GMP Professional - Måløv, Danmark - Novo Nordisk

    Novo Nordisk
    Novo Nordisk Måløv, Danmark

    Fundet i: Talent DK C2 - for 2 uger siden

    Novo Nordisk background
    Beskrivelse

    Are you passionate about having a central role in a dynamic department with tasks that involve close collaboration with many stakeholders on a daily basis? Do you have a solid understanding of Quality, Good Manufacturing Practice and Training?

    If yes, you might be exactly the one we are looking for to join our team as a Good Manufacturing Practice Professional, apply today

    The Position

    As our new GMP Professional, you will be the department's quality responsible who sets the direction for the department's quality level. You will be a daily sparring partner regarding quality issues, and you will drive quality-related projects in the department. In this role you will lead and coordinate critical quality issues and compliance activities in the department and, if necessary, across.

    Your main tasks will be to:

  • Ensure high-level GMP overview within department.
  • Participate in authority inspections and internal audits.
  • Work in the Quality Management System – Delivery to Quality Management Review (QMR).
  • Support and challenge Deviations (DV) and Changed requests (CR).
  • Responsible for our DV board across the department.
  • Keep track of quality Key Performance Indicator (KPI).
  • Superuser in relevant quality systems.
    • Veeva Vault QualityDocs
    • NovoGlow (NN system)
    • Q-tracker (NN system)

    • You will be part of a network of other GMP and training coordinators in Oral Finished Product (OFP) where you will work with many exciting tasks across the area, such as collaborating with the management team to ensure our quality and training targets are met.


    Qualifications

    We are looking for a GMP Professional who does not compromise on quality and has the drive to set the direction for the department's quality and training level.


    To succeed in this role, you:

  • Have a BSc or MSc in natural science, engineering or similar.
  • Have at least a couple years of experience from pharmaceutical industry or from other regulated areas.
  • Are familiar with complex quality processes and have experience from GMP-regulated areas.
  • Technical understanding of IT and systems, in relation to GMP, is an advantage.
  • Have strong communication skills and like to interact and collaborate with various stakeholders, across departments.
  • Are fully proficient in both Danish and English.

    • Experience with LEAN is an advantage, as it is an integral part of our everyday life.

    As a person you are able to communicate at all levels in the organization and good at solving your tasks pragmatically, also by involving your key stakeholders. It is important that you can think and act with a broad and holistic perspective and see the big picture without losing sight of important details.


    About the department

    OFP is a business area located in two different production buildings which consist of approximately 1000 people. OFP Production & Business Support is a newly established area within OFP Denmark, that consists of approximately 120 people, divided in three departments –Technical Support, Warehouse Support and Business Support.

    We are establishing a new team "Sustainability & Skills" with focus on setting the direction and executing our strategy within Circular for Zero, Health & Safety and training within OFP DK. We have a Triple Bottom Line ensuring focus on environmental and social responsibility as well as economic. We minimize impact on the environment and have a very ambitious environmental strategy with a "Circular for Zero" ambition.

    Working at Novo Nordisk

    At Novo Nordisk, we don't wait for change. We drive it. We are 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 to manufacturing, marketing, and sales – we're all working to move the needle on patient care.


    Contact

    For further information, please contact Associate Manager Charlotte Helene Riggelsen on

    Please notice, that Charlotte isn't the manager for this position, but available for questions.

    Deadline

    25th April 2024.

    Please note that we will be reviewing applications on an ongoing basis, and we encourage you to apply as soon as possible.

    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.