Senior QA Profesional

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Deviation Area Process Manager Are you an experienced QMS or QA professional, 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? Then this is the area to apply for a job. The position 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 candidate like you, with a high level of dedication, an innovative mindset, who works independently and thrives in a constantly changing and challenging environment. The job is anchored in QA for Emerging Technologies and consists of 2 parts. You will be the Area Process Manager for the Deviation Process and coordinator for local audits in Emerging Technologies (ET). The Area Process Manager for the Deviation Process group has the responsibility for heading up the local ET process group and setting the direction for the deviation process, but also to be a Subject Matter Expert that can support both QA’s, stakeholders, and management. You will be ensuring the deviation process is in compliance with regulations, maintaining and performing training and participate actively in the corporate process group. As local audit coordinator you will be coordinating, supporting, and managing the audits in ET in DK in close cooperation with QMS coordinators and Line of Business managers. It entails organizing the audits and ensuring that everything is ready for the when the auditors arrive, which means you must coordinate getting the documentation for the auditors beforehand and running the audit back-office during the audit. Qualifications We seek a colleague who fits our team both professionally and personally.
  • You hold a master's degree in chemical engineering, pharmacy, or another relevant MSc
  • You have +6 years of experience in deviation/CAPA process from a GMP regulated environment.
  • We operate both in a national and international environment, so you must speak and write Danish and English fluently
  • You have experience with audits/inspections
    • Soft skills As an individual, you are open-minded, structured, have an outgoing attitude and have strong communication and collaboration skills with both your colleagues in QA, stakeholders, and managers. You are a role model for others and dare to make tough decisions, and inspire people, but also a team player who inspires trust and respect among colleagues and partners. About the department Emerging Technologies QA is an area with approximately 80 skilled and motivated colleagues. We work with assuring quality and compliance of the facilities, the equipment, QC lab, manufacturing development, as well as the release of tablets for the market. We are proud to work in a fast-growing and ambitious part of Novo Nordisk. Contact For further information, please contact Birgitte Riis-Klausen, Associate Manager at +45 30795450. Deadline Deadline to apply for the position is October 10th, 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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    Arbejdsstedet er beliggende i Måløv.

    Jobbet er oprettet på vores service den 12.9.2023, men kan have været deaktiveret og genaktiveret igen.

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