GMP Coordinator

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Måløv

Do you have a profound knowledge of GMP, and are you motivated by safeguarding our compliance standards and ensuring that we continuously improve our processes and ways of working? Are you excited about the possibility to work with highly qualified colleagues within Quality Control and advanced technology?
If so, you might be our new department GMP Coordinator in Analytical Technology and Innovation in Måløv, Denmark. Apply now and join Novo Nordisk! The position
As the GMP Coordinator for the department, you will collaborate closely with the leadership team and our process responsible. Your primary role will involve supporting both leaders and colleagues in ensuring a high level of Good Manufacturing Practice (GMP).
Work tasks will include, but are not limited to:
  • Driving the preparation for and overseeing the follow-up on authority inspections and internal audits
  • Coaching and assisting your colleagues in GMP-related tasks such as deviations and changes (delimitation, corrective & preventive actions, qualification, etc.)
  • Maintaining a high-level GMP overview and reporting on GMP and quality trends to management
  • Paving the “GMP-way” for new technologies (both hardware robots and software applications)
  • Taking part in managing the department regarding GMP, setting direction, and driving actions and projects across the department

  • Moreover, you will also be a member of the GMP network within the area. In collaboration with your peers in other departments, you will tackle tasks and challenges that span across different areas, such as implementation of new systems or procedures.
    Your job will be characterized by a dynamic blend of coordination, follow-up, and participation in management-related activities, alongside the focused execution of your own tasks. As a result, a flexible workstyle, and the ability to prioritize your tasks and time are essential qualities for this role. Qualifications
    We are looking for someone who proactively takes initiatives and secures commitment from the stakeholders. Our ideal candidate is focused on change management when introducing new ideas.
    To succeed in this role, we expect you to have:
  • BSc or MSc Degree within pharmacy, engineering, or similar field
  • At least 4 years of experience in the pharmaceutical or medical device industry, or a related field, with a specific focus on GMP regulated areas and complex production processes.
  • The ability to think and act with a broad perspective, encompassing the big picture while maintaining focus on and interest in crucial details.
  • Professional proficiency in both Danish and English

  • As an individual, you radiate a positive, cooperative, action-oriented, and solution-focused approach. You work systematically, logically, and proactively. Your effective communication spans all levels of the organization, from operators to management, and you take pride in resolving tasks and challenges with a hands-on approach, involving key stakeholders closely in the process. About the department
    Analytical Technology & Innovation employs approximately 60 highly skilled and motivated employees (laboratory technicians, professionals, and specialists), and we are still growing. Today we are organised in 4 teams. AT&I is supporting Quality Control in Emerging Technologies. We ensure that all laboratory equipment is validated and approved, ready to run relevant analysis. We innovate and build new automated solutions to ensure that our laboratories suit our needs and at the forefront of technology. Working at Novo Nordisk
    At Novo Nordisk, we do not 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, through to Manufacturing, Marketing and Sales – we are all working to move the needle on patient care. Contact
    For further information on the position, please contact Christian Woetmann Lilje at 30750601. Deadline
    17th 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 Måløv.

    Jobbet er oprettet på vores service den 26.2.2024, 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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