GMP Supporter, API Production

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Hillerød

Would you like to be part of a highly skilled production unit dedicated to making a difference for people living with Haemophilia and other chronic diseases. Then keep on reading.

About the production department

BRD API DK production consists of 3 departments covering 11 teams. We are situated in Hillerød and produce products for chronic diseases as for example haemophilia disorders. As we implement several new products in the upcoming years, we are responsible for both market production, phase 3 GMP productions as well as process validation.

The open position is in New Product Entry & IT, which is linked to the production department.

The Job

You will be part of the production area and your tasks will be:

  • everyday support to stakeholders
  • super user representative ARSU-WH and ARSU-PROD
  • coordination of central activities related to SAP/Syncade
  • training in basic functions and maintaining the compliance side of the systems
  • supporting in creating MAF, AMAF and BOM for production
  • handling Idoc’s
  • implementing of new products in SAP production and new raw materials in SAP warehouse

We work cross functionally in project teams, and together we succeed in finding solutions. As a GMP Supporter you work in close collaboration with our process supporters and will be one point of entry to finance and logistic. As our facility has a Manufactuirng Execution System (MES) you need to be able to understand the interface with SAP and work closely together with colleagues from IT/OT as well.

Qualifications

You have an education as bioengineer, biotechnologist, process technician, laboratory technician or similar and have at least 5-8 years of experience with production of pharmaceutical products under GMP. Preferably you have experience with SAP for the use in warehouse and/or production. An understanding of Syncade and/or PAS-X is an advantage.

As a person, you are able to work independently and are used to work on multiple tasks in a complex daily business. You are structured and proactive with very good planning skills and have an overview over your tasks. Excellent written and spoken communication skills in both Danish and English are a must, as you will have several stakeholders across the organization. In your work you will never compromise on quality. GMP and LEAN is a natural part of your skill set. To succeed you need to be able to keep calm and make decisions in a busy work environment where the agenda changes frequently.

Contact

For further information please contact Christiane Wiendahl at +45 30 79 48 62.

Deadline

14th December

Please note that interviews will be carried out on an ongoing basis, so you are encouraged to apply as soon as possible, 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.

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Information og data

Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".

Arbejdsstedet er beliggende i Hillerød.

Jobbet er oprettet på vores service den 5.10.2022, 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
  • Hillerød

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