QA Professional in IFP QA Imported Products
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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. Read on and apply for a life-changing career! The position
Your key responsibility would be, together with your colleagues, to ensure that our documentation is following internal and external requirements. You will do this by reviewing documents from the production sites along with documentation for the supporting processes such as temperature monitoring etc.
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 QA organisation but also international colleagues. You will have numerous daily encounters with both national and international colleagues, and you can expect a high level of complexity and independent decision making in your daily tasks. If you are looking for a job which can foster the development of your professional and personal competences, this may be your opportunity. Qualifications
We seek a colleague who fits together with the team both professional and personal. As a person you are open, honest, forthcoming, and inclusive regarding your colleagues in both QA and the production. You enjoy working in a dynamic environment where you can take responsibility and take action.
In addition, you:
• Hold a Master´s degree in Pharmacy or corresponding education (for example MSc. Chem Eng or MSc. Biology
• Ideally, have knowledge about GMP
• Share our passion for quality, problem solving and LEAN and are keen to acquire professional competencies and learn the tricks of the trade
• Are fluent in Danish and English
It will be an advantage if you have experience with QA, batch release or aseptic production.
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.
About the department IFP QA Site BA is a department, consisting of approx. 60 dedicated and engaged employees situated in Bagsværd. The department is divided into 4 teams and the open position is in the QA team responsible for release of products imported into EU. 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.
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. Working at Novo Nordisk
Founded in Denmark in 1923, Novo Nordisk has become one of the world's leading healthcare companies. At Novo Nordisk, we are committed to driving change to defeat diabetes and other serious chronic diseases. To fulfill this purpose, we pioneer scientific breakthroughs, expand access to our medicines, and work to prevent and ultimately cure disease. That said, we are anything but linear. With us, your skills, commitment, and ambition help us change patients' lives worldwide. In exchange, we offer you a rewarding and purpose-driven culture with talented and diverse co-workers. Therefore, your professional and personal development is essential for us. In Novo Nordisk, the sky is the limit for career opportunities. Contact
For further information contact Christina Grebin Rosenkilde at +45 3079 9624 Deadline
6th May 2024
To ensure an efficient and fair process, please refrain from including a photo of yourself 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.
If so, there is an exciting job opportunity in Injectable Finished Products (IFP) QA. Read on and apply for a life-changing career! The position
Your key responsibility would be, together with your colleagues, to ensure that our documentation is following internal and external requirements. You will do this by reviewing documents from the production sites along with documentation for the supporting processes such as temperature monitoring etc.
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 QA organisation but also international colleagues. You will have numerous daily encounters with both national and international colleagues, and you can expect a high level of complexity and independent decision making in your daily tasks. If you are looking for a job which can foster the development of your professional and personal competences, this may be your opportunity. Qualifications
We seek a colleague who fits together with the team both professional and personal. As a person you are open, honest, forthcoming, and inclusive regarding your colleagues in both QA and the production. You enjoy working in a dynamic environment where you can take responsibility and take action.
In addition, you:
• Hold a Master´s degree in Pharmacy or corresponding education (for example MSc. Chem Eng or MSc. Biology
• Ideally, have knowledge about GMP
• Share our passion for quality, problem solving and LEAN and are keen to acquire professional competencies and learn the tricks of the trade
• Are fluent in Danish and English
It will be an advantage if you have experience with QA, batch release or aseptic production.
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.
About the department IFP QA Site BA is a department, consisting of approx. 60 dedicated and engaged employees situated in Bagsværd. The department is divided into 4 teams and the open position is in the QA team responsible for release of products imported into EU. 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.
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. Working at Novo Nordisk
Founded in Denmark in 1923, Novo Nordisk has become one of the world's leading healthcare companies. At Novo Nordisk, we are committed to driving change to defeat diabetes and other serious chronic diseases. To fulfill this purpose, we pioneer scientific breakthroughs, expand access to our medicines, and work to prevent and ultimately cure disease. That said, we are anything but linear. With us, your skills, commitment, and ambition help us change patients' lives worldwide. In exchange, we offer you a rewarding and purpose-driven culture with talented and diverse co-workers. Therefore, your professional and personal development is essential for us. In Novo Nordisk, the sky is the limit for career opportunities. Contact
For further information contact Christina Grebin Rosenkilde at +45 3079 9624 Deadline
6th May 2024
To ensure an efficient and fair process, please refrain from including a photo of yourself 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 Bagsværd.
Jobbet er oprettet på vores service den 4.3.2024, 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
- Bagsværd
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