GMP Partner

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Gentofte

Are you passionate about compliance, continuous improvements, working with a wide stakeholder landscape and having influence on results? Are you self-motivated, structured and have the ability to see and develop innovative solutions in a broader perspective? Then you are the candidate we are looking for! The Position As our new VP GMP partner you will proactively support the BRD QC area to maintain a high level of quality and compliance. You will do this by working closely with many colleagues and management across BRDQC departments, as well as QA, QC and compliance partners in other areas of BRD and NN. In this position, you will be responsible for:
  • S upporting the organisation to maintain sufficient level of compliance with cGMP and NN QMS.
  • Developing and maintaining systems to monitor and create transparency for key quality indicating parameters (Quality Oversight), identify trends, propose and support the organisation to develop relevant actions.
  • Supporting continuous improvements of quality performance and processes by participating in target setting, identification of continuous improvement opportunities and proposing actions to take.
  • Ad hoc sparring, collaboration, consultation, sharing within and outside BRD QC on quality and compliance improvement ideas and challenges.
    • As part of your main responsibilities, you will maintain an effective and efficient GMP network with the purpose to collaborate, align and share best practices for GMP related tasks across BRD QC. Qualifications To succeed in this role, you have:
  • An Academic degree: Master of Science, Master of Science in Engineering, Master of Science in Pharmaceutical Sciences or equivalent.
  • +5 years of relevant experience in a similar role within a GMP regulated environment.
  • Experience from the pharmaceutical industry is an advantage.
  • Advantageous to have experience or knowledge in Project Management, Lean.
  • Excellent interpersonal skills and proven experience in working with stakeholders at all levels.
  • Fluency in spoken and written English
    • On a personal level you thrive and get motivated by working with and across all levels in the organisation, whilst you are known for your excellent collaboration and communication skills and ability to set direction, teach and influence. In addition to your natural ability to work independently, you are solution oriented and work systematically, proactively and strive for simplicity in processes, while taking pride in solving your tasks and challenges as close to the process as possible, with close involvement of your stakeholders. About the Department Your role will be anchored in BRD QC Innovation and Business Support Department . We are approximately 40 colleagues supporting six departments across BRD QC in business support processes such as Training, Admin, Forecast, Planning, GMP, Data management and GlobalLIMS; as well as management of various Innovation and Technology projects. Working at 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 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. 2650 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 also strive 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? Contact For further information please contact Rita from the 14th of August on phone +45-30798074. Deadline 20 August 2023. Applications will be screened on an ongoing basis, so you are encouraged to apply as soon as possible. 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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    Arbejdsstedet er beliggende i Gentofte.

    Jobbet er oprettet på vores service den 1.8.2023, men kan have været deaktiveret og genaktiveret igen.

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