Senior Validation Engineer
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Hillerød
Are you passionate about validation processes? Do you have extensive experience in writing and reviewing validation documentation? We are looking for a dedicated Validation Engineer to join our team at Novo Nordisk, focusing on injection moulding tools and spare parts. If this sounds like you, read on and apply today for a life-changing career. The Position
As a Senior Validation Engineer, you will write and review validation plans, protocols, and reports associated with, among others, Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ). The main tasks will be to:
• Write and review validation plans, protocols, and reports associated with Installation Qualification, (IQ), Operational Qualification (OQ) and Performance Qualification (PQ).
• Drive each validation process by use of project management and by collaborating across the organisation with stakeholders from QA, Logistics, Production, Project Management and Production Support for both moulds and utilities.
• Write validation deviations and drive related problem solving.
• Assist Logistics and DCM Moulding Support in colour validations, variant validations, spare part validations etc. coordinating with production and logistics.
• Assist in and drive problem solving through systematic problem-solving tools, involving appropriate stakeholders.
• Participate in, and drive, planning activities with stakeholders across multiple areas.
You will provide updates on board meetings on the status of validation activities and ensure close collaboration with production on running validations. Participate in relevant board meetings in production when necessary. Qualifications To succeed in this role, you have:
• An academical background mechanical engineering or similar.
• Extensive experience in validation processes and documentation.
• Experience in injection moulding machines and verification.
• GMP experience.
• Excellent communication skills in Danish and English. As a person you have good interpersonal skills, you are process oriented and can communicate in a simple way. It is also important you support the rest of the team in creating a positive spirit and a good department. You are a team player, leading by going in front and solution oriented. About the Department Being a part of Novo Nordisk's Device Component Production (DCP) means working with a focus at one of the world's largest and most successful pharmaceutical companies. Our DCP organisation is responsible for manufacturing and sourcing of devices and device components and as such plays a vital part of Novo Nordisk's delivery to our patients.
You will join our Project and Data Execution team at site Hillerød, a diverse team solving a multitude of tasks across the organisation - ranging from Validation and Verification of moulds and associated spare parts, across designing and deploying reporting and knowledge sharing solutions to participating in, and run, small and large projects.
Working at Novo Nordisk We are a proud life-science company, and life is our reason to exist. We’re inspired by life in all its forms and shapes, ups and downs, opportunities and challenges. For employees at Novo Nordisk, life means many things – from the building blocks of life that form the basis of ground-breaking scientific research, to our rich personal lives that motivate and energise us to perform our best at work. Ultimately, life is why we’re all here - to ensure that people can lead a life independent of chronic disease. Contact For further information, please contact Manager Peter Morrud at +. Deadline Apply before January, 6 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 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.
As a Senior Validation Engineer, you will write and review validation plans, protocols, and reports associated with, among others, Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ). The main tasks will be to:
• Write and review validation plans, protocols, and reports associated with Installation Qualification, (IQ), Operational Qualification (OQ) and Performance Qualification (PQ).
• Drive each validation process by use of project management and by collaborating across the organisation with stakeholders from QA, Logistics, Production, Project Management and Production Support for both moulds and utilities.
• Write validation deviations and drive related problem solving.
• Assist Logistics and DCM Moulding Support in colour validations, variant validations, spare part validations etc. coordinating with production and logistics.
• Assist in and drive problem solving through systematic problem-solving tools, involving appropriate stakeholders.
• Participate in, and drive, planning activities with stakeholders across multiple areas.
You will provide updates on board meetings on the status of validation activities and ensure close collaboration with production on running validations. Participate in relevant board meetings in production when necessary. Qualifications To succeed in this role, you have:
• An academical background mechanical engineering or similar.
• Extensive experience in validation processes and documentation.
• Experience in injection moulding machines and verification.
• GMP experience.
• Excellent communication skills in Danish and English. As a person you have good interpersonal skills, you are process oriented and can communicate in a simple way. It is also important you support the rest of the team in creating a positive spirit and a good department. You are a team player, leading by going in front and solution oriented. About the Department Being a part of Novo Nordisk's Device Component Production (DCP) means working with a focus at one of the world's largest and most successful pharmaceutical companies. Our DCP organisation is responsible for manufacturing and sourcing of devices and device components and as such plays a vital part of Novo Nordisk's delivery to our patients.
You will join our Project and Data Execution team at site Hillerød, a diverse team solving a multitude of tasks across the organisation - ranging from Validation and Verification of moulds and associated spare parts, across designing and deploying reporting and knowledge sharing solutions to participating in, and run, small and large projects.
Working at Novo Nordisk We are a proud life-science company, and life is our reason to exist. We’re inspired by life in all its forms and shapes, ups and downs, opportunities and challenges. For employees at Novo Nordisk, life means many things – from the building blocks of life that form the basis of ground-breaking scientific research, to our rich personal lives that motivate and energise us to perform our best at work. Ultimately, life is why we’re all here - to ensure that people can lead a life independent of chronic disease. Contact For further information, please contact Manager Peter Morrud at +. Deadline Apply before January, 6 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 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 Hillerød.
Jobbet er oprettet på vores service den 16.12.2024, 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
- Hillerød
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| Dato | Alle jobs som øvrige |
|---|---|
| 18. januar 2025 | 71 |
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