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Hillerød, Denmark Novo Nordisk AS Full timeSelect how often (in days) to receive an alert: Create Alert Do you want to contribute to the continuous improvement of the world’s leading manufacturer of insulin? Do you get motivated by identifying and improving mechanical equipment and business processes for the benefit of millions of patients worldwide? Then this is your chance to be our new Processes...
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Hillerød, Denmark Novo Nordisk AS Full timeCategory: Project Management & Agile Are you interested in helping shape the strategic direction for high-volume manufacturing of new medical devices in internal production? Do you have a strong background in automation and/or decoration, or do you have extensive experience with assembly processes? Then you might be the profile we are looking for in our...
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Hillerød, Denmark Novo Nordisk AS Full timeAssembly and Automation Specialists for Device Production Category: Project Management & Agile Location: Hillerød, Capital Region of Denmark, DK Are you interested in helping shape the strategic direction for high-volume manufacturing of new medical devices in internal production? Do you have a strong background in automation and/or decoration, or do you...
Validation Engineer
1 week ago
About Novo Nordisk
\Novo Nordisk A/S is a leading global healthcare company that drives change to defeat diabetes and other serious chronic diseases. Our company is committed to creating innovative medicines that make a real difference in people's lives.
\The Role
\We are seeking a highly skilled Validation Engineer to join our team at the Site Hillerød production site. As a Validation Engineer, you will play a critical role in ensuring the quality and safety of our products by validating complex manufacturing equipment and processes.
\About the Job
\This position has three main areas of focus:
\- \
- Optimizing existing fully automated packaging lines\
- Ramping up newly implemented automated lines\
- Implementing a new automated packaging line\
- \
In this role, you will work closely with colleagues who offer expert insights in areas such as mechanics, automation, GMP, project management, validation, and compliance. You will be responsible for optimizing and implementing process validation procedures, ensuring adherence to regulatory requirements and industry standards.
\You will have the opportunity to work on various tasks, including optimization, implementation, and documentation, all tied to process validation. Your strong technical understanding of manufacturing equipment, including knowledge of GMP, validation, and computerized systems, will enable you to bridge the gap between the needs of colleagues and automated solutions.
\We are looking for a candidate with a solid technical background, excellent communication skills, and a passion for innovation. If you are motivated by managing complex manufacturing equipment and advancing our technological capabilities, we encourage you to apply for this exciting opportunity.
\About Us
\We are a dynamic company in an even more dynamic industry. We know that what got us here 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're all working to move the needle on patient care.
\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.
