Process Supporter
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Værløse
Do you have experience with supporting packaging lines in a pharmaceutical setting? Do you have excellent communication skills and a solid background in operational processes? Do you enjoy working in a technical area where quality and compliance is mandatory and would you like to work in a place where you can shape processes into robust and stable production?
If yes, then join us as our new Process Supporter. Apply today and become a part of our exciting expansion of the production capabilities in Kirke Værløse.The Position
As a Process Supporter at , you will be hired into a newly established team who will support the validation, performance verification (PQ) and ramp-up of a new packaging line placed at our Kirke Værløse site in close cooperation with site Tietgenbyen in Odense.
You will be working in close collaboration with different stakeholders both internally and with other production sites to ensure high quality, efficiency, reliability, and stability for the production. Your key stakeholders will be technicians, supporters, operators, the project team in Odense, Fill Finish Expansion (FFEx) Programme and Quality Assurance (QA).
You will contribute to ensure that all compliance, quality and safety requirements are adhered to, and you will be part of implementing new processes based on compliance signals.
The key tasks will include:
• Deviation handling during our ramp-up phase.
• Perform systematic problem solving on process and equipment issues.
• Work with daily improvement of the new packaging line.
• Ensure compliance with current rules and regulations.To sum up – you live up to good manufacturing practice, can lift a new production into a stable production, and help ensure our sites’ license to operate.
You should expect to be working from our production site in Kirke Værløse, however, some travel to our site in Odense is expected and vendor visits may be part of the job.
Qualifications
You will be a great asset to our team because you have:
• An academic degree within natural science or engineering (e.g MSc in Pharmacy, Science, Engineering or equivalent).
• Preferably +2 years of experience within a similar role in a GMP regulated environment.
• A strong cLEAN mindset with experience in systematic problem-solving.
• Experience with handling and preparing deviations and editing QMS documents.
• Great communication skills with the ability to build relations with stakeholders.
• Full proficiency in oral and written English and Danish.As a person, you take initiative naturally and have a strong personal drive and dedication. Bringing a good sense of humor to work even when pressure is on and thrive in a changing and dynamic environment is also important. You demonstrate attention to detail, and you are structured in your problem-solving approach. Furthermore, you need to embrace professional and personal diversity.
About the Department
FPM DK-2 is a part of Finished Product Manufacturing (FPM). At our sites in Gentofte, Kalundborg, Kirke Værløse and Taastrup, we are more than 350 colleagues working together to ensure that our finished products are assembled and packed to the highest standards before distributed to people living with serious chronic diseases. We bring value to our patients by delivering high-quality products in accordance with Good Manufacturing Practice (GMP) in a timely and cost-effective way as we constantly optimize our processes and invest in the latest technology.
Working at FPM,
Finished Product Manufacturing (FPM) is a part of 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 6,000 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.Contact
For further information please contact Senior Manager, Louise Baltser Rasmussen at +.
Deadline
27 April 2025.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.
If yes, then join us as our new Process Supporter. Apply today and become a part of our exciting expansion of the production capabilities in Kirke Værløse.The Position
As a Process Supporter at , you will be hired into a newly established team who will support the validation, performance verification (PQ) and ramp-up of a new packaging line placed at our Kirke Værløse site in close cooperation with site Tietgenbyen in Odense.
You will be working in close collaboration with different stakeholders both internally and with other production sites to ensure high quality, efficiency, reliability, and stability for the production. Your key stakeholders will be technicians, supporters, operators, the project team in Odense, Fill Finish Expansion (FFEx) Programme and Quality Assurance (QA).
You will contribute to ensure that all compliance, quality and safety requirements are adhered to, and you will be part of implementing new processes based on compliance signals.
The key tasks will include:
• Deviation handling during our ramp-up phase.
• Perform systematic problem solving on process and equipment issues.
• Work with daily improvement of the new packaging line.
• Ensure compliance with current rules and regulations.To sum up – you live up to good manufacturing practice, can lift a new production into a stable production, and help ensure our sites’ license to operate.
You should expect to be working from our production site in Kirke Værløse, however, some travel to our site in Odense is expected and vendor visits may be part of the job.
Qualifications
You will be a great asset to our team because you have:
• An academic degree within natural science or engineering (e.g MSc in Pharmacy, Science, Engineering or equivalent).
• Preferably +2 years of experience within a similar role in a GMP regulated environment.
• A strong cLEAN mindset with experience in systematic problem-solving.
• Experience with handling and preparing deviations and editing QMS documents.
• Great communication skills with the ability to build relations with stakeholders.
• Full proficiency in oral and written English and Danish.As a person, you take initiative naturally and have a strong personal drive and dedication. Bringing a good sense of humor to work even when pressure is on and thrive in a changing and dynamic environment is also important. You demonstrate attention to detail, and you are structured in your problem-solving approach. Furthermore, you need to embrace professional and personal diversity.
About the Department
FPM DK-2 is a part of Finished Product Manufacturing (FPM). At our sites in Gentofte, Kalundborg, Kirke Værløse and Taastrup, we are more than 350 colleagues working together to ensure that our finished products are assembled and packed to the highest standards before distributed to people living with serious chronic diseases. We bring value to our patients by delivering high-quality products in accordance with Good Manufacturing Practice (GMP) in a timely and cost-effective way as we constantly optimize our processes and invest in the latest technology.
Working at FPM,
Finished Product Manufacturing (FPM) is a part of 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 6,000 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.Contact
For further information please contact Senior Manager, Louise Baltser Rasmussen at +.
Deadline
27 April 2025.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 Værløse.
Jobbet er oprettet på vores service den 10.4.2025, 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.
- 10.04.2025
- Øvrige
- Værløse
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