Engineering/Operations Responsible for Process Analytical Technology
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Kalundborg
Are you passionate about utilizing cutting-edge technology in pharmaceutical manufacturing? Do you have a “can do”-attitude, a strong background in downstream large-scale production and a keen interest in optimizing daily process control through introduction of NIR, LC and/or other Process Analytical Technology? If this describes you, we have an exciting opportunity that may be of interest!
The Position As our Engineering/Operation Responsible (ER/OR), you will play a pivotal role in ensuring the successful implementation and ongoing control of cutting-edge in-line/on-line and at-line analytical systems for real-time process monitoring, control, and optimization within our operations. Your responsibilities will be:
• Lead and oversee the implementation and ongoing control of on-line and in-line/at-line PAT instruments within our operations, ensuring they are ready for seamless integration.
• Troubleshoot and problem-solve issues that may arise during implementation and operations, providing vital support to maintain the efficiency and reliability of our processes.
• While anchored in process support, act as the PAT responsible, ensuring that PAT is always in control during operations
• Plan and document validation activities according to regulatory and internal Novo Nordisk requirements.
• Ensure SOPs and training are up to date. This role offers an exceptional opportunity for personal and professional growth. Your contributions will directly impact the success of our new facility, ultimately making a meaningful difference for patients. You will work in a dynamic, international environment, collaborating with diverse teams and leveraging innovative solutions to drive implementation. Qualifications To succeed in this role, you have:
• Strong technical background in chemical engineering, biotechnology, pharmacy, or related fields.
• Experience with in-line/on-line/at-line analytical techniques such as spectroscopy (NIR, UV, IR, Raman), chromatography (GC, LC), or similar methods.
• Familiarity with process control and pharmaceutical downstream processing.
• Understanding of method automation with PAT management system and DCS integration will be considered an advantage.
• Experience in the developing and validating analytical methods and equipment, particularly in the context of Science-risk based validation (SRV), will be advantageous. As a person, you enjoy working with different stakeholders and collaborate with cross-functional teams to define, assess, and document activities, ensuring the reliability for measurements of product attributes in real-time. Your efforts will revolutionize and elevate the efficiency and quality of our protein purification production process, paving the way for a new course in the future process monitoring paradigms. About the Department We are a rapidly growing team dedicated to making our new facility a reality. Our energetic and collaborative environment fosters creativity and innovation. Join us and be a part of our journey to shape the future of pharmaceutical production. If you are an innovative, solution-oriented professional with a passion for cutting-edge technology and a desire to make a real impact, we want to hear from you. Join us and be at the forefront of driving pharmaceutical manufacturing into the future! 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 Palle Møller Kristensen at +45-30750640.
Deadline Apply before December, 8 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.
The Position As our Engineering/Operation Responsible (ER/OR), you will play a pivotal role in ensuring the successful implementation and ongoing control of cutting-edge in-line/on-line and at-line analytical systems for real-time process monitoring, control, and optimization within our operations. Your responsibilities will be:
• Lead and oversee the implementation and ongoing control of on-line and in-line/at-line PAT instruments within our operations, ensuring they are ready for seamless integration.
• Troubleshoot and problem-solve issues that may arise during implementation and operations, providing vital support to maintain the efficiency and reliability of our processes.
• While anchored in process support, act as the PAT responsible, ensuring that PAT is always in control during operations
• Plan and document validation activities according to regulatory and internal Novo Nordisk requirements.
• Ensure SOPs and training are up to date. This role offers an exceptional opportunity for personal and professional growth. Your contributions will directly impact the success of our new facility, ultimately making a meaningful difference for patients. You will work in a dynamic, international environment, collaborating with diverse teams and leveraging innovative solutions to drive implementation. Qualifications To succeed in this role, you have:
• Strong technical background in chemical engineering, biotechnology, pharmacy, or related fields.
• Experience with in-line/on-line/at-line analytical techniques such as spectroscopy (NIR, UV, IR, Raman), chromatography (GC, LC), or similar methods.
• Familiarity with process control and pharmaceutical downstream processing.
• Understanding of method automation with PAT management system and DCS integration will be considered an advantage.
• Experience in the developing and validating analytical methods and equipment, particularly in the context of Science-risk based validation (SRV), will be advantageous. As a person, you enjoy working with different stakeholders and collaborate with cross-functional teams to define, assess, and document activities, ensuring the reliability for measurements of product attributes in real-time. Your efforts will revolutionize and elevate the efficiency and quality of our protein purification production process, paving the way for a new course in the future process monitoring paradigms. About the Department We are a rapidly growing team dedicated to making our new facility a reality. Our energetic and collaborative environment fosters creativity and innovation. Join us and be a part of our journey to shape the future of pharmaceutical production. If you are an innovative, solution-oriented professional with a passion for cutting-edge technology and a desire to make a real impact, we want to hear from you. Join us and be at the forefront of driving pharmaceutical manufacturing into the future! 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 Palle Møller Kristensen at +45-30750640.
Deadline Apply before December, 8 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 Kalundborg.
Jobbet er oprettet på vores service den 4.12.2024, 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
- Kalundborg
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