Process Supporter
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Kalundborg
Do you have focus on or interest in data analysis, process systems and descriptive and prescriptive analytics? Would you like to bring your interest for understanding pharmaceutical and cleaning processes, develop monitoring tools and analyze data for recommendation for improvements? Are you interested in having true business impact and understanding how interconnected decisions play a crucial role in producing Active Pharmaceutical Ingredients (APIs)? Then you might be our new Process Supporter for API manufacturing in . Read on and apply today!
The Position As a Process Supporter, you will join on of the teams that has responsibility for cleaning validation and monitoring of the equipment in the department as well as monitoring the process. You might also be involved in product changeover, optimization projects and with time, be equipped to help cleaning and supporter colleagues across production facilities. There is a strong focus on LEAN-systems, which together with our quality mindset, drives continuous improvements across the department. Everything we do is regulated by Good Manufacturing Practice (GMP), and we must be aware of the challenges this creates. This position offers a great opportunity to play a part in shaping the future of bioprocessing across the organization, in close collaboration with teach-transfer and manufacturing in other departments across company. The main tasks will be:
• Support cleaning processes on a day-to-day basis and ensure smooth operation by optimizing current monitoring processes within regulatory requirements, and handle problem solving in a systematic manner to eliminate problems completely.
• Use a data-based approach for quantifying process/cleaning deviations.
• Analyse large amounts of data for extracting correlation and causation for process understanding.
• Develop and maintain statistical process control charts for process monitoring.
• Apply a team-based approach for recommending process improvements-optimizations. Qualifications To be considered for this position, you should have:
• A bachelor’s or master’s degree in in chemical, industrial or mechanical engineering, or similar field.
• Strong experience in similar positions in highly regulated industries, which is considered a plus.
• Ability to analyse data and independently extract information.
• Fluency in English, the ability to fluently use Danish or a will to learn Danish is considered a plus. On a personal level, you are both a team player and a professional who works independently. Having an appetite for solving complex problems applying a systems approach to manage complexity and reach feasible applicable solution is crucial in this role. Understanding of how to convey complex information to varying audiences and thereby, explaining the purpose to get everyone onboard is key to succeed in this role. About the department As part of ’s Product Supply organization, Diabetes Active Pharmaceutical Ingredients is responsible for manufacturing all Insulin-based products. You will be assigned to Insulin Manufacturing 1 (M1), the world’s largest Insulin API manufacturing facility located in Kalundborg. M1 has 5 facilities operating under one roof. You will be employed in Purification, with a team of skilled international colleagues all working together to ensure that API is purified and released. The department of Purification lies at the interface between Upstream manufacturing, where the initial API is generated and Product formulation where the API is formulated into the final product for the patient. Purification plays an important role in API manufacturing because it is responsible for generating the final API, purifying it to a high quality and ensuring that product is supplied to the next stage in the supply chain for access to the patient. Therefore, data analysis, process monitoring, dialogue with key stakeholders and recommendations for process improvements are crucial. Working at At , 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 For further information, please contact Manager Claes Tinglev Åside at +or Manager Troels Bundgaard Jensen at +. Deadline 6 September 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 a Process Supporter, you will join on of the teams that has responsibility for cleaning validation and monitoring of the equipment in the department as well as monitoring the process. You might also be involved in product changeover, optimization projects and with time, be equipped to help cleaning and supporter colleagues across production facilities. There is a strong focus on LEAN-systems, which together with our quality mindset, drives continuous improvements across the department. Everything we do is regulated by Good Manufacturing Practice (GMP), and we must be aware of the challenges this creates. This position offers a great opportunity to play a part in shaping the future of bioprocessing across the organization, in close collaboration with teach-transfer and manufacturing in other departments across company. The main tasks will be:
• Support cleaning processes on a day-to-day basis and ensure smooth operation by optimizing current monitoring processes within regulatory requirements, and handle problem solving in a systematic manner to eliminate problems completely.
• Use a data-based approach for quantifying process/cleaning deviations.
• Analyse large amounts of data for extracting correlation and causation for process understanding.
• Develop and maintain statistical process control charts for process monitoring.
• Apply a team-based approach for recommending process improvements-optimizations. Qualifications To be considered for this position, you should have:
• A bachelor’s or master’s degree in in chemical, industrial or mechanical engineering, or similar field.
• Strong experience in similar positions in highly regulated industries, which is considered a plus.
• Ability to analyse data and independently extract information.
• Fluency in English, the ability to fluently use Danish or a will to learn Danish is considered a plus. On a personal level, you are both a team player and a professional who works independently. Having an appetite for solving complex problems applying a systems approach to manage complexity and reach feasible applicable solution is crucial in this role. Understanding of how to convey complex information to varying audiences and thereby, explaining the purpose to get everyone onboard is key to succeed in this role. About the department As part of ’s Product Supply organization, Diabetes Active Pharmaceutical Ingredients is responsible for manufacturing all Insulin-based products. You will be assigned to Insulin Manufacturing 1 (M1), the world’s largest Insulin API manufacturing facility located in Kalundborg. M1 has 5 facilities operating under one roof. You will be employed in Purification, with a team of skilled international colleagues all working together to ensure that API is purified and released. The department of Purification lies at the interface between Upstream manufacturing, where the initial API is generated and Product formulation where the API is formulated into the final product for the patient. Purification plays an important role in API manufacturing because it is responsible for generating the final API, purifying it to a high quality and ensuring that product is supplied to the next stage in the supply chain for access to the patient. Therefore, data analysis, process monitoring, dialogue with key stakeholders and recommendations for process improvements are crucial. Working at At , 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 For further information, please contact Manager Claes Tinglev Åside at +or Manager Troels Bundgaard Jensen at +. Deadline 6 September 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 31.7.2024, 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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Statistik over udbudte øvrige i Kalundborg over tid
| Dato | Alle jobs som øvrige |
|---|---|
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| 1. september 2024 | 53 |
| 31. august 2024 | 54 |
| 30. august 2024 | 52 |
| 29. august 2024 | 50 |
| 28. august 2024 | 51 |
| 27. august 2024 | 49 |
| 26. august 2024 | 51 |
| 25. august 2024 | 56 |
| 24. august 2024 | 57 |
| 23. august 2024 | 60 |
| 22. august 2024 | 55 |
| 21. august 2024 | 55 |
| 20. august 2024 | 54 |
| 19. august 2024 | 52 |
| 18. august 2024 | 62 |
| 17. august 2024 | 62 |
| 16. august 2024 | 60 |