CVP GMP Partner

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Gentofte

Are you passionate about compliance, structure, and continuous improvement, and possesses a self-motivated, structured, and efficient nature? We are on the lookout for an experienced candidate with proven track record of identifying solutions in a broader perspective and setting clear direction and have demonstrated a commitment to making a significant difference.
Apply now and join our team as CVP (Corporate Vice President) GMP Partner within Biotech and Rare Disease (BRD) based in Gentofte!
The position
As our new CVP GMP Partner, you will be a part of BRD, Finished Production (FP) management group, referring to the CVP. You will be responsible for supporting the departments within BRD FP to ensure they are continuously improving compliance and delivering on all relevant GMP requirements.
You will also play an important role of supporting the GMP coordinators to ensure a high level of quality and compliance in our FP areas in Gentofte, Kirke Værløse and Kalundborg by setting high standards, identifying, scoping, and driving compliance improvement initiatives while maintaining our Quality Management System (QMS).
You will be responsible for:
  • Coordinating preparation for audits and inspections, including planning, organisation and execution and follow-up, providing ad hoc consultation on quality and compliance improvement ideas and challenges.
  • Supporting compliance with GMP and NN QMS.
  • Developing and maintaining quality oversight systems to identify trends and propose relevant actions.
  • Ensuring high-level GMP overview and reporting quality trends to management.
  • Driving continuous improvement of quality performance and processes.
  • Ensuring the maintenance of a productive and efficient GMP coordinators network, which will facilitate collaboration, alignment, and the sharing of best practices for GMP-related tasks across BRD FP.
  • Qualifications
    Your experiences include:
  • A degree in a scientific field such as Pharmacy, Sciences, Engineering, or relevant.
  • 5+ years of experience in a similar position within pharma GMP production.
  • Experience within Finished Production/ QA is advantageous including Quality Management Review.
  • Audits and inspections.
  • A LEAN mindset with experience in systematic problem-solving.
  • Full proficiency in oral and written English.
  • As a person, you have excellent interpersonal and collaboration skills with the ability to set direction. You thrive solving tasks and challenges as close to the process as possible and working cross functionally with stakeholders at all levels.
    You are solution-oriented, and you work systematically and proactively while striving for simplicity in processes. You take thrive solving tasks close involvement of your stakeholders. About the area
    BRD is part of Novo Nordisk Product Supply, which is a global production network at the forefront of technology and in quality production of pharmaceutical products. In BRD we are not only supplying all Novo Nordisk products for Rare Diseases, but also using our competences in Biotech to support the growing efforts into completely new production platforms and therapy areas for Novo Nordisk. We are app. 2500 colleagues committed to drive change for people with serious chronic diseases. We produce our life-saving medicines out of five state-of-the-art production sites in Denmark and United States - covering the entire production value chain where raw materials are cultivated, purified, formulated, filled, assembled in devices, packed, and distributed across the globe. Not only are we making a difference for patients – we are also stiving to make a difference for our employees by promoting a learning culture with high level of trust, innovation, and development for everyone. Are you ready for a life-changing career?
    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 necessary 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
    To learn more about this opportunity please call, Rasmus Herschend (Senior Manager, Gentofte Packaging): +45 3079 7717 or Sune Mohr (CVP, BRD Finished Products GE & VA): +45 3079 9891
    Deadline
    17 March 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 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 Gentofte.

    Jobbet er oprettet på vores service den 1.3.2024, 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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