GMP Coordinator

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Gentofte

Denmark - Gentofte Do you get energy from having a large contact base and the possibility to work with highly qualified colleagues within your field? And would you like to combine this with your passion for GMP and serving our patients? Then you may be the new colleague we are looking for in Biotech & Rare Disease QC, Gentofte. About the job You will be responsible for supporting the VP area in developing and maintaining a high cGMP level. The main part of the job will be as GMP Coordinator for the VP area, your key responsibilities will be:
  • Drive and improve processes that create transparency for key quality indicating parameters (Quality Oversight) for example by collecting inputs, preparing and following up on Quality Management Review, and deviation and laboratory investigation reports
  • Identify trends and propose areas where actions should be taken
  • One-point of contact and responsible for coordination of Inspections and Audits on behalf of BRD QC
    • You will have an additional role as GMP coordinator for the Innovation and Business Support department, your key responsibilities will be
  • Supporting the department to maintain sufficient level of compliance with cGMP and Novo Nordisk Quality Management System
  • Support continuous improvements of quality performance and processes by participating in department target setting, identifying continuous improvement opportunities and proposing actions to take
    • In addition to your tasks in the department, you will be part of the GMP network within the area, and in cooperation with your colleagues in the other departments collaborate, align and share better practice of GMP related tasks. Your job will be characterized by a dynamic mix of coordination, follow-up and execution of your own tasks in a focused manner, so you must be able to, and be motivated by, a flexible workstyle and ability to prioritize your own tasks and time. Qualifications
  • You have a background as MSc/BSc within pharmacy, chemical engineering, chemistry/biology or similar, preferably with 2 or more years’ experience from the pharmaceutical or medical device industry or similar related areas.
  • You have experience with authority inspections and audits.
  • You have proven strong skills within GMP and coordination.
  • It’s an advantage if you have experience or knowledge in project management, Lean and/or data systems (Tableau, or similar)
    • As an individual you possess strong collaborative skills and are responsible, goal oriented, timely, systematic and keep a good overview of work in progress, deliverables, etc. You can work with drive and desire to take initiatives and have an appropriate ambition level for improvement of quality performance and processes. Also, you need to be proactive and innovative in relation to problem solving. Adapted to the target group, it is important that you are able to communicate, guide, teach and influence understanding and responsibility for quality and compliance. Novo Nordisk is an international company, so you are fluent verbally and in writing in English. About the Team and the Department The Innovation and Business Support Department is a dynamic and growing department of 35 employees with many interfaces within and outside BRD QC. Our team of 8 employees supports quality and business processes in a QC area of 300 employees, including cGMP compliance, sample forecasting, investment management, and risk management, as well as managing complex QC projects. Contact If you want to know more about the position, please contact Director Rita Herrman at +45 3079 8074. Deadline March 19, 2023 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 Gentofte.

    Jobbet er oprettet på vores service den 21.2.2023, men kan have været deaktiveret og genaktiveret igen.

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