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Novo Nordisk

Technical Writer for Global Process group in Finished Product Production

Fuldtid

Permanent

2880 Bagsværd, Danmark

SE PÅ KORT
ID: 2744314
|
Indrykket for 1 dage siden

Would you like to be a part of shaping the future of manufacturing? Are you motivated by simplifying procedures to make them easy to follow and enjoy being involved in various processes with multiple stakeholders? 
If so, come join us as Technical Writer and make a difference for the global network!
 

Would you like to be a part of shaping the future of manufacturing? Are you motivated by simplifying procedures to make them easy to follow and enjoy being involved in various processes with multiple stakeholders? 
If so, come join us as Technical Writer and make a difference for the global network! 
 
The position 
As a Technical Writer, you will have the responsibility of QMS activities in the department. This involves coordinating and deploying the process for development and maintenance of global QMS standards together with the process managers. You will be working within all Finish Product production processes, delivery processes and the related Q processes.
You will play a key role in our efforts to continuously improve our processes, and you will experience your work having a direct impact on the way we work. You will also become an active sparring partner for the Process Groups and its local participants and have the responsibility to oversee that our QMS system is in control.


Your responsibility will include: 

  • Supporting and guiding process managers and project managers within QMS and change request handling. 
  • Coordinating and supporting the process for updating and developing global standards, i.e. participating in workshops taking the lead on the documentation part.
  • Collaborating with cross-site Process Groups to ensure the incorporation of best practices in the standards.
  • Drafting, structuring, and finalizing documents and related training material in a clear and easy-to-understand language.
  • Overseeing documentation handling in the department. This means having focus on deadlines and quality of the documents.
  • This job is performed in an international environment and hence flexibility to travel is to some extent required.


    Qualifications 
    We are looking for someone who thrives in an ever-changing environment while keeping the high quality of their work. Our ideal candidate enjoys collaborating with various stakeholders from different cultural backgrounds and has a practical knowledge of finished product production.
     
    To succeed in this role, you have:

  • A MSc or equivalent within engineering or similar field. 
  • At least 2 years of experience within Finish Product manufacturing. 
  • Experience within GxP regulated pharmaceutical manufacturing environment. 
  • Professional proficiency in English. 

  • Additionally, you have experience with cLEAN®. As a person you are a team player with a great ability to collaborate. You have a “can-do” attitude and believe that no challenges are too big or too small to handle. You are interested in finding new and improved ways to make our processes more efficient. Furthermore, you are a dedicated professional who is eager to learn and develop new skills.

    About the Department  
    FPM Engineering is a part of Finished Product Manufacturing (FPM) with a team of around 50 colleagues working together to support and optimize processes across all global sites. Our primary responsibility is to drive performance in FPM on all assembly and packaging lines to ensure best practices. In FPM Engineering, we are committed to bringing value to our patients. We do so by supporting all sites with process standardization, ramp-up excellence and technological leadership enabling Novo Nordisk to serve significantly more patients in need of our products.

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