Technology Transfer Team Lead

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Hillerød

Are you ready to make a difference for people living with haemophilia and other rare disorders? Are you passionate about cross-functional teamwork, have deep technical understanding of API production processes, experience with project work and good communication and stakeholder management skills? Then join us as Technology Transfer Team Lead in New Product Entry. The position When joining 25K in Hillerød, you will become part of a dynamic business area which produce API for patients across the world. The department, New Product Entry, is a support function for the API production site 25K in Hillerød. You will join a project focused team with 8 highly dedicated and skilled project managers (five investment project managers, two Technology Transfer Team Leads, and one Project Portfolio Manager) and an associated manager. As Technology Transfer Team lead (T3), your key-responsibility will include:
  • Lead and support API process technology transfer activities for drug candidates, from our development areas into full-scale production for Phase 3 and market launch.
  • Support subject matter experts across a range of different API production related disciplines, to secure timely execution of both pre- and post-campaign activities.
  • Communicate with diverse stakeholders across the entire supply chain (DS, DP, FG) to ensure understanding and adhesion to the overall project- and production-strategies and plans.
  • Improve Technology transfer process and establish project management tools within the department.
  • Furthermore, we expect you to be a natural relation-builder, with excellent collaboration, communication and planning skills, and a holistic mindset to ensure that no dependencies in complex project plans are missed. You will work closely together with the other T3’s in the department, API project directors from the production and CMC areas and representatives from Regulatory Affairs, Quality Assurance, as well as staff at all levels in the API facility. Qualifications To succeed in this role, you have:
  • An academic degree, preferably a master’s degree or a PhD, as an engineer, biochemist, pharmacist or similar or another relevant API technical background
  • A minimum of 5-10 years of experience with API production and/or project management in a GMP regulated environment.
  • Experience with regulatory filing.
  • Strong communication and planning skills.
  • Full professional proficiency in Danish & English.
  • You are a people person with a positive can-do attitude. You work in a structured and proactive way and will never compromise on quality. Good GMP and LEAN understanding is a part of your toolbox. Furthermore, you are able to keep calm and make decisions in a busy work environment where the agenda changes frequently and re-planning is needed. About the department
    API (Active Pharmaceutical Ingredient) Denmark is part of Biotech & Rare Disease (BRD). At our sites in Gentofte, Hillerød, and Kalundborg, we are more than 600 colleagues working together to manufacture the API used in life-saving medicine for people living with serious chronic diseases. We work with advanced chemical and biotechnological processes such as cultivation, recovery, purification, and freeze-drying. We bring value to our patients by providing the cleanest possible high-quality API made in accordance with Good Manufacturing Process (GMP) while constantly optimising our processes. Working at BRD, Novo Nordisk Biotech & Rare Disease (BRD) is part of Novo Nordisk Product Supply , which is a global production network at the forefront of technology and quality production of pharmaceutical products. In BRD, we are not only supplying all Novo Nordisk products to people living with serious chronic diseases, but we also use our competences in biotech to support the growing efforts into completely new production platforms and therapy areas for Novo Nordisk. We are more than 3000 dedicated colleagues working at six production sites in Denmark and the United States. Here we cover the entire production value chain where raw materials are cultivated, purified, formulated, filled, assembled in devices, packed, and distributed across the globe. As more and more people need our products, we support Novo Nordisk's initiatives in new therapy areas. Every day, we work to streamline and expand our capacity through process innovation, automation, and the introduction of new technology . Contact
    For further information please contact Bettina Lundin Brockdorff at +45-34482488 Deadline
    17 September 2023. We will review 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.


    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 22.8.2023, 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.
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