GMP Coordinator

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Hillerød

Are you passionate about having a central role in a dynamic department with tasks that involve close collaboration with many stakeholders on a daily basis? Do you have a solid understanding of Quality and of Good Manufacturing Practice-regulated laboratory environments? If yes, you might be exactly the one we are looking for to join our team. Apply today! The Position As our new GMP coordinator, you will be the department's quality manager and become part of the department's management team. Together with other Good Manufacturing Practice (GMP) coordinators in Biotech & Rare disease QC (BRD QC) Hilleroed, you will have the opportunity to work with many exciting tasks across the area. You will be a daily sparring partner regarding quality issues, carry out ongoing GMP training and run quality-related projects in the department and in collaboration with the other GMP coordinators in BRD QC. You will:
  • Drive preparation for and follow-up on authority inspections and internal audits
  • Ensure high-level GMP overview and report quality trends to management
  • Lead and coordinate critical quality issues and compliance activities in the department and across if necessary.
  • Work in the Quality Management System – Delivery to Quality Management Review (QMR).
  • Support daily operations with quality and ensure a high level of GMP in the department.
  • Support and run DVs if necessary.
  • Run smaller projects in the department.
    • Qualifications To be considered for this position you have:
  • An academic degree (BSc or MSc) in natural science, engineering or similar.
  • Preferably + 3 years of experience from pharmaceutical industry.
  • You are familiar with complex quality processes and have experience from GMP-regulated areas.
  • Experience with LEAN is an advantage, as it is an integral part of our everyday life.
  • Proficiency in both English and Danish is a requirement.
    • You are someone who can interact and communicate at all levels in the organization, and you have an outgoing and relaxed personality. You take pride in solving your tasks and challenges as close to the process as possible, with close involvement of your key stakeholders. It is important that you can think and act with a broad and holistic perspective and see the big picture without losing sight of or interest in important details. We are looking for a GMP coordinator who does not compromise on quality and has the drive to set the direction for the department's quality level. About the Department Our team is part of the BRD Quality Control area that is based in Gentofte, Hilleroed and Kalundborg. Here we are app. 270 colleagues who support the biotech production with a selection of chemical and microbiological analysis of product samples, crucial for always making sure the product is in high quality and ready for release to patients. We bring value to patients by delivering timely and reliable results that keeps production in control. We drive change by always looking for improvements and innovation within our processes - testing and implementing 4.0 technology to make the process even smoother and faster for the benefit of the patients. Working at BRD, Novo Nordisk Biotech & Rare Disease (BRD) is part of Novo Nordisk Product Supply, which is a global production network at the forefront of technology and in quality production of pharmaceutical products. In BRD we are not only supplying all Novo Nordisk products for Rare Diseases, but also using our competences in Biotech to support the growing efforts into completely new production platforms and therapy areas for Novo Nordisk. We are app. 2650 colleagues committed to drive change for people with serious chronic diseases. We produce our life-saving medicines out of five state-of-the-art production sites in Denmark and United States - covering the entire production value chain where raw materials are cultivated, purified, formulated, filled, assembled in devices, packed, and distributed across the globe. Not only are we making a difference for patients – we are also stiving to make a difference for our employees by promoting a learning culture with high level of trust, innovation, and development for everyone. Are you ready for a life-changing career? Contact For further information, you are welcome to contact Line Rossen at +45 3075 2313. Deadline 21 July 2023, but applicants are reviewed on an ongoing basis. 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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    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 14.4.2023, men kan have været deaktiveret og genaktiveret igen.

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