Equipment Responsible for Quality Control Laboratory

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Kalundborg

Would you like to help people with diabetes and other chronic diseases? Do you want to be part of shaping the innovative journey in Quality Control? Are you motivated by working with new equipment within the laboratory field and ensuring it is qualified for the intended use? If so, read more below and apply to become our new Equipment Responsible and Qualification employee! The position As Equipment Responsible within M1 Quality Control Laboratory, you will be working in a department handling a broad spectrum of tasks within laboratory equipment, qualification of equipment, automation, and implementation of new technology. The main task will be qualification and working in projects with new solutions, such as:
  • Laboratory equipment
  • Optimizing processes, and implementing changes
  • New robotic solutions
  • New automation projects in a laboratory setting
  • Challenge in existing processes in a respectful and constructive way
  • Ensure timely support and service of running equipment within department
  • As an equipment responsible you are expected to have a proactive approach to solving problems related to equipment used in the daily operations at the QC laboratory. You will be responsible for qualification of new equipment and already running laboratory equipment e.g., UPLC/HPLC, equipment for measuring Total Organic Carbon and other laboratory equipment such as balance, UV, Conductivity, Titration, pipettes etc., Furthermore you will work together with the users and the innovation team (QC4.0), on new equipment/robotic solutions so we together can reach a smarter and more automated future. We do this together – meaning that we need a team player with good communication skills. We will do our best to welcome you in the team and provide any necessary trainings for you to feel competent and an important part of our department. Qualifications Ideally, you have experience within laboratory equipment, or you have been responsible for similar equipment maintenance incl. troubleshooting, test and documentation. But we are open minded and are better looking for the right profile to suit the team. To succeed in this role, you preferably:
  • Hold a degree in natural sciences, engineering, pharmacology, laboratory or similar – alternatively have documented experience with equipment/projects as described above for the position
  • Have experience with equipment in the laboratory from the pharmaceutical industry or another GMP-regulated environment, as well as QC compliance experience.
  • Have experience with Lean and working with qualification and/or validation of chemical analysis from a laboratory in the pharmaceutical industry or in another GMP-regulated environment.

  • We do know that not all dreams come through, but we wish to see an experienced candidate with a great sense of curiosity, humour and structure, an open and positive mind and ability to work independently as well as in a team. About the department In Active Pharmaceutical Ingredients (API), located in Kalundborg, we produce insulin and GLP-1 to help people living with chronical diseases like diabetes and obesity. We always have many exciting projects across Novo Nordisk - some require entirely new setups to utilise the opportunities in contemporary technology, while other are more focused on optimising existing setups. The Manufacturing unit 1 in Kalundborg is the world’s largest insulin factory. We produce the active ingredients which are the main component in many of Novo Nordisk’s products including our new oral product Rybelsys® for which we have high expectations. API M1 is unique as we have the entire production chain gathered under one roof. About Novo Nordisk At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development to manufacturing, marketing, and sales – we’re all working to move the needle on patient care. Contact If you wish to learn more about the position, please call Berit Eskerod Olsen on +45 3075 1592. Deadline 17 December 2023. Please, note that applications will be reviewed continuously, and we hire when the right candidate is found, so do not hesitate, and apply as soon as you can. Please note that 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. We look forward to receiving your application in Danish or English. Please do not include a photo in your CV as it helps us to a fairer recruiting process with equal opportunities for all 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.


    Information og data

    Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".

    Arbejdsstedet er beliggende i Kalundborg.

    Jobbet er oprettet på vores service den 30.11.2023, 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.
    • Øvrige
    • Kalundborg

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