Øvrige i Hillerød

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Hillerød

We are looking for a skilled GMP supporter who would like to be part of a highly skilled production unit dedicated to making a difference for people living with Haemophilia and other chronic diseases.

About the production department

You will be part of a dynamic business area which produce Active Pharmaceutical Ingredients (API) for patients across the world.

BRD API DK production site 25K 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 Job

You will be a part of a group of employees responsible for raw material handling and warehouse for API production. This includes raw materials for market products as well as implementing raw materials for new products in phase 3 clinical production. The term “raw materials” includes both eg. chemicals, media and single use equipment such as bags, filters, special made tubing sets etc.

As a supporter for raw material handling your responsibility is to ensure the implementation and logistics of new and current raw materials for production. You will in close collaboration with process supporters, SAP supporters, Raw Material Supply Management and warehouse (internal in production and NN warehouse) ensure the timely identification and implementation of new raw materials for phase 3 and market production. Being part of production, you are a key stakeholder and responsible for contact to our sourcing and logistic departments in Novo Nordisk. A strong GMP mindset and focus on stakeholder management is central in this position.

Your key tasks will be:

  • Communication with sourcing and logistic departments
  • Coordination of activities in production associated with raw materials
  • Ensure timely identification and implementation of (new) raw materials for phase 3 and market production
  • Responsible for forecast of raw materials for production
  • Responsible for needed change requests and deviation handling
  • Following up on day-to-day tasks in the production e.g. issues and questions on raw materials or the documentation in e.g. log books

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 in raw material handling and SAP.

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 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
The 6th of November 2022. We may conduct interviews before the deadline. Therefore, we may take the liberty to close for new applicants before the deadline

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 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 13.10.2022, 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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