QC Professional

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Are you passionate about analytical chemistry? Do you want to play a pivotal role in setting up a new laboratory and ensuring high-quality standards? Are you able to take ownership, act and complete tasks full circle, thus secure there are no loose ends? If yes, read more and apply today for a life-changing career. The position As our new QC Professional, your key responsibilities will be:
  • Prepare project plans and coordinate with stakeholders across the organisation to support that the new laboratory will be up and running within the deadline.
  • Qualify, validate, and implement respective analytical equipment and analytical procedures.
  • Collaborate with your colleagues to deliver quality control of high standards.
  • Continuously improve and optimise our processes.
  • Provide sparring and problem-solving with laboratory technicians on analytical results.
  • Review analytical reports and handle tasks within our Quality Management System (QMS) to ensure compliance with external and internal requirements.
    • As we work under GMP requirements, Change Requests, SOP updates, deviations, etc., are a natural part of the job. Qualifications To succeed in this role, ideally you will have:
  • A scientific academic degree such as cand. pharm., cand. scient., chemical engineer or similar.
  • Experience with validation of analytical procedures and qualification of analytical equipment.
  • Experience in the use of data analyses and statistics, complimented by good IT skills.
  • Strong quality mindset and always strives for excellence.
  • Strong communication skills and proficiency in both written and spoken Danish and English.
    • Knowledge in our analytical techniques is an advantage e.g Äkta and GC. On a personal level, you are a team player who is solution-orientated and have a positive attitude. You have good communication skills and can establish and nurture relationships across teams and departments. We are digitally transforming our QC laboratories, introducing automated processes and connectivity to support a paperless future. You are expected to contribute to this journey by being curious about new and innovative solutions and ensuring their successful implementation. Embracing change and proactively bringing forward new solutions, processes, and improvements are key qualities we are looking for in the ideal candidate. Moreover, you are comfortable in a dynamic environment where priorities shift rapidly. About the department We are about 35 employees in the Quality Control unit organized in three teams, consisting of Specialist, Professionals and Laboratory Technicians. You will be joining the QC Resins team where we are 7 employees. We have many different analytical techniques such as GC, ÄKTA, BET, Elemental Analysis, Karl Fisher etc. The QC Resin team will move to a new location next to Køge Nord st. when the laboratory is up running in 2026. You will contribute to this transfer by preparing project plans and qualification documents for new/relocation of equipment, validation documents for transferring analytical procedures, etc. The team support development of products and production with high quality analyses. The team also handle tasks like stability tests, raw material controls, implementation of new analytical equipment, development, and validation of methods, etc. Working at Novo Nordisk Novo Nordisk Pharmatech A/S (NNPR) is located in Køge, Denmark, and is 100% owned by Novo Nordisk. The company has close to 450 employees and the core task of the business is to enable better medicines through biopharmaceutical manufacturing for Novo Nordisk as well as for the global industry. NNPR is in the coming years expanding an already wide product portfolio within Enzymes, Synthetic Molecules, and Resins. The company has the full value chain with both R&D laboratories, production facilities, and a commercial organisation, plus a wide range of support departments on top. Contact For further information, you can contact Manager, Louise Frische, on +45 30370023. Deadline
    1 September 2024 You may submit your application in English or in Danish. We will take candidates into the recruitment process continuously, so do not hesitate to apply today. 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 Køge.

    Jobbet er oprettet på vores service den 13.8.2024, 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.
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