Inspection Specialist

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Do you want to be a part of the development of the future Aseptic Processing (AP) facilities future in a large global pharmaceutical company? Are you considered an expert within the Automated Visual Inspection processes of cartridges, pre-filled syringes, or vials? Then you might be the Inspection Specialist we are looking for to develop and support implementation of the technology solutions needed to drive the establishment of our new Aseptic Processing modules across the world. Apply now for this exciting job opportunity! The position We are looking for an experienced Inspection Specialist to support the significant expansion of the Aseptic Processing capacity across the Novo Nordisk manufacturing network, with the purpose of improving the lives of people. As Inspection Specialist, you will be a key player in specifying the automated visual inspection solution, together with our central manufacturing development team, the senior project manager, other specialists, and subject matter experts within the inspection process track in the AP Expansions programme. The inspection work package is responsible for delivering a multiformat fully automated visual inspection solution, designed for an in-line connection with the filling line. The work package also includes the design of the buffering solution between the filler and inspection unit as well as the handling of different incoming and outgoing package formats. The ambition is a system with a very low level of false rejects, high reliability and with the built ability to drive process optimizations through deep learning as an example. The key tasks will be:
  • Development of new technical standard for an in-line high speed tubs-based multi format automated visual inspection line
  • Setting the direction to ensure a risk-based approach to validation and maintaining the validated state of the equipment (including calibration and maintenance strategy approach)
  • Providing guidance in the creation and review of design documentation as well as design and definition of CQV (Commissioning, Qualification and Validation) activities within your area of responsibilities (FAT, SAT, IQ/OQ) to ensure a quick ramp up
  • Key player in design reviews and vendor oversight during the equipment design, build and test phases
  • Design and implement training setup for operations with focus on a high reliability operation and minimal operator interaction
  • Qualifications
    To be successful in this role you need to have:
  • An academical degree within engineering, natural sciences, or similar education
  • +10 years of work experience within automated visual inspection, with significant experience in small volume injectables
  • Significant experience from the pharma industry or other regulated industry where GMP (Good Manufacturing Practices) or similar requirements exist
  • Significant experience from project work including introduction of new technologies or processes
  • A quality mindset and a drive to create the “right” solutions while challenging the status quo
  • An excellent command of verbal and written English; command of Danish, French or Chinese in addition is a plus as some traveling to China, France, USA and within Denmark might be required
  • As a person, you take initiative naturally and have a strong personal drive and dedication. You need to bring a good sense of humour to work even when pressure is on, and you thrive in a changing and dynamic environment. You demonstrate attention to detail, and you are structured in your problem-solving approach. Furthermore, you embrace professional and personal diversity. About the department
    Technology Standards is a department in the newly created SVP area of AP Expansions which is anchored within Product Supply, which globally accounts for +19,000 of Novo Nordisk’s +44,000 employees. The responsibility of AP Expansion is to plan and execute the establishment of new aseptic filling capacity across the global manufacturing network within BioTech and Rare Diseases (BRD) and Injectable Finished Products (IFP) for new filling platforms while ensuring harmonisation and global standards. Across the different roles there is a distinct global aspect as the end goal is a global standard and best practice, and working with multiple sites, cultures and traditions will be a key element. Working at Novo Nordisk
    We are a proud life-science company, and life is our reason to exist. We’re inspired by life in all its forms and shapes, ups and downs, opportunities, and challenges. For employees at Novo Nordisk, life means many things – from the building blocks of life that form the basis of ground-breaking scientific research, to our rich personal lives that motivate and energise us to perform our best at work. Ultimately, life is why we’re all here – to ensure that people can lead a life independent of chronic disease.

    Contact
    For further information please contact Senior Project Manager, José Andres Salom Garcia at [email protected] Deadline
    19 February 2023 We will review applications and conduct interviews on an ongoing basis. 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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    Jobbet er oprettet på vores service den 14.10.2022, men kan have været deaktiveret og genaktiveret igen.

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