Project Engineer to Automation
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Are you eager implement and maintain independent automation resolution? Would you like to work in one of the best IT organizations in the pharmaceutical industry? Then you might be our new Project Engineer to Automation. Apply today and join our team! About the department
You will join our technical support team of 11 dedicated engineers and technicians who daily ensure that our 8 highly automated assembly and packaging lines run optimally, and that we always work according to the applicable requirements. Innovation is a part of our mindset, and we are looking for technologies to meet our vision of bringing lights out into a finished product facility. The position
As Project Engineer to Automation you will be responsible for operational support. You will use of cLEAN in error detection and improvement of operations, including use of standardised tools such as A3 and 3C. You will also support the daily operation in the assembly and packaging lines and advice regarding larger improvements on the lines. Your responsibility will be development of technical inputs to deviations, understanding and maintaing the relation between qualification documentation and the equipment in the department. You will develop qualification documentation, IV and OV. You will work on executing of qualification activities including configuration control, data review, CR handling and updating requirement documentation, requirement specifications and risk analysis. You will permanently and continuously handle maintenance of the qualified state on the department’s production plant through the preparation of OPV/SE (Ongoing Process Verification) and URR (User access Review Report). You will prepare new workflows and optimise existing through innovation and cLEAN and ensure ownership and involvement of the stakeholders (operators/skilled workers etc.). You will participate in the development and implementation of automation projects supporting the department’s ambition of Lights Out. To sum up, your main responsibility will be to:
• Ensure compliance and operational stability of equipment through independent management of projects and tasks.
• Participate in optimization and error correction.
• Ensure the use and retaining of cLEAN activities in the department.
• Drive and coordinate CR-cases and validation tasks.
Qualifications
To succeed in this position, we expect you:
• hold a BSc or MSc degree in Engineering
• have quality understanding
• have experience with GMP, ISO 9001
• have experience with highly automated equipment. As a person, you have good collaboration and communication skills. You challenge existing solutions and initiate new actions and you are responsible, organised and systematic. You are outgoing and able to collaborate and communicate with many different professional fields and backgrounds. You are also able to determined and you are good at keeping deadlines. You are impactful and power of action. You like to take initiative. You are independent and good at planning own work and give/receive feedback. Working at Novo Nordisk
Novo Nordisk is its people. We know that life is anything but linear, and balancing what is important at different stages of our career is never easy. That’s why we make room for diverse life situations, always putting people first. We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 57,000 employees. Together, we go further. Together, we’re life changing. Contact
For further information, please contact Lars Solgaard, Associate manager at +4530754945. Deadline
10 November 2023. Please note that applications will be reviewed on an ongoing basis, so we encourage you to apply as soon as possible. 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.
You will join our technical support team of 11 dedicated engineers and technicians who daily ensure that our 8 highly automated assembly and packaging lines run optimally, and that we always work according to the applicable requirements. Innovation is a part of our mindset, and we are looking for technologies to meet our vision of bringing lights out into a finished product facility. The position
As Project Engineer to Automation you will be responsible for operational support. You will use of cLEAN in error detection and improvement of operations, including use of standardised tools such as A3 and 3C. You will also support the daily operation in the assembly and packaging lines and advice regarding larger improvements on the lines. Your responsibility will be development of technical inputs to deviations, understanding and maintaing the relation between qualification documentation and the equipment in the department. You will develop qualification documentation, IV and OV. You will work on executing of qualification activities including configuration control, data review, CR handling and updating requirement documentation, requirement specifications and risk analysis. You will permanently and continuously handle maintenance of the qualified state on the department’s production plant through the preparation of OPV/SE (Ongoing Process Verification) and URR (User access Review Report). You will prepare new workflows and optimise existing through innovation and cLEAN and ensure ownership and involvement of the stakeholders (operators/skilled workers etc.). You will participate in the development and implementation of automation projects supporting the department’s ambition of Lights Out. To sum up, your main responsibility will be to:
• Ensure compliance and operational stability of equipment through independent management of projects and tasks.
• Participate in optimization and error correction.
• Ensure the use and retaining of cLEAN activities in the department.
• Drive and coordinate CR-cases and validation tasks.
Qualifications
To succeed in this position, we expect you:
• hold a BSc or MSc degree in Engineering
• have quality understanding
• have experience with GMP, ISO 9001
• have experience with highly automated equipment. As a person, you have good collaboration and communication skills. You challenge existing solutions and initiate new actions and you are responsible, organised and systematic. You are outgoing and able to collaborate and communicate with many different professional fields and backgrounds. You are also able to determined and you are good at keeping deadlines. You are impactful and power of action. You like to take initiative. You are independent and good at planning own work and give/receive feedback. Working at Novo Nordisk
Novo Nordisk is its people. We know that life is anything but linear, and balancing what is important at different stages of our career is never easy. That’s why we make room for diverse life situations, always putting people first. We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 57,000 employees. Together, we go further. Together, we’re life changing. Contact
For further information, please contact Lars Solgaard, Associate manager at +4530754945. Deadline
10 November 2023. Please note that applications will be reviewed on an ongoing basis, so we encourage you to apply as soon as possible. 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 Måløv.
Jobbet er oprettet på vores service den 20.10.2023, 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
- Måløv
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