Senior Quality Assurance Professional

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Are you an experienced QA or Validation Professional with solid experience, who is eager to set direction and to ensure compliance, in close work with your stakeholders? Do you thrive in a constantly changing environment with various challenges and growth opportunities to handle? Do you believe in working together is better than working on your own? Our area is expanding, and we can offer a great working environment with high level of team spirit as well as highly skilled, ambitious, and engaged colleagues. We offer an exciting job opportunity that will match your experience and a desire for development. We are looking for a senior QA professional like you, with a high level of dedication and an innovative mindset, who thrives in a constantly changing and challenging environment. The position You will be a part of the qualification team in OFP, where you will be working with qualification/validation of the equipment, the utilities, and the facilities for oral drug product manufacturing. You will act as a QA for the facility, equipment and the quality management system to ensure that the qualification documentation for implementation and maintenance of equipment complies with internal and external requirements. You will also contribute to finding solutions for ad hoc questions and challenges within compliance of cGMP. You will influence and set directions in setting the right level of compliance, optimizing our processes by applying LEAN mindset and establishing new processes. Our continuing high level of audit and inspection readiness is always on top of your agenda. Meaning that you work with QA oversight, where you proactively together with your colleagues and stakeholders, identify areas where our compliance can be strengthened. Qualifications We seek a colleague who fits our team both professionally and personally. As a person you are open minded with a high level and energy, have an outgoing attitude and have strong communication and collaboration skills with both your colleagues in QA and stakeholders.
  • You hold a Master’s degree in chemical engineering, pharmacy or other relevant MSc.
  • You have a minimum of 7 years of experience within the pharmaceutical industry and/or validation/qualification experience.
  • You dare to challenge us in our way of working and have a desire to take initiative as well as responsibility for your own learning.
  • You are a role model for behaviour.
  • You are a dedicated team player who inspires trust and respect among colleagues and partners.
  • We operate both in a national and international environment, so you must speak and write Danish and English fluently
  • As an individual, you are open-minded, have a high-quality mind-set and works with high level of energy, an outgoing attitude and natural networking skills. About the department Oral Finished Products QA is a department with approximately 70 skilled and motivated colleagues. We work with assuring quality and compliance of the facilities, the equipment, QC lab, manufacturing development, as well the release of tablets for the market. We are proud to work in a fast-growing and ambitious part of Novo Nordisk. Working at Novo Nordisk
    At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth. Contact For further information, please contact Birgitte Riis-Klausen, Associate Manager at +45 30795450. Deadline Deadline to apply for the position is April 11th, 2023. Applications will be evaluated continuously, when received and candidates may be called for interview before the deadline. 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. 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 Måløv.

    Jobbet er oprettet på vores service den 10.3.2023, 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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