GMP Supporter
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Kalundborg
Do you want to be part of an organisation that makes a difference for thousands of people every day? Can you maintain an overview and ensure compliance in a dynamic environment? Are you good at problem solving and are a team player? Do you enjoy being able to use your analytical approach to optimise and improve processes? If so, read more and apply today for a life-changing career as a GMP supporter at the warehouse within Finished Products Manufacturing (FPM) based in Kalundborg!
The position
As our new GMP Supporter, you will be welcomed into a team of 12, and will be involved in various daily tasks to support the warehouse and logistics departments with GMP Support. If you are looking for a varied role where you can apply your strong GMP experience to develop strategy, provide solutions and implement new processes through working closely with other departments, then this role could be for you! In addition to documenting quality incidents within the warehouse and providing guidance to operators about the correct procedures for documenting events accurately, you will also be responsible for: Handling quality issues in the warehouse Investigating and reporting deviations Supporting Warehouse and Logistics, in the processes Participate in workshops, tests or fix issues with proposed improvements in our processes Updating and improving SOPs Training of operators in new tasks Systematic problem-solving Present cases at internal audits and authority inspections No two days are the same, the interface is very wide and there are often new issues to follow up. We are excited the warehouse is about to be automated! Therefore, our new colleague is willing to alter existing processes, utilise LEAN principles to optimise them and actively seeks to improve the entire department alongside the team. Qualifications
Your experiences include: Degree or equivalent in Pharmacy, Chemistry, Engineering or related field. The ideal candidate has 2-4 years of work experience within GMP in the pharmaceutical industry. Experience working in other highly regulated industries is also of interest. Hands-on approach to executing processes and solving challenges amongst stakeholders within the department and cross functionally. Fluency in spoken and written Danish and English. You see yourself as a fast learner with strong analytical skills to gain oversight of complex processes and issues. You thrive taking on challenges and able to take the lead, show initiative and prioritise to work systematically to resolve them within deadlines. Since you will be working closely in the team and cross functionally, great communication skills are important to support driving the strategy. About the department
Finished Product Manufacturing (FPM) is a part of Novo Nordisk Product Supply, a global production network at the forefront of technology and quality production of pharmaceutical products. At FPM, we not only manufacture all finished products for people living with serious chronic diseases, we also use our competencies to drive technology leadership and improve standards across our core technologies to support the growing efforts into completely new production platforms and therapy areas for . Our global network consists of around 4,000 colleagues across ten countries. Here, we are responsible for the manufacturing of all finished products, including devices, needles, assembly, and packaging. As more and more people need our products, we support 's initiatives in new therapy areas. Every day, we strive to streamline and expand our capacity through process innovation, automation, and the introduction of new technology. Working at
At , we don’t wait for a 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 want to know more about the position, please contact Lars Mengel (Manager) at: +. Deadline
8 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 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 new GMP Supporter, you will be welcomed into a team of 12, and will be involved in various daily tasks to support the warehouse and logistics departments with GMP Support. If you are looking for a varied role where you can apply your strong GMP experience to develop strategy, provide solutions and implement new processes through working closely with other departments, then this role could be for you! In addition to documenting quality incidents within the warehouse and providing guidance to operators about the correct procedures for documenting events accurately, you will also be responsible for:
Your experiences include:
Finished Product Manufacturing (FPM) is a part of Novo Nordisk Product Supply, a global production network at the forefront of technology and quality production of pharmaceutical products. At FPM, we not only manufacture all finished products for people living with serious chronic diseases, we also use our competencies to drive technology leadership and improve standards across our core technologies to support the growing efforts into completely new production platforms and therapy areas for . Our global network consists of around 4,000 colleagues across ten countries. Here, we are responsible for the manufacturing of all finished products, including devices, needles, assembly, and packaging. As more and more people need our products, we support 's initiatives in new therapy areas. Every day, we strive to streamline and expand our capacity through process innovation, automation, and the introduction of new technology. Working at
At , we don’t wait for a 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 want to know more about the position, please contact Lars Mengel (Manager) at: +. Deadline
8 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 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 19.8.2024, 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.
- 19.08.2024
- Øvrige
- Kalundborg
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Statistik over udbudte øvrige i Kalundborg over tid
| Dato | Alle jobs som øvrige |
|---|---|
| 15. september 2024 | 50 |
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| 13. september 2024 | 53 |
| 12. september 2024 | 48 |
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| 10. september 2024 | 45 |
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| 1. september 2024 | 53 |
| 31. august 2024 | 54 |
| 30. august 2024 | 52 |
| 29. august 2024 | 50 |
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| 27. august 2024 | 49 |
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| 25. august 2024 | 56 |
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| 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 |