Clean Utility Supporter
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Gentofte
Do you have a strong quality mindset and interested in clean utility and cooling facilities? Do you enjoy a job with a wide range of tasks where problem solving, and optimization is central in the daily business? If yes, then you might be our new colleague, we are looking for in Team Utility GMP & Validation Support.
The position
As a Utility Supporter you will have a wide range of diverse tasks, all ensuring our production is released according to all standards and requirements from the authorities. In team Utility GMP & Validation Support we aim to develop and optimise the way we work, and you will be part of optimise processes, and expand capacity of our process facilities using new technologies and innovative approaches.
Your key responsibilities will be:
This job holds a range of professional opportunities to develop expertise in a complex manufacturing setup where ambitions are high. We are great at supporting each other, making sure no one is left alone with more significant challenges when things get busy.
Qualifications
As a person, you have strong analytical skills, are structured and proactive in your work and will never compromise on quality. You appreciate the value of accurate and timely documentation as the essential safety and quality control parameter it is. To succeed you need to be able to work independently and keep a calm and be able to make decisions in a busy work environment where the agenda changes frequently. It is paramount for this position that you are fluent in Danish as well as in English, making it easy for you to facilitate and contribute to technical discussions.
About the department
Biotech Rare Disease Finished Products Gentofte/Værløse (BRD FP GEVA) Technical Service is a technical department with app. 60 employees delivering technical services and releasing various utilities to departments across site Gentofte and Værløse. The department is responsible for delivering Water for Injection (WFI), clean steam, compressed air, various gases, cooling, ventilation and support to projects and daily operation. The department is structured in 4 teams with each their area of responsibility. You will be part of team Utility GMP & Validation Support consisting of 12 colleagues with different educational backgrounds.
Working at Novo Nordisk
At Novo Nordisk, 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 embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care.
Contact
If you have questions about the position, please call Frederikke Hall at +45 30776046.
Deadline
December 12th 2022
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.
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The position
As a Utility Supporter you will have a wide range of diverse tasks, all ensuring our production is released according to all standards and requirements from the authorities. In team Utility GMP & Validation Support we aim to develop and optimise the way we work, and you will be part of optimise processes, and expand capacity of our process facilities using new technologies and innovative approaches.
Your key responsibilities will be:
- Qualification, verification, and heat studies of cooling facilities.
- Trend monitoring, data extractions, deviation handling, change requests and reporting
- Participate in different projects in the team.
- Update of instructions and Standard Operating Procedures (SOP) securing they are up to date and ready to meet current GMP requirements.
- It is an advantage if you have experience with writing SOP’s, Change Requests and maybe systematic problem solving in relation to working with deviations within the pharmaceutical industry.
This job holds a range of professional opportunities to develop expertise in a complex manufacturing setup where ambitions are high. We are great at supporting each other, making sure no one is left alone with more significant challenges when things get busy.
Qualifications
- You have a pragmatic and it-can-be-done approach to your tasks.
- We imagine that you have a degree within pharmacy, chemistry/biology or engineering, and you preferably have a couple years of experience working with cooling facilities in the pharmaceutical or food industry under GMP regulation.
- You are interested in new technologies and how to implement them to optimize our processes. You are systematic and have a structured way of working with your tasks.
- You have a positive attitude, a proactive behavior, and gain energy by working in close collaboration with your team colleagues and other stakeholders.
As a person, you have strong analytical skills, are structured and proactive in your work and will never compromise on quality. You appreciate the value of accurate and timely documentation as the essential safety and quality control parameter it is. To succeed you need to be able to work independently and keep a calm and be able to make decisions in a busy work environment where the agenda changes frequently. It is paramount for this position that you are fluent in Danish as well as in English, making it easy for you to facilitate and contribute to technical discussions.
About the department
Biotech Rare Disease Finished Products Gentofte/Værløse (BRD FP GEVA) Technical Service is a technical department with app. 60 employees delivering technical services and releasing various utilities to departments across site Gentofte and Værløse. The department is responsible for delivering Water for Injection (WFI), clean steam, compressed air, various gases, cooling, ventilation and support to projects and daily operation. The department is structured in 4 teams with each their area of responsibility. You will be part of team Utility GMP & Validation Support consisting of 12 colleagues with different educational backgrounds.
Working at Novo Nordisk
At Novo Nordisk, 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 embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care.
Contact
If you have questions about the position, please call Frederikke Hall at +45 30776046.
Deadline
December 12th 2022
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.
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Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Gentofte.
Jobbet er oprettet på vores service den 22.11.2022, 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
- Gentofte
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Statistik over udbudte øvrige i Gentofte over tid
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