills to make a difference within QA? Are you eager to play an important role in ensuring the quality and safety of our products? If so, there is an exciting job opportunity in Injectable Finished Products (IFP) QA which fits perfectly for you.
About the Department
IFP QA Site BA is a department, consisting of approx. 60 dedicated and engaged employees situated in Bagsværd. Our department ensures a high level of quality in close cooperation with our stakeholders. Our responsibility is to assure product quality and regulatory compliance by defining quality requirements, perform quality oversight and by approving quality documents such as procedures, change request and batch- & validation documents. We participate in systematic problem solving and approve deviations. The department is furthermore responsible for assuring the quality of implementation of new equipment and new products in the production facility.
The position Your key responsibility is, together with your colleagues, to ensure that our documentation is in compliance with internal and external requirements. You will do this by reviewing core documents from the aseptic production along with documentation for the supporting processes such as environmental monitoring and utility. You will also be responsible for approving deviations and participate in QA oversight as our department is present in the production every day. As a QA professional, you will play a central role where you need to make decisions and set directions for quality. This demands good collaboration skills and a solution-oriented approach when collaborating with colleagues both in the production and QA. We have a positive working environment with a desire and a will to solve challenges through open and honest dialogue. We work together as a team because we ensure collaboration across competences and take care of each other. We always work on improving our way of working and we appreciate new ideas and continues improvements.
Qualifications We seek a colleague who fits together with the team both professionally and personally. As a person you are open, honest, forthcoming and inclusive regarding your colleagues. You enjoy working in a dynamic environment where you take responsibility and take action. You must have a Master´s degree in Pharmacy or corresponding education (for example MSc. Chem Eng or MSc. Biology) and ideally, you have knowledge about GMP. Most importantly, you share our passion for quality, problem solving and LEAN and are keen to acquire professional competencies and learn the tricks of the trade. You dare to challenge us in our way of working and has a desire to take initiative as well as being responsible for your own learning. It will be an advantage if you have experience with QA, batch release or aseptic production. The position requires you to speak fluent Danish and have proficiency in English as our documentation from production is mainly written in Danish. Working at Novo Nordisk At Novo Nordisk it is your skills, your commitment, and your ambitions that help us improve many people's lives. In return, we offer you the opportunity to work with exceptionally talented colleagues, and we offer you a wide range of opportunities for professional and personal development.
If you wish to learn more about working at Novo Nordisk, we invite you to find information here link: http://www.novonordisk.com/careers/working-at-novo-nordisk.html
Contact
For further information contact Louise Vilstrup Thøgersen +45 3079 5546 Deadline
26th September 2023 Interviews will be held on an ongoing basis To ensure an efficient and fair process, please refrain from including a photo of yourself in your CV.
Millions rely on us
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronic diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development. 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.
About the Department
IFP QA Site BA is a department, consisting of approx. 60 dedicated and engaged employees situated in Bagsværd. Our department ensures a high level of quality in close cooperation with our stakeholders. Our responsibility is to assure product quality and regulatory compliance by defining quality requirements, perform quality oversight and by approving quality documents such as procedures, change request and batch- & validation documents. We participate in systematic problem solving and approve deviations. The department is furthermore responsible for assuring the quality of implementation of new equipment and new products in the production facility.
The position Your key responsibility is, together with your colleagues, to ensure that our documentation is in compliance with internal and external requirements. You will do this by reviewing core documents from the aseptic production along with documentation for the supporting processes such as environmental monitoring and utility. You will also be responsible for approving deviations and participate in QA oversight as our department is present in the production every day. As a QA professional, you will play a central role where you need to make decisions and set directions for quality. This demands good collaboration skills and a solution-oriented approach when collaborating with colleagues both in the production and QA. We have a positive working environment with a desire and a will to solve challenges through open and honest dialogue. We work together as a team because we ensure collaboration across competences and take care of each other. We always work on improving our way of working and we appreciate new ideas and continues improvements.
Qualifications We seek a colleague who fits together with the team both professionally and personally. As a person you are open, honest, forthcoming and inclusive regarding your colleagues. You enjoy working in a dynamic environment where you take responsibility and take action. You must have a Master´s degree in Pharmacy or corresponding education (for example MSc. Chem Eng or MSc. Biology) and ideally, you have knowledge about GMP. Most importantly, you share our passion for quality, problem solving and LEAN and are keen to acquire professional competencies and learn the tricks of the trade. You dare to challenge us in our way of working and has a desire to take initiative as well as being responsible for your own learning. It will be an advantage if you have experience with QA, batch release or aseptic production. The position requires you to speak fluent Danish and have proficiency in English as our documentation from production is mainly written in Danish. Working at Novo Nordisk At Novo Nordisk it is your skills, your commitment, and your ambitions that help us improve many people's lives. In return, we offer you the opportunity to work with exceptionally talented colleagues, and we offer you a wide range of opportunities for professional and personal development.
If you wish to learn more about working at Novo Nordisk, we invite you to find information here link: http://www.novonordisk.com/careers/working-at-novo-nordisk.html
Contact
For further information contact Louise Vilstrup Thøgersen +45 3079 5546 Deadline
26th September 2023 Interviews will be held on an ongoing basis To ensure an efficient and fair process, please refrain from including a photo of yourself in your CV.
Millions rely on us
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronic diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development. 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 Bagsværd.
Jobbet er oprettet på vores service den 14.9.2023, 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
- Bagsværd
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