GMP supporter

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Gentofte

Does ensuring GMP compliance in our Warehouse Supply Chain and working with cutting-edge pharmaceutical production technology, sound like your next step? We can offer a position in a very exciting area in Novo, where we support several existing production lines. In the pipeline we have a couple of WH building projects, where we extend the facility. You will be a part of a team, that build up best practice processes for both existing and 3 new production lines with some of the newest pharma production technology. About the department The position is placed in the Warehouse Support and Procurement team, which is anchored in BRD Business Support in Biotech Rare Disease Finished Products Gentofte (BRD FP GEVA). The team consist of 15 people, where 8 people develop and supports production within our Warehouse division consisting of 3 Warehouse teams. We support the complex supply chain processes, that not only ensure timely deliveries but that our warehouses and logistic flow are complying according to all standards and requirements from the authorities. We also develop the way we work by implementing ideas for optimisation and capacity expansion of our processes, facilities, and warehouses using new technologies and innovative approaches. The work will also be carried out in close corporation with the management and employees in the warehouse teams right now counting 24 people and the many stakeholders, from whom we receive goods and products and to whom we send goods and products. The position
  • Your area of responsibility will revolve around support of maintaining GMP compliance, and will include:
  • Participation in inspections
  • Update and prepare instructions, procedures, and risk assessments ensuring they are up to date and ready to meet current GMP requirements.
  • Deviation handling, change request and reporting
  • Optimising processes within the area and across stakeholders
  • Participating in project
    • This job holds a range of professional opportunities to develop expertise in a complex manufacturing setup where ambitions are high. Qualifications You have experience in pharma production and regulation and have knowledge/or are keen in getting knowledge in the area of Supply Chain - an important area operating in the intersection of a broad number of production lines.
  • You have a Bachelor or Master education within relevant area ex. process/production technology, supply chain, chemistry, or pharmacy.
  • You have a degree within manufacturing or production engineering or warehouse logistic/supply chain and have experience working within the pharmaceutical or food industry under GMP regulation.
  • You are interested in new technologies and how to implement them to optimize our processes.
  • You have a pragmatic and it-can-be-done approach to your tasks, willingness to learn, and have experience in pharma production or a GMP regulated environment.
  • As a person you are systematic and have a structured way of working with your tasks. You have a positive attitude, a proactive behavior, and gain energy by working in close collaboration with your team colleagues and other stakeholders.
    • You enjoy knowledge sharing, and your quality mindset and solution focus is a natural part of you. You appreciate the value of accurate and timely documentation, as you know how important it is in relation to the safety and quality control. It is paramount for this position that you are fluent in Danish as well as in English, making it easy for you to facilitate and contribute to technical discussions. About Novo Nordisk In Novo Nordisk, it is your skills, dedication and ambitions that help us improve the lives of millions of people. With us, you will work with talented colleagues and be presented to lots of professional opportunities. Should you wish to learn more about working at Novo Nordisk, this may be an excellent place to begin: https://www.novonordisk.com/careers/working-at-novo-nordisk.html Contact If you have questions about the position, please call Mette Mørkeberg Brandt +45 30756737 from the 31. July to 6. August 2023. Deadline 09th August 2023. Applications will be screened on an ongoing basis, so you are encouraged to apply as soon as possible. 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 Gentofte.

    Jobbet er oprettet på vores service den 13.7.2023, men kan have været deaktiveret og genaktiveret igen.

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    Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
    • Øvrige
    • Gentofte
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