Validation Responsible

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Kalundborg

Would you like to be a part of a packaging and assembly factory of the future? Are you driven to use your knowledge and experience to help others succeed? Are you ready for a work life where focus is on quality and delivery of a life-saving medicines to our patients? Now you have the opportunity to be an active part and influence a vast number of colleagues in our department for Finished Production (FP) in IFP Kalundborg as our new Validation Responsible. The position Novo Nordisk is investing massively in new production lines in Kalundborg, where among other things we will pack products for patients who are suffering from obesity. This production is latest focus within Novo Nordisk treatments for our patients. With this expansion we will contribute with the important role of producing future products - and you will get an opportunity to be a part of it. We are seeking a validation supporter with experience within GMP regulated working environment, it is a benefit if you have experience from pharmaceutical industry, but it is not a prerequisite. You will be a part a support team in IFP Technical Support & Validation, consisting of 6 highly engaged and competent coworkers. We are known for our high professional level and ability to consistently deliver. Together with your colleagues you will lead and have the responsibility for:
  • Validation – using a Science and Risk-based Validation (SRV) approach
  • Preparation of validation documentation for both low and high complexity projects
  • Contribute to maintaining compliance across the department
  • Support with training and help the department within SRV concept
  • Preparation of validation plans
  • OPV/SE- Assist Supporters to maintain the validate state continuously
  • Qualifications For this position we are imagine that a successful candidate poses:
  • A relevant academic education - ideally an Engineer, Pharmacist, Chemist, or similar.
  • Several years of experience with validation in projects and preferably with validation/qualification within a GMP-environment.
  • A willingness to support a production, which at times can be characterized by a very dynamic working environment.
  • A good overview and a sharp analytical sense, which makes it easy for you to pin-point challenges and see connection between processes, materials, and equipment.
  • Previous experience within Finished production will be advantageous.
  • Proficiency in both oral and written English. Danish will be a great advantage too.
  • As a person you are responsible and able to execute necessary decisions to solve the challenges with flair for efficiency and quality. In this position you will have contact with many stakeholders and therefore we hope that you find it naturally to interact with other individuals and possesses a passion and motivation for the work you perform and is ready to take the lead. It is important that you thrive in a challenging, dynamic and changeable environment and no tasks is too big or too small to solve. We look forward to hearing from you, especially if you are proactive, constructive, solution oriented with flexible mindset. Even though you might not tick all the boxes, we would still like to hear from you and read your application - it may be that you are the one we are looking for! About the department You will be a part of Novo Nordisk finished production, which counts around 6.100 employees across seven production sites and five countries. We are the last, but very important part in value chain, before the finished products can be sent to patients all over the world. In Finished production in Kalundborg we are 270 employees, who are responsible to assembly and packaging of obesity and diabetic products on our fully automatic production lines. Working at 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, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care. Contact If you are eager to know more about the position, you are more than welcome to reach out to hiring manager Mathias Agergaard on phone +45 30 77 66 77. Deadline 31 May 2023. We will review applications and conduct interviews on an ongoing basis, so we encourage you to apply as soon as possible. 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. 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 Kalundborg.

    Jobbet er oprettet på vores service den 8.5.2023, 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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