Equipment design and qualification responsible

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Would you like to help us upgrade our pilot plant capacity within a growing portfolio of diabetes products? Do you want to expand your knowledge within pilot production, qualification and implementation of equipment used to purify insulins and GLP-1s of the future? If yes, then you could be our new colleague as Pilot Supporter. Apply today and join us for a life-changing career! The position We constantly focus on optimizations, and standardisation in our processes due to the expansion of our facilities and increasing production capacity. Your daily tasks and responsibilities will include:
  • implementation of new production equipment as well as changes to existing facilities for purification of proteins, where you will be responsible for commissioning and qualification
  • influence the design process as well as the department's technological development
  • solve both practical and documentation tasks, including preparation of change requests, qualification documents and instructions
    • In this position you will have the possibility to influence the development and get reliable insight into the workflows and procedures. We work with LEAN principles and offer you an opportunity to engage and take part in cross-organisational tasks and problem-solving. You will thereby influence the processes and contribute to the professionalism across a broad organisational area. As part of working in Novo Nordisk, you will also be exposed to various development opportunities during your daily work, catering to your interests, talents and the business needs of the future. Your Qualifications You have a technical education, such as an engineering degree or an education as a technician. A systematic approach and a strong quality-oriented mindset is expected. Furthermore, the following will be considered an advantage:
  • Experience within operating and maintaining plants and/or equipment
  • Knowledge of GMP or working in a pharmaceutical industry or other regulated industry
  • Knowledge of operating systems and interest in IT, as large parts of our equipment are controlled and monitored via DeltaV or Sattline
  • Experience with preparing documentation as change request, requirements specifications, equipment design, qualification, test protocols as well as deviations
  • Good process understanding
  • Flair for technical solutions and a pronounced professional curiosity
    • To succeed in this position, great collaboration and communication skills are key as you will work closely with different professional teams. A proactive, hands-on, and independent approach is needed. You are good in planning, work purposefully and take pride in driving and completing your tasks to the given deadlines. Finally, we also emphasize that you are a positive person, who can motivate others around you and is a visible team player. About the department We are 60+ employees in the Chemical Manufacturing & Control (CMC) API Pilot department, divided into five teams, three facilities, and two locations. Our task is to scale up processes and purify proteins for toxicological and clinical studies. We are part of the Novo Nordisk Product Supply, Quality & IT (PSQIT) unit, responsible for manufacturing and distributing products to markets and patients all over the world. You will be a part of a highly skilled team of academics and principal technicians, with the responsibility to ensure stable operation of production equipment and participate in the design, qualification, and commissioning of equipment. The team works closely with skilled project staff, scientists, process technicians and calibration technicians/craftsmen. 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 have any question, do not hesitate to reach out to hiring manager Christina Anne Storgaard at +45 3079 9502. Deadline July 15th, 2023. Applications will be reviewed continuously, and we will begin conducting interviews already during the posting period, so please do not hesitate to apply. 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.


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

    Arbejdsstedet er beliggende i Bagsværd.

    Jobbet er oprettet på vores service den 12.6.2023, men kan have været deaktiveret og genaktiveret igen.

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