Senior Equipment Engineer Environmental Monitoring
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Gentofte
Are you passionate about highly specialised measurement equipment and pharmaceutical production? Are you interested in joining a dynamic team working at the forefront of modern technology where you can make a difference by bringing your technical skills into play? Then apply today for a life-changing career! The position
The overall objective is to be the future technical anchor for environmental monitoring systems in Aseptic Production (AP) worldwide. As the first in the industry, we have recently introduced a new technology for monitoring air cleanliness by use of laser-based bio-fluorescent particle counters for strict monitoring of particles and viable microorganisms in the AP production facilities. You will join a team of experts and specialists covering all aspects of the AP processes across Biotech & Rare Disease (BRD) and other SVP areas in Product Supply, including the requirements to establish, operate, and maintain facilities and environment used for manufacturing. Main responsibilities:
• Act as central expert on the roll out of this new technology, supporting our production sites with implementation, use and maintenance knowledge
• Facilitate knowledge sharing across our international production sites
• Be key in troubleshooting in case of unforeseen issues or equipment break-down and you will be the bridge between supplier and users
• Be on top of the newest hardware and software updates to the equipment and you will set the company direction on update and maintenance strategy
Qualifications
To succeed in this position, you have:
• An engineering degree or similar or have obtained extensive knowledge about measuring technologies and calibration of instruments.
• At least +5 years’ experience working with maintenance or specialised measurement equipment in highly regulated environments
• The ability to acquire the needed in depth knowledge of equipment technology and functionality, and are skilled in the integration of measurement systems in IT structures
• Knowledge of relevant international standards related to particle monitoring e.g. ISO and other relevant guidelines
• Scientific curiosity to deep dive into details and then put the pieces together to form a broader picture
• Fully proficient in both written and spoken English, while Danish is an advantage Apart from this, AP experience, clean room knowledge, and general GMP knowledge are all considered great plusses. As you will be collaborating with a wide range of stakeholders, including the equipment owners on the production sites across Product Supply, as well as external partners, strong communication and interpersonal skills are key. About the department
Manufacturing Development is a part of BRD with a team of over 650 colleagues working together to optimise and develop processes across six global production sites. Our field of work broadly covers the area also known as MSAT (Manufacturing, Science, and Technology). We bring value to our patients by driving innovation for the entire BRD, working with Industry 4.0, new technologies, biotechnology, and developing processes for both existing and future products. Working at Novo Nordisk
BRD is part of Novo Nordisk Product Supply, which is a global production network at the forefront of technology and quality production of pharmaceutical products. In BRD, we are not only supplying all Novo Nordisk products to people living with serious chronic diseases, but we also use our competences in biotech to support the growing efforts into completely new production platforms and therapy areas for Novo Nordisk.
We are more than 3000 dedicated colleagues working at six production sites in Denmark and the United States. Here we cover the entire production value chain where raw materials are cultivated, purified, formulated, filled, assembled in devices, packed, and distributed across the globe. As more and more people need our products, we support Novo Nordisk's initiatives in new therapy areas. Every day, we work to streamline and expand our capacity through process innovation, automation, and the introduction of new technology. Contact
For further information, please contact Mette Virklund, Specialist +45 30758169. Deadline
4 January 2024.
Please be advised the interviews will be conducted on an ongoing basis, so we encourage you to apply as soon as possible. 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.
The overall objective is to be the future technical anchor for environmental monitoring systems in Aseptic Production (AP) worldwide. As the first in the industry, we have recently introduced a new technology for monitoring air cleanliness by use of laser-based bio-fluorescent particle counters for strict monitoring of particles and viable microorganisms in the AP production facilities. You will join a team of experts and specialists covering all aspects of the AP processes across Biotech & Rare Disease (BRD) and other SVP areas in Product Supply, including the requirements to establish, operate, and maintain facilities and environment used for manufacturing. Main responsibilities:
• Act as central expert on the roll out of this new technology, supporting our production sites with implementation, use and maintenance knowledge
• Facilitate knowledge sharing across our international production sites
• Be key in troubleshooting in case of unforeseen issues or equipment break-down and you will be the bridge between supplier and users
• Be on top of the newest hardware and software updates to the equipment and you will set the company direction on update and maintenance strategy
Qualifications
To succeed in this position, you have:
• An engineering degree or similar or have obtained extensive knowledge about measuring technologies and calibration of instruments.
• At least +5 years’ experience working with maintenance or specialised measurement equipment in highly regulated environments
• The ability to acquire the needed in depth knowledge of equipment technology and functionality, and are skilled in the integration of measurement systems in IT structures
• Knowledge of relevant international standards related to particle monitoring e.g. ISO and other relevant guidelines
• Scientific curiosity to deep dive into details and then put the pieces together to form a broader picture
• Fully proficient in both written and spoken English, while Danish is an advantage Apart from this, AP experience, clean room knowledge, and general GMP knowledge are all considered great plusses. As you will be collaborating with a wide range of stakeholders, including the equipment owners on the production sites across Product Supply, as well as external partners, strong communication and interpersonal skills are key. About the department
Manufacturing Development is a part of BRD with a team of over 650 colleagues working together to optimise and develop processes across six global production sites. Our field of work broadly covers the area also known as MSAT (Manufacturing, Science, and Technology). We bring value to our patients by driving innovation for the entire BRD, working with Industry 4.0, new technologies, biotechnology, and developing processes for both existing and future products. Working at Novo Nordisk
BRD is part of Novo Nordisk Product Supply, which is a global production network at the forefront of technology and quality production of pharmaceutical products. In BRD, we are not only supplying all Novo Nordisk products to people living with serious chronic diseases, but we also use our competences in biotech to support the growing efforts into completely new production platforms and therapy areas for Novo Nordisk.
We are more than 3000 dedicated colleagues working at six production sites in Denmark and the United States. Here we cover the entire production value chain where raw materials are cultivated, purified, formulated, filled, assembled in devices, packed, and distributed across the globe. As more and more people need our products, we support Novo Nordisk's initiatives in new therapy areas. Every day, we work to streamline and expand our capacity through process innovation, automation, and the introduction of new technology. Contact
For further information, please contact Mette Virklund, Specialist +45 30758169. Deadline
4 January 2024.
Please be advised the interviews will be conducted on an ongoing basis, so we encourage you to apply as soon as possible. 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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Jobbet er oprettet på vores service den 19.9.2023, men kan have været deaktiveret og genaktiveret igen.
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