QA Professional for Device Manufacturing
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Hillerød
Are you looking for an exciting job opportunity in quality assurance? Do you want to play a vital part in the delivery of
The position
As a QA Professional in DCM QA you will become part of a great team of experienced and engaged QA professionals supporting the production of components and pre-assembly of the finished products as well as Quality Control and Metrology. Alongside the rest of the team, you will have the responsibility of QA review and over-sight of many types of documents, such as deviation, change request and valida-tion. Your main tasks include: Bring expert support to projects and validation activities Responsible QA for the molding and pre-assembly processes including QA oversight in the production facility Support to deviation handling as well as change requests for the area Furthermore, you will ensure quality and compliance with the current GMP rules and guidelines. As a team, we value a great working environment, team spirit and empowerment as well as good development opportunities.
Qualifications
To succeed in this role, you: Hold a master’s degree within engineering, life sciences or similar Preferably have some years of experience in QA related roles, but we are en-couraging newly graduates to apply as we Are proficient in English and Danish As a person you are ambitious and ready to be part of our on-going effort to improve our high standards. You dare to challenge us in our way of working and has the desire to take initiative as well as being responsible for your own learning. A proactive mind-set is key to succeeding in this role. You are an honest and dedicated team player who inspires and builds trust and re-spect amongst colleagues and partners. We are cooperating broadly with many stake-holders and therefore excellent collaboration and communication skills are needed.
About the department
You will join a highly dynamic and well-functioning department in DCM QA with many interfaces and stakeholders around the organization. The department consists of two teams who are supporting the production of device components (molding and pre-assembly), QC, metrology and more. The department have a high level of self-governance, and the working relations are informal. We value good humor and an open and honest culture.
Working at
At , we don't wait for change. We drive it. We're a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We are anchored on sci-entific innovation through the power of our diverse differences. We embrace the spirit of experimentation and strive for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and develop-ment, through to manufacturing, marketing, and sales – we are all working together to advance patient care.
Contact
If you want to know more about the position, please contact Quality Manager Navina Thangarajah at + .
Deadline
15 November 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.
’s high-quality products to our pa-tients? Are you an ambitious and proactive team player who sees collaboration as key to success? Then you might be the colleague we are missing in our Department of Device Compo-nent Manufacturing (DCM) Operations QA, read more and apply now! The position
As a QA Professional in DCM QA you will become part of a great team of experienced and engaged QA professionals supporting the production of components and pre-assembly of the finished products as well as Quality Control and Metrology. Alongside the rest of the team, you will have the responsibility of QA review and over-sight of many types of documents, such as deviation, change request and valida-tion. Your main tasks include:
Qualifications
To succeed in this role, you:
About the department
You will join a highly dynamic and well-functioning department in DCM QA with many interfaces and stakeholders around the organization. The department consists of two teams who are supporting the production of device components (molding and pre-assembly), QC, metrology and more. The department have a high level of self-governance, and the working relations are informal. We value good humor and an open and honest culture.
Working at
At , we don't wait for change. We drive it. We're a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We are anchored on sci-entific innovation through the power of our diverse differences. We embrace the spirit of experimentation and strive for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and develop-ment, through to manufacturing, marketing, and sales – we are all working together to advance patient care.
Contact
If you want to know more about the position, please contact Quality Manager Navina Thangarajah at + .
Deadline
15 November 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 8.11.2024, 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.
- 08.11.2024
- Øvrige
- Hillerød
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