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    Quality and Training Coordinator - Måløv, Danmark - Novo Nordisk A/S - A1p

    Novo Nordisk A/S - A1p
    Novo Nordisk A/S - A1p Måløv, Danmark

    for 3 dage siden

    Novo Nordisk A/S - A1p background
    Fuldtid
    Beskrivelse

    Are you passionate about quality management and dedicated to fostering a culture of continuous improvement? Do you thrive on sharing your expertise and guiding colleagues through training and quality management? If so, you might be the perfect fit for the dual role of Quality and Training Coordinator in the Oral Analytical Development laboratories at Novo Nordisk in Måløv, Denmark.

    The Position

    As a Quality and Training Coordinator you will be responsible for supporting management and colleagues in maintaining our quality levels and in seeking new ways of working.

    Your main tasks in the job will be to:

  • Ensure a high-level GMP overview
  • Support daily operations with a focus on quality and training
  • Lead and coordinate quality and training issues as well as compliance activities across departments
  • Drive authority inspections and internal audits In this unique role, you will report to the department manager. You will play a pivotal role in both maintaining and elevating our training system and quality standards, collaborating with the QMS team across the CVP area. Qualifications To be successful in this role, you have:
  • A background in life sciences, pharmaceuticals, engineering or similar
  • Extensive experience in GMP
  • Knowledge about analytical laboratory processes
  • Experience building and maintaining training as well as QMS systems You have a quality mindset, coupled with the ability to work independently and serve as a role model setting the direction in Training, Quality and Compliance issues. About the Department You will be part of our Early- and Late phase analytical development laboratories for oral products, a subunit of CMC Development & Scaling, Drug Product & Analytical Development located in Novo Nordisk Park, Måløv, greater Copenhagen. The departments are responsible for both development and validation of analytical methods and QC release of oral products for preclinical and clinical trials. We are approx. 110 colleagues all together, working at non-GMP as well as GMP level. We offer a culture of collaboration and personal flexibility with a strong focus on continuous improvements. We especially have an interest in transforming our laboratories to become truly digital and automated.
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