Maintenance Supporter

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Kalundborg

Are your analytical skills strong and do you enjoy a hands-on approach to your field? Can you add to the success story of Novo Nordisk and ensure the highest level of quality in the production of life-changing medicine to biopharmaceutical products worldwide? And would you like a range of opportunities for personal and professional development? Then you might be the next member of our dedicated support team. About the department In BioPharma, we produce a range of products that help people live with chronical diseases like hemophilia and hormonal imbalances. In our new filling and inspection facility, we will be filling the Active Pharmaceutical Ingredients (API) onto vials and dosage systems. In other words, we make the products ready for packing and distribution with all the processes that are involved in this – from various visual inspections over actual filling procedures to all the documentation that is necessary for us to comply with regulatory and quality standards. Our filling and inspection facility is ready to enter the next phase, and now we are looking into a period of production ramp up, which in turn initiates many processes optimization projects. You will be part of a support team of dedicated and talented academics and technicians. Our tone is relaxed, and if you enjoy sharing your knowledge and learning from others, you will enjoy working here. The facility is located at our site in Kalundborg with approximately 350 employees. The position As process supporter, your primary goal is to ensure that the production consistently delivers a high-quality product in compliance with internal quality requirements and GMP. Our team supports the production on shop floor, and our field of responsibility for the filling processes covers the validation of the lines, the operational procedures to operate them, the expertise in the products and the continuous improvement of the filling lines. This means that whenever something is out of the ordinary, we are the ones who help make everything run again as quickly as possible. When something needs changing, we ensure that the right validation procedures are in place, challenging external vendors on specifications and technical issues when necessary. The main role in this position is Guarantee the Validation Status in our Equipment and Process, Equipment qualification and be responsible for managing/participating in SPS related to DV´s in own team. Your main tasks will be, to support the following:
  • Development of competences,
  • Work in compliance with some SOP,
  • Build maintenance strategy, plans and frequency, Maintenance Work Description [MWD],
  • Change Control for related equipment
  • Ensure machine safety [CE marking].
  • You will Support the future maintenance strategy and operational platform [LCM], support end user training setup for operators and maintenance teams, to ensure faster support for production units, optimization of equipment according to future strategy You will be handling a range of stakeholders with diverse and possibly conflicting needs and concerns in a way that ensures the optimal collaboration across professional and cultural distances – and has the continuation of a stabile production chain as a result. You will be taking part in systematic problem-solving processes, development- and optimization projects and develop a broad understanding of a complex value chain, when you provide our collective expertise across a truly global organization. Furthermore, when you are ready, you will support the development of competencies in our production team and participate in audits and inspections. Qualifications
  • You hold a degree in biochemistry, bioengineering, automation engineering, or similar.
  • Preferably, you have 2+ years of experience from the pharmaceutical industry after graduating and have knowledge about aseptic production and behavior as well as current knowledge in process automation in biotech.
  • You are fluent in English, Danish will be a plus
  • You have great interest in working with GMP and LEAN.
  • You have good communication skills and the ability to efficiently work with concurrent tasks
  • As a person, you are open and honest, independent as well as team player and flexible to changes. Being proactive, responsible and energetic is a key to succeed in this position. In return, you will find opportunities for personal and professional development here that will be hard to come by elsewhere. Working at Novo Nordisk At Novo Nordisk, we have been changing diabetes since 1923. If you are ready to help us strengthen our position as an innovative pioneer and respected industry leader, we encourage you to join us and make the most of your talent. Contact Should you wish to learn more about what it is like working in Novo Nordisk, here is a good place to begin: https://www.novonordisk.com/careers/working-at-novo-nordisk.html
    For further information about the position, please feel free to call Julio Santiago, 34 48 06 96.
    Deadline 31 August 2023. 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 3.8.2023, 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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