Experienced and independent QA Supporter

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Måløv

Are you an experienced QA supporter with effective communication skills who is eager to set direction and to ensure compliance, in close collaboration with colleagues and stakeholders? If so, we have a position in a fast-growing tablet production in Måløv. You will be part of a team with responsibility for quality assurance for Quality Control laboratories in Oral Finished Product QA. We can offer a great working environment with prominent level of team spirit as well as highly skilled, ambitious, and engaged colleagues. In OFP (Oral Finished Products) QA our department consists of colleagues based in both Måløv and Durham US. The job In QA we have quality oversight and are physically present in the QC laboratory to observe performed processes and help solve issues in real time. You will review and approve laboratory related documentation including deviations, change requests, SOPs (Standard Operating Procedures) etc. You have a risk-based approach to the laboratory, and you contribute to find the right balance between patient safety, compliance to requirements and effective business conduct. We can offer an exciting and challenging position, where you become part of a competent team with mainly QA Professionals who act as sparring partners and problem solvers in quality issues for the production. Qualifications
  • Ideally, you have a background as pharmacologist, laboratory technician or corresponding qualifications and experience within the pharmaceutical industry.
  • You have 5+ years of experience with GMP, quality assurance, QC laboratory or production support.
  • It is an advantage if you speak and write Danish.
  • You are an open-minded person with elevated level of energy, an outgoing attitude and have effective communication and collaboration skills.
  • You are a self-driven and independent person with a high sense of responsibility and initiative who can prioritise your many different tasks.
  • You thrive in a dynamic environment, where teamwork is on the top of the agenda, and like working with many different stakeholders.
    • About the department Oral Finished Products QA is a department which employs approximately 60 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. Contact For further information, please contact Associate Manager Christina Halberg +45 3075 9031. Deadline 7. March 2023. Application in Danish is also acceptable. Please note that applications will be reviewed continuously, and interviews will be planned as soon as a suitable candidate is identified. 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 Måløv.

    Jobbet er oprettet på vores service den 14.2.2023, men kan have været deaktiveret og genaktiveret igen.

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    Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
    • Øvrige
    • Måløv
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