QA Specialist for IFP QA - FP Expansion
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Kalundborg
Would you like to be part of an exciting innovation journey to implement new FP production lines across IFP worldwide at Novo Nordisk? Do you have a strong quality mind-set and great interpersonal skills to make a difference within Quality Assurance? Then there is a challenging job opportunity in Injectable Finished Products (IFP) QA Kalundborg.
We are searching for QA Specialists, with a high level of dedication and an innovative mindset who thrives in a constantly changing and challenging environment. You will be a part of helping IFP to succeed with implementation of new assembly and packing lines across the world.
Would you like to be part of a newly established team and have a huge impact on how the team will operate in the future? Do you find it exiting to be part of a global Q setup, that is going to support IFP in implementing of new assembly and packaging lines across the world?
Then you need to apply for this fantastic opportunity.
New FP expansion team will be responsible for the global approach for the FP expansion projects across IFP and support a standardized design and requirement setup for all new FP lines.
The position
You will be part of a newly establish team, with the responsibilities of setting direction, approving documentation and keep oversight in relation to validation of all new FP lines across IFP. The team have the responsibility of QA review and oversight of several types of documents related to validation and qualification, to ensure product quality and compliance with the current GMP rules and guidelines.
You will have a role as Q-lead for one or more projects, where you will work closely together with several stakeholders across the world within DMD (Device Manufacturing Development), IFP and IFPQA, to ensure implementation of all new FP lines, with highest quality to patient in mind.
On top of that QA is a major player at internal audits and external authority inspections where you are expected to participate and present data when needed.
We can offer you a lot of freedom in planning your daily tasks, as well as occasionally working from home, when it fits into the operation and your peers in the team.
Qualifications
You hold a Master’s degree in engineering, pharmacy or similar and have solid experience within the pharmaceutical industry. You are able to set a clear direction, with reliable argumentation. Huge experience with quality assurance and/or production will be an advantage together with the right quality mindset.
You are ambitious and ready to be part of improving our high standards. 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. You are a dedicated team player who inspires trust and respect amongst colleagues and stakeholders. We are cooperating broadly with many stakeholders and therefore excellent collaboration and communication skills are needed.
We operate in an international company and the position therefore requires proficiency in English.
About the department
Our Quality assurance department consist of 25 dedicated employees, and we are still growing and soon we will be 30 employees. Our department is responsible for assuring quality and compliance of FP operations and support the business by improving and simplifying processes. Our department releases life saving Novo Nordisk products to our patients every day and we have a strong cooperation with our stakeholders to make this happen.
We are looking into a future where new production lines need to be implemented, to help Novo Nordisk succeed with the rising demand of our products from our patients. In order to succeed, this requires a Quality department with a high level of commitment to ensure highest quality to our patient, even when we are challenged during project execution and daily operation.
Working at Novo Nordisk
At Novo Nordisk, your skills, dedication, and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.
Contact
For further information, please contact Mette Lise Christensen +45 30752664.
Deadline
20th of January 2023.
Applications will be screened on an ongoing basis, so you are encouraged to apply as soon as possible.
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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We are searching for QA Specialists, with a high level of dedication and an innovative mindset who thrives in a constantly changing and challenging environment. You will be a part of helping IFP to succeed with implementation of new assembly and packing lines across the world.
Would you like to be part of a newly established team and have a huge impact on how the team will operate in the future? Do you find it exiting to be part of a global Q setup, that is going to support IFP in implementing of new assembly and packaging lines across the world?
Then you need to apply for this fantastic opportunity.
New FP expansion team will be responsible for the global approach for the FP expansion projects across IFP and support a standardized design and requirement setup for all new FP lines.
The position
You will be part of a newly establish team, with the responsibilities of setting direction, approving documentation and keep oversight in relation to validation of all new FP lines across IFP. The team have the responsibility of QA review and oversight of several types of documents related to validation and qualification, to ensure product quality and compliance with the current GMP rules and guidelines.
You will have a role as Q-lead for one or more projects, where you will work closely together with several stakeholders across the world within DMD (Device Manufacturing Development), IFP and IFPQA, to ensure implementation of all new FP lines, with highest quality to patient in mind.
On top of that QA is a major player at internal audits and external authority inspections where you are expected to participate and present data when needed.
We can offer you a lot of freedom in planning your daily tasks, as well as occasionally working from home, when it fits into the operation and your peers in the team.
Qualifications
You hold a Master’s degree in engineering, pharmacy or similar and have solid experience within the pharmaceutical industry. You are able to set a clear direction, with reliable argumentation. Huge experience with quality assurance and/or production will be an advantage together with the right quality mindset.
You are ambitious and ready to be part of improving our high standards. 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. You are a dedicated team player who inspires trust and respect amongst colleagues and stakeholders. We are cooperating broadly with many stakeholders and therefore excellent collaboration and communication skills are needed.
We operate in an international company and the position therefore requires proficiency in English.
About the department
Our Quality assurance department consist of 25 dedicated employees, and we are still growing and soon we will be 30 employees. Our department is responsible for assuring quality and compliance of FP operations and support the business by improving and simplifying processes. Our department releases life saving Novo Nordisk products to our patients every day and we have a strong cooperation with our stakeholders to make this happen.
We are looking into a future where new production lines need to be implemented, to help Novo Nordisk succeed with the rising demand of our products from our patients. In order to succeed, this requires a Quality department with a high level of commitment to ensure highest quality to our patient, even when we are challenged during project execution and daily operation.
Working at Novo Nordisk
At Novo Nordisk, your skills, dedication, and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.
Contact
For further information, please contact Mette Lise Christensen +45 30752664.
Deadline
20th of January 2023.
Applications will be screened on an ongoing basis, so you are encouraged to apply as soon as possible.
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 23.12.2022, 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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