QA Professional in Validation
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Hillerød
Are you interested in growing your career in QA? Are you ready to take on a challenging role as the QA Professional at ? If you are looking for an opportunity to make a significant impact, then apply today for a life-changing career! The Position
In close collaboration with your colleagues, you will identify and contribute to the strengthening of our stakeholders’ compliance and Quality level. You will be responsible for verifying the quality of our Finished Products production, which can include:
• Working with and reviewing Deviations to ensure production complies with the current requirements, creating the right strategy, and implementing sufficient actions
• Reviewing change requests and approving all changes wanted by production
• Reviewing and approving SOP updates
• Being quality responsible for validation projects. In this role you will be part of driving optimizations either between QA and production or locally in QA. Qualifications
To succeed in this role, the most important thing is that you find energy in balancing different tasks such as: handling daily routine tasks and larger projects which contribute positively to the well-being and balance of the team. You will join a production site with a high pace, which mean you must be motivated by flexible workstyle and ability to prioritize your own tasks and time. We expect the successful candidate to have:
• An academic degree within Pharmacy, Engineering, Master of Science or equivalent
• Work experience in QA or GMP production together with the right quality mindset
• A structured approach to your work and always see your tasks through
• A strong sense of quality, are ambitious and ready to be part of our on-going efforts to improve our high standards
• Fluency in English, both written and spoken. As a person you dare to challenge us in our way of working and have a desire to take initiative as well as being responsible for your own learning. About the Department
The team is responsible for ensuring the best quality and compliance level in our production of Finished Product (FP) by supporting the patients needs by constantly improving the processes. You will be part of a team consisting of 16 dedicated colleagues who are proud of the inclusive work environment we have built, and who share an interest in creating ambitious results through collaboration and curiosity. The team consist of both very experienced colleagues (+20 years) and newly educated individuals. We focus on good social relations and prioritize to make room for fun at work. We have weekly workout sessions and cake eating to ensure on-going well-being in the team. We are part of both the deviation reduction journey, and changes that improve the production lines and processes. Furthermore, we are also a main resource in the new FP expansion process where 4 new lines will be installed over the next 3 years. Working at
is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy within diabetes, we are growing massively and expanding our commitment, reaching millions around the world and impacting more than 40 million patient lives daily. All of this has made us one of the 20 most valuable companies in the world by market cap. Our success relies on the joint potential and collaboration of our more than 63,000 employees around the world. We recognize the importance of the unique skills and perspectives our people bring to the table, and we work continuously to bring out the best in them. Working at , we’re working toward something bigger than ourselves, and it’s a collective effort. Join us! Together, we go further. Together, we’re life changing. Contact
For further information, please contact Associate Manager, Christian Klibo Buur on +or via e-mail at Deadline
12 May 2024. 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 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.
In close collaboration with your colleagues, you will identify and contribute to the strengthening of our stakeholders’ compliance and Quality level. You will be responsible for verifying the quality of our Finished Products production, which can include:
• Working with and reviewing Deviations to ensure production complies with the current requirements, creating the right strategy, and implementing sufficient actions
• Reviewing change requests and approving all changes wanted by production
• Reviewing and approving SOP updates
• Being quality responsible for validation projects. In this role you will be part of driving optimizations either between QA and production or locally in QA. Qualifications
To succeed in this role, the most important thing is that you find energy in balancing different tasks such as: handling daily routine tasks and larger projects which contribute positively to the well-being and balance of the team. You will join a production site with a high pace, which mean you must be motivated by flexible workstyle and ability to prioritize your own tasks and time. We expect the successful candidate to have:
• An academic degree within Pharmacy, Engineering, Master of Science or equivalent
• Work experience in QA or GMP production together with the right quality mindset
• A structured approach to your work and always see your tasks through
• A strong sense of quality, are ambitious and ready to be part of our on-going efforts to improve our high standards
• Fluency in English, both written and spoken. As a person you dare to challenge us in our way of working and have a desire to take initiative as well as being responsible for your own learning. About the Department
The team is responsible for ensuring the best quality and compliance level in our production of Finished Product (FP) by supporting the patients needs by constantly improving the processes. You will be part of a team consisting of 16 dedicated colleagues who are proud of the inclusive work environment we have built, and who share an interest in creating ambitious results through collaboration and curiosity. The team consist of both very experienced colleagues (+20 years) and newly educated individuals. We focus on good social relations and prioritize to make room for fun at work. We have weekly workout sessions and cake eating to ensure on-going well-being in the team. We are part of both the deviation reduction journey, and changes that improve the production lines and processes. Furthermore, we are also a main resource in the new FP expansion process where 4 new lines will be installed over the next 3 years. Working at
is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy within diabetes, we are growing massively and expanding our commitment, reaching millions around the world and impacting more than 40 million patient lives daily. All of this has made us one of the 20 most valuable companies in the world by market cap. Our success relies on the joint potential and collaboration of our more than 63,000 employees around the world. We recognize the importance of the unique skills and perspectives our people bring to the table, and we work continuously to bring out the best in them. Working at , we’re working toward something bigger than ourselves, and it’s a collective effort. Join us! Together, we go further. Together, we’re life changing. Contact
For further information, please contact Associate Manager, Christian Klibo Buur on +or via e-mail at Deadline
12 May 2024. 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 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 Hillerød.
Jobbet er oprettet på vores service den 29.4.2024, 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.
- 29.04.2024
- Øvrige
- Hillerød
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