Quality & GMP Coordinator

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Hillerød

Do you have passion for GMP, and are you motivated by setting high compliance standards and ensuring that we continuously improve our processes and ways of working? Do you get energy from having a large contact base and the possibility to work with highly qualified colleagues within your field? Then you may be the new Quality and GMP Coordinator we are looking for in Packaging in Hillerød, Denmark. The position As department GMP coordinator, you will work closely with the management team and our Process Responsible. You will be responsible for supporting management and your colleagues in maintaining and developing a high GMP level. As part of your responsibilities, you will:
  • Drive preparation for and follow-up on authority inspections and internal audits.
  • Coach, and assist, your colleagues in GMP related tasks such as deviations and changes (delimitation, corrective & preventive actions, qualification, etc.).
  • Maintain high-level GMP overview, and report on GMP and quality trends to management.
  • Take part in the management of the department with relation to GMP, setting direction, and drive actions and projects across the department.
    • In addition to your tasks in the department, you will also be part of the GMP network within the area, and in corporation with your peers in the other departments, you will address tasks and challenges that go across the areas, such as inspection preparation, implementation of new systems or procedures, etc. Your job will be characterized by a dynamic mix of coordination, follow-up and participation in management related activities and execution of your own task in a more focused manner. Therefore, you must have and be motivated by a flexible workstyle and ability to prioritize your own tasks and time. Qualifications To succeed in this role, we expect you to have:
  • A bachelor or master’s degree within pharmacy, engineering or similar.
  • + 2 years of experience from the pharmaceutical or medical device industry or similar and more specifically from GMP regulated areas and complex production processes.
  • The capacity to think and act with a broad perspective, seeing the big picture without losing sight or interest in important details.
  • Fluency, verbally and in writing, in both Danish and English.
    • As an individual you are positive, cooperative, action and solution orientated, and you work systematically, logically, and proactively. You can interact and communicate at all levels of the organisation, from operator to management, and you take pride in solving your tasks and challenges as close to the process as possible, with close involvement of your key stakeholders. You take initiatives on your own, and you ensure commitment from your stakeholders. You are focused on change management when introducing your ideas. About the department In the department in Hillerød we are responsible for the production and packaging of our Ozempic® and Wegovy® medical devices. While we continuously improve and upgrade our equipment, we are also a launch site with responsibility for implementing and validating new products and production equipment. The position as Quality & GMP coordinator is in our Back Office team with colleagues who are highly engaged and skilled. The team is tasked with complex problem solving which requires deep technical knowledge and high compliance and validation insight. Your colleagues offer expert knowledge and sparring within mechanics, automation, project management, validation, GMP, and compliance. Working at Novo Nordisk Novo Nordisk is its people. We know that life is anything but linear and balancing what is important at different stages of our career is never easy. That’s why we make room for diverse life situations, always putting people first. We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 40,000 employees. Together, we go further. Together, we’re life changing. Contact If you want to know more, please reach out to Julie Sams Agerschou at +45-30752470. Deadline: 8 October 2023. Interviews will be conducted on an ongoing basis; therefore we encourage you 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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    Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".

    Arbejdsstedet er beliggende i Hillerød.

    Jobbet er oprettet på vores service den 16.9.2023, men kan have været deaktiveret og genaktiveret igen.

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