GMP support for the facility and utility area, IFP Kalundborg

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Kalundborg

If your expertise covers the handling of Building Management System (BMS) and Facility Management System (FMS) activities in a GxP regulated production environment, this could be your chance to personally impact business-critical systems in the Life Science Industry. Bring your own personal ambition and dedication and join our team of highly qualified colleagues, with a passion to bring better treatments to the people who need them. You will be part of the "IFP KA Facilities management" team, where you will have skilled and ambitious colleagues, as well as a multitude of colleagues and contacts spread throughout the organization. It is the team's responsibility to ensure that we comply with regulatory requirements for the operation and maintenance of the building and building-related processes as well as our utility facilities. It is very crucial that we maintain compliance and stable operations so our products can be packed at our highly efficient factory. The team's areas of responsibility are wide-ranging and covers e.g. the building facility with associated equipment and utility facilities incl. controlling and monitoring IT systems such as BMS & FMS, but also building-related processes such as cleaning, pest control, calibration, access control and waste destruction. The position As our new GMP Supporter you will work closely with your colleagues at the Facilities Management team and the Facilities Engineering team. We provide GMP support related to our building operations and utility systems, including ventilation and cooling systems. This means ensuring that all relevant requirements are reflected in local procedures, handling change control, preparation of risk assessments, deviation processing, systematic problem solving, trend reporting, validation activities etc. You will be responsible for your own area related to room conditions for temperature and humidity. You will be working with different kind of IT systems primary BMS system and FMS system and secondary Testo Savaris project related monitoring system. Therefor it is important you have flair and interest within IT. Your key responsibilities will be:
  • You will have to present relevant cases for audits and inspections, usually in English.
  • You must oversee the planning and implementation of i.e.. smaller optimization projects in own area
  • You support the team's technicians with your GMP knowledge and experience
  • You have experience working with cLean standards for i.e board meetings and ongoing.
    • Qualifications
  • You have a relevant academic education, within engineering or pharmacy or similar - but a background as a technician/craftsman could also be relevant.
  • You are fluent in spoken and written English and Danish or you have a willingness to learn Danish
  • You have a good understanding of i.e. HVAC and control/monitoring systems such as BMS/FMS
  • You have experience from support and/or project work in a GMP regulated company. Experience working with validation will be an advantage
  • Experience of working according to cLean standards is also an advantage
  • You have a systematic, proactive approach, are precise and have a good overview
    • As a person, you have a proactive approach to work, it is natural for you to take responsibility and you can make decisions independently. You are motivated by contributing to change and driving processes in an environment with many stakeholders. About the department and the team You will be part of Novo Nordisk injectable finished product production, which has more than 6,000 employees across 7 production sites and 5 countries. We are the last but important link in the value chain before the finished products can be sent to patients all over the world. We invest in expanding capacity and have an important role in the manufacture of the products of the future. In IFP Kalundborg, we have 280 employees who are responsible for assembling and packaging Novo Nordisk products on our fully automatic production lines. Contact For more information, you can contact hiring manager Camilla Emilie Favrholdt +45 30 75 63 38. Application deadline May 29, 2023 - we process applications and hold interviews on an ongoing basis, so please send yours as soon as possible. We would like to ask you not to include a photo in your CV, as it helps us to have a better and fairer process.In your application, you are welcome to make it clear whether you only want to be considered for permanent positions, or whether you are also applying for temporary ones. 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 24.3.2023, men kan have været deaktiveret og genaktiveret igen.

    Rapportér
    Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
    • Øvrige
    • Kalundborg
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