CMC Project Director

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Are you looking for an exciting opportunity within Project Management, where you will lead complex projects through the Chemistry, Manufacturing & Control (CMC) development process to the approval stage? Do you want to deliver visible footprints and utilise your excellent leadership skills by setting the direction and motivate your cross functional project teams within CMC development? If yes, then the CMC Project Director position might be just the right career move for you. Come join us, apply today! The Position You can look forward to a broad range of exciting challenges that have senior management attention feeding into your personal and professional development. With direct reference to a Portfolio Vice President (PoVP) you will manage CMC projects during the development phases ensuring efficient transfers from Global Research Technologies to CMC Development and later to Product Supply.   Your main responsibilities will be:
  • Project Management - managing the development of product and manufacturing processes, securing timely supply to non-clinical and clinical studies as well as providing the corresponding documentation to Health Authorities.
  • Stakeholder Management – developing strong internal and external networks. Interact with internal stakeholders as well as external parties (e.g., Contract Manufacturing Organisations and Health Authorities).
  • Project Team – managing, supporting and motivating the cross functional CMC Core Teams involving all relevant CMC disciplines.
  • Strategy Execution - preparing and executing on the CMC development strategy and plan incl. project scenario building and risk management
  •   Our working environment is flexible, dynamic and informal with a strong culture of cross-functional collaboration, where your contributions will be valuable and make a difference. We are committed to digitalisation and automation and see these as key enablers to reach our strategic aspirations.   Qualifications To thrive in this role you
  • Hold a Master or PhD degree within a relevant field of scientific expertise such as Chemistry, Chemical Engineering, Pharmacy, Biology or similar
  • Possess solid knowledge of the CMC value chain, as well as drug development and regulatory requirements. You have several years (+5 years) of experience in successful project management from R&D or Manufacturing Development
  •   As a person you:
  • have excellent collaboration and communication skills. You are a talent in engaging and motivating teams with diverse backgrounds and communication in a clear way
  • set a clear direction, solve complex tasks and create overview in relation to business strategies and project scope with a curious and structural approach
  • display a high level of independence, personal engagement, drive to reach results as well as integrity
  • find it rewarding to work towards reaching your own project’s goals while also engaging in activities across projects
  • are fully proficient in both written and spoken English.
  • About the department CMC Portfolio Management is part of CMC Development. CMC Development is the link between research and production supplying products needed for all of Novo Nordisk’s clinical trials around the world. We develop, manufacture, and distribute drug candidates for clinical trials and develop commercial manufacturing processes and technologies with consistent scientific documentation for drug approval.   In CMC Portfolio Management, we are responsible for all CMC development projects. All the way from lead drug candidate selection, throughout phase 1, 2 and 3 clinical development to regulatory submission and project transfer to commercial manufacturing. The department is the link between CMC Development and stakeholders across Novo Nordisk but also to relevant external partners.   You will join a dedicated team of Project Directors all responsible for their own project portfolio.   Working at Novo Nordisk At Novo Nordisk, 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 questions, please contact CVP of CMC Portfolio Management, Camilla Schmidt, at: +45 3079 5479.    Deadline 25 August 2023. Interviews will be conducted on an ongoing basis, so please apply today.   You do not need to attach a cover letter to your application, but please include a few lines about your motivation in your resume or CV. In addition, please avoid the use of photos in your CV. This makes for a better and more fair process. 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 "Administrativ medarbejder", og befinder sig i kategorien "Kontor, handel og service".

    Arbejdsstedet er beliggende i Bagsværd.

    Jobbet er oprettet på vores service den 18.7.2023, 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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