Wash & Sterilisation Professional

Are you well versed in both Wash & Sterilization (W&S) in Aseptic Production? Are you service minded and ready to make your knowledge operational for colleagues worldwide? Would you be excited to support and be part of shaping the future of aseptic manufacturing at Novo Nordisk? 
Then this might be the position for you. Apply today and join us for a life-changing career.

The position
Wash & Sterilization is one of the prerequisites for compliant pharma production. You will play an important role in ensuring compliant and efficient operation of Novo Nordisk aseptic filling facilities world-wide. Your responsibilities will be to support our sites with expert knowledge within both Wash and Sterilization. As a department, we both support running production and new projects. We are responsible for the interaction between production processes and interpretation of external (GMP) requirements.
 

We interpret external (GMP) requirements and ensure global harmonization. As part of this, we support the sites with creation of documentation such as Global SOPs, Change Requests and Deviations.
 

A workday may include: 

Participation in troubleshooting and support in general.  Maintenance of global corporate documents and procedures.  Support in qualification of technologies and improvements across the organization.

You will be cooperating with colleagues from different cultures, with different areas of expertise and at different organizational levels. You will be working out of Søborg, Denmark, but travel may be required. 
There will be plenty of opportunities to take on new responsibilities and grow in this position.
 

Qualifications
To succeed in this role: 

You have a bachelor or master’s degree within Biology, Pharmacy, or equivalent. You have minimum 3 years expertise within both Wash & Sterilization in aseptic production. You have experience within one of these areas, validation/re-validation for sterilization, monitoring, and endotoxin revalidation for cleaning. You may have experience from participation in projects implementing new W&S equipment in aseptic facilities. You have strong analytical and statistical skills. You are well versed in regulatory requirements for W&S.  You have a high sense of quality and know how to handle Quality Management System documentation. You are service minded, goal oriented and a strong team player. You are used to and thrive working in a dynamic environment and can prioritize between many important tasks.  You set a pride in providing excellent support to colleagues.  You are fluent in written and spoken English.

About the department
The Injectable Finished Products (IFP) area produces high-quality products to fight diabetes and obesity worldwide. Site Support & Improvements (SSI) is a dynamic department in IFP Manufacturing Support, supporting our global IFP aseptic production sites and setting the direction for new technologies, innovation, and production optimization globally. We have a strong focus on making a difference in close collaboration with the IFP aseptic production sites, by implementing novel solutions based on data-driven decisions and in accordance with GMP regulations.
 

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