Director of Technical Operations

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Hillerød

Are you an experienced medical device manufacturing leader who sees the opportunities in leveraging the capabilities of our global network of external partners to support [xxxxx] in scaling our external device manufacturing capacities to reach more patients? Would you like to be part of establishing and building up this new area? Then you might be the Director of Technical Operations we are looking for to join our Global Contract Manufacturing Devices (GCMD) function in Hillerød. Apply today and become part of this exciting journey! The position
As Director of Technical Operations in Global Contract Manufacturing Devices, you will be the owner of all [xxxxx] owned assets and manufacturing processes established at contract manufacturers for components and sub-assemblies for [xxxxx]’s pen systems. The manufacturing processes that the contract manufacturers operate using [xxxxx] owned assets include plastic injection moulding, decoration and assembly and packaging.Some of your key focus include:
  • Heading up a team of currently 8 leaders and approximately 70 employee
  • Establishing and maintaining validated state of [xxxxx] owned equipment at contract manufacturers according to Novo Nordisk’s requirement while leveraging contract manufacturer’s capabilities
  • Identifying and implementing process optimisations across the network to increase throughput and reduce operating cost and/or environmental footprint
  • Asset ownership of [xxxxx] owned equipment at contract manufacturers including life-cycle management to ensure timely handling of obsolescence and reliable supply
  • Technical support and performance optimisation with contract manufacturers
  • Qualifications
    To be considered for this position, we imagine you:
  • Have minimum five years of leading leaders experience with the ability to lead a complex technical organisation
  • Come with solid medical device/GMP value chain understanding and execution
  • Possess a proven track record of creating business results with functional impact
  • Are proficient in English, both spoken and written
  • It would be considered as an advantage if you have experience with outsourcing/external manufacturing or have worked for a contract manufacturer/supplier to other medical device/pharmaceutical companies in production, technical support or quality management. As a person you are not afraid of taking decisions and setting the direction. You are driven, proactive and able to drive empowerment and engagement in a trusting environment. You value diverse perspectives and have a curious and open mindset, which together with your excellent communication and stakeholder management skills allow you to build partnerships with people from different cultures from all parts of the world. About the department
    Global Contract Manufacturing Devices (GCM Devices) is a newly established functional area in [xxxxx] that employs around 200 people. GCM Devices is responsible for all external production of pen needles, components and sub-assemblies for [xxxxx]’s pen systems. GCM Devices manages a network of more than 25 contract manufacturers in Asia, Europe and the Americas, and the expected growth of [xxxxx]’s new drug products is driving the need for more further expansions at existing and new contract manufacturers to reach more patients. Working at [xxxxx]
    At [xxxxx], 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
    For more information, please contact corporate vice president Morten Keller Caspersen at +[xxxxx]. Deadline
    23 August 2024. 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 [xxxxx] 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 Hillerød.

    Jobbet er oprettet på vores service den 2.8.2024, 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.
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