Senior Engineering Professional for Packaging Processes
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Værløse
Do you have experience with validation and ramp-up of a brand-new production line? Do you have excellent communication skills and a solid technical background? Would you like to work in a place where you can transform technical knowledge into robust and stable production?Then we might have the right position for you as our new Senior Engineering Professional for Packaging Processes. Apply today and become a part of our exciting expansion of the production capabilities in Kirke Værløse.The PositionAs a Senior Engineering Professional you will be hired into a newly established team who will support the validation, qualification and ramp-up of a new packaging line placed at our Kirke Værløse site in close cooperation with site Tietgenbyen in Odense.You are expected to have a solid understanding of the SRV concept for validation and qualification and the documentation aspects that shapes new production lines. Knowledge of the Fill Finish Expansion (FFEx) programme is an advantage.Your key responsibilities in this role will include:
• 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.
• Collaborating with key stakeholders such as technicians, supporters, operators, the project team in Odense, FFEx programme and Quality Assurance (QA).
• Contributing to ensure that all technical, quality and safety requirements are adhered to.
• Being part of implementing new regulatory compliance signals.To sum up – you live up to good engineering practice, can lift a new production into a stable production, and help ensure our sites’ licence 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 this role.QualificationsTo succeed in this role, you have:
• An academic degree within engineering, pharmaceutical science or similar field.
• 7+ years of experience working in a GMP environment and experience within the pharmaceutical industry.
• Experience with validation of packaging lines from a similar role.
• A strong LEAN mindset and experience with operational readiness and ramp-up.
• Strong competences within production equipment and utilities.
Furthermore, you are fully proficient in both written and spoken Danish and English language.
On a personal level, you have a positive mindset, and you are driven by achieving great results together with colleagues. You enjoy collaborating, learning, and sharing information with others. You have a structured way of working and enjoy take initiative and have a forward-thinking outlook. You can deep dive on details whilst keeping the broader picture at sight.Excellent communication and collaboration skills are essential in this role, making it easier to interact effectively with stakeholders both across and outside the organization.About the DepartmentFPM DK-2 is a part of Finished Product Manufacturing (FPM). At our sites in Gentofte and Kirke Værløse, we are more than 190 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 GMP in a timely and cost-effective way as we constantly optimise 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, but 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 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 recent technology.Contact
For further information, please contact Louise Baltser Rasmussen, Senior Manager, New Product Entry on or +.Deadline
21 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.
• 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.
• Collaborating with key stakeholders such as technicians, supporters, operators, the project team in Odense, FFEx programme and Quality Assurance (QA).
• Contributing to ensure that all technical, quality and safety requirements are adhered to.
• Being part of implementing new regulatory compliance signals.To sum up – you live up to good engineering practice, can lift a new production into a stable production, and help ensure our sites’ licence 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 this role.QualificationsTo succeed in this role, you have:
• An academic degree within engineering, pharmaceutical science or similar field.
• 7+ years of experience working in a GMP environment and experience within the pharmaceutical industry.
• Experience with validation of packaging lines from a similar role.
• A strong LEAN mindset and experience with operational readiness and ramp-up.
• Strong competences within production equipment and utilities.
Furthermore, you are fully proficient in both written and spoken Danish and English language.
On a personal level, you have a positive mindset, and you are driven by achieving great results together with colleagues. You enjoy collaborating, learning, and sharing information with others. You have a structured way of working and enjoy take initiative and have a forward-thinking outlook. You can deep dive on details whilst keeping the broader picture at sight.Excellent communication and collaboration skills are essential in this role, making it easier to interact effectively with stakeholders both across and outside the organization.About the DepartmentFPM DK-2 is a part of Finished Product Manufacturing (FPM). At our sites in Gentofte and Kirke Værløse, we are more than 190 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 GMP in a timely and cost-effective way as we constantly optimise 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, but 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 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 recent technology.Contact
For further information, please contact Louise Baltser Rasmussen, Senior Manager, New Product Entry on or +.Deadline
21 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 7.4.2025, 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.
- 07.04.2025
- Øvrige
- Værløse
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