QC Supporter for Device Laboratory
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Hillerød
We are looking to expand the team with a dedicated Quality Control Supporter with an interest in testing of medical devices.
Do you enjoy working with LIMS, Stability Studies and Device tests? Would you like to play a key role in the important mission to ensure that people living with chronical diseases can always rely on Novo Nordisk products to be safe and effective? Then we look forward to your application and to potentially welcoming you as our new colleague in Device Manufacturing Development (DMD) in Hillerød.
About the department
Who is the team waiting for you?
Our team ‘QC Release and Stability Testing’ is part of Device Manufacturing Development (DMD), where we are responsible for the device stability on Drug Device Combinations products and QC release test on new products before they are introduced to the market. Your new colleagues will be 5 laboratory technicians and one stability professional, all excited to welcome and share knowledge with you.
We operate in a diverse landscape of stakeholders, balancing many concerns in a complex, international business environment, and we never compromise on the quality of our work. We share an informal tone, great work morale and tall ambitions to be the best at what we do.
The position
Together with your team, you will oversee the device testing and quality control processes for new and existing products. You will mainly be working with device stability and device release tests; dosage accuracy, dose force and tests of mechanical and physical properties of various electronic components and devices.
We work with a range of advanced test equipment, and here you will have the opportunity to build your knowledge about state-of-the art test technology like cobots, as our aim is to be ahead of regulative standards and build our position in a growing market. Sustainably is high up on our agenda, which is why we strive to work paperless in our laboratories, hence LIMS and other digital platforms is a large part of our daily work.
As QC supporter in ‘Release and Stability Testing’ your task will, among others, be:
Some of your softer skills, such as your collaborative and communicative competencies, will inevitably also get stronger. This is due to you working with colleagues across and beyond a diverse organisation.
Qualifications
It is important that you approach your work with an openminded and positive attitude, want to make a difference and are eager to learn.
You like to collaborate around exciting challenges, with a sense of urgency and strict quality standards. You are known as someone who can meet deadlines with a structured approach and keep the overview – even in a busy environment where priorities can change quickly. It will have the ability to work and deliver results independently and at the same time be a team player who shines together with your colleagues.
We expect you to be fluent in both Danish and English, both verbally and in writing.
Working at Novo Nordisk
In Novo Nordisk, you will be met with trust and exciting professional challenges. You will have the opportunity to work with dedicated colleagues, who strive every day to deliver perfection to the many people living with chronical diseases using our devices. We are proud to make a difference and look forward to welcoming you here.
You can learn more about working at Novo Nordisk here: http://www.novonordisk.com/careers/working-at-novo-nordisk.html
Contact
Should you have questions about the position, you are welcome to call Tina Povlsen at +45 3079 1569 or by mail [email protected]
Deadline
January 8th 2023
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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Do you enjoy working with LIMS, Stability Studies and Device tests? Would you like to play a key role in the important mission to ensure that people living with chronical diseases can always rely on Novo Nordisk products to be safe and effective? Then we look forward to your application and to potentially welcoming you as our new colleague in Device Manufacturing Development (DMD) in Hillerød.
About the department
Who is the team waiting for you?
Our team ‘QC Release and Stability Testing’ is part of Device Manufacturing Development (DMD), where we are responsible for the device stability on Drug Device Combinations products and QC release test on new products before they are introduced to the market. Your new colleagues will be 5 laboratory technicians and one stability professional, all excited to welcome and share knowledge with you.
We operate in a diverse landscape of stakeholders, balancing many concerns in a complex, international business environment, and we never compromise on the quality of our work. We share an informal tone, great work morale and tall ambitions to be the best at what we do.
The position
Together with your team, you will oversee the device testing and quality control processes for new and existing products. You will mainly be working with device stability and device release tests; dosage accuracy, dose force and tests of mechanical and physical properties of various electronic components and devices.
We work with a range of advanced test equipment, and here you will have the opportunity to build your knowledge about state-of-the art test technology like cobots, as our aim is to be ahead of regulative standards and build our position in a growing market. Sustainably is high up on our agenda, which is why we strive to work paperless in our laboratories, hence LIMS and other digital platforms is a large part of our daily work.
As QC supporter in ‘Release and Stability Testing’ your task will, among others, be:
- Laboratory Support
- Local Test Method responsible
- Deviation handling
- Laboratory Investigations (LI’s)
- Review and verification of test methods (LIMS)
- Handling of laboratory procedures and SOP’s.
- Drive local improvement projects.
Some of your softer skills, such as your collaborative and communicative competencies, will inevitably also get stronger. This is due to you working with colleagues across and beyond a diverse organisation.
Qualifications
- You hold at least a bachelor’s degree within engineering, Medicine and technology, pharmacy, chemistry or similar
- Experience from laboratory activities preferably in the pharmaceutical or Medical Device industry and have worked with quality processes
- You are ambitious and ready to take on the responsibility in building strong competencies in our team and trustful relations across the organisation
- You can use your excellent cooperation skills when you manage your stakeholders to ensure solutions that will meet both requirements and stakeholder’s interests
- You are well-organised and have a flexible, but firm approach when making decisions
- It is an advantage but not a requirement, that you have worked with medical devices and combination product, as well as has experienced with interpretation of relevant regulatory requirements and standards
- Knowledge and possible experience with LIMS and GMP in QC-laboratories, in a regulated laboratory environment, is also considered as an advantage
It is important that you approach your work with an openminded and positive attitude, want to make a difference and are eager to learn.
You like to collaborate around exciting challenges, with a sense of urgency and strict quality standards. You are known as someone who can meet deadlines with a structured approach and keep the overview – even in a busy environment where priorities can change quickly. It will have the ability to work and deliver results independently and at the same time be a team player who shines together with your colleagues.
We expect you to be fluent in both Danish and English, both verbally and in writing.
Working at Novo Nordisk
In Novo Nordisk, you will be met with trust and exciting professional challenges. You will have the opportunity to work with dedicated colleagues, who strive every day to deliver perfection to the many people living with chronical diseases using our devices. We are proud to make a difference and look forward to welcoming you here.
You can learn more about working at Novo Nordisk here: http://www.novonordisk.com/careers/working-at-novo-nordisk.html
Contact
Should you have questions about the position, you are welcome to call Tina Povlsen at +45 3079 1569 or by mail [email protected]
Deadline
January 8th 2023
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 Hillerød.
Jobbet er oprettet på vores service den 8.7.2022, 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
- Hillerød
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Statistik over udbudte øvrige i Hillerød over tid
| Dato | Alle jobs som øvrige |
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