Project Quality Management Controller

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Gentofte

Are you looking for a position where you can contribute to a structured way of creating quality documentation? Does the idea of being involved in a new capacity expansion project where you can influence and impact future active pharmaceutical ingredient (API) production sound interesting? Are you eager to work with complex problem-solving related to securing the common overall validation strategy? If yes, then you may read on to find out more about our new Project Quality Manager opportunity based in Hillerød. The position
As Project Quality Manager you are part of the project quality management work package for a new capacity expansion project. In this role, you have the responsibility to ensure follow-up on quality activities in the different monitoring tools setup from the work package. Furthermore, you will be part of the other activities related to the work package which is (but not limited to):
  • Standardisation of project specific templates
  • Ad hoc guidance for stakeholders in the project (internally and externally).
  • Collaboration with automation-, operational- and equipment responsible to ensure the common and agreed quality strategy as well as Quality Assurance (QA).
  • Writing project specific documents and supporting in the validation documentation.
  • Training in different quality standards used in the project
  • Responsible (in collaboration with the entire work package) for the project audits
  • This position is a great opportunity to contribute to implementing the direction for the quality structure and management in this new capacity expansion project. Qualifications To succeed in this role, we expect you to have:
  • A Master’s degree within biochemistry, chemical engineering, science, pharmacy or similar.
  • Experience within quality management system in the pharmaceutical industry is an advantage but not a requirement. Preferably, this also includes project activities.
  • Proficiency in spoken and written English. Fluency in spoken and written Danish is advantageous.
  • As a professional you are working independently, you thrive driving initiatives and have a forward-thinking outlook. As a person, you enjoy collaborating, learning and sharing information with others. You are driven by achieving great results together with colleagues. You possess excellent communication and collaboration skills enabling you to interact with your many stakeholders from different functions and parts of the organisation. About the department
    BRD API Denmark is in Gentofte, Hillerød and Kalundborg. This is where the active ingredients, going into all our life-saving biotech products, are made by app. 500 committed colleagues. We manufacture through complex chemical and biotechnological processes requiring a high level of expertise, commitment, and engagement from our employees and including cultivation, recovery, purification, and freeze-drying. We are producing at full speed in existing facilities, while building and ramping up new state of the art additions to keep up with demand and new Novo Nordisk products. We bring value to patients by delivering the purest possible high-quality API made in compliance with GMP. We drive change by always looking for improvements within our processes, but also in the way we work together to make our products reach as many patients as possible.
    Working at 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. 2500 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
    If you would like to discuss further, you are welcome to contact Project Manager Martin Rosenkjær at +45 34 48 32 48 Deadline
    10 April 2023. Applications are reviewed on an ongoing basis, so please submit your application as soon as possible. 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.


    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 27.3.2023, 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.
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