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Engineer/Pharmacist for Packaging Development

Are you an engineer or pharmacist with experience from packaging development? Are you ready to take responsibility for the quality specifications for the packaging of the best drugs and delivery devices on the market? Then join Device Manufacturing Development as Secondary Packaging Quality Engineer for Novo Nordisk.

About the department

Join a team of dedicated and highly competent colleagues and be at the crossroad between Device Research & Development (R&D) and production. The department supports the entire range of Novo Nordisk device products, and the technical product knowledge is anchored here.

The department is responsible for the design, risk documentation, specifications, quality requirements under GMP and test methods for the secondary packaging of our marketed products.

The position

As a Secondary Packaging Quality Engineer/Pharmacist for Product Maintenance, you own and develop quality specifications for the packed products, and associated test methods. These specifications secure, that the packed product has the required high quality to be released and are vital to ensure that Novo Nordisk delivers quality product to customers all over the world.

You will work with products under development as well as marketed products. You respond to inquiries from stakeholders all over the world and support, when quality issues arise. You update quality specification documentation and release method documentation, and you participate in optimization projects.

You can look forward to a position, where your work has a high impact on the end products, that reach the patient, and the packaging processes leading to this. The job gives you a great opportunity for working with innovative products on an international level and for having a broad range of contacts including production sites globally, R&D, Quality Assurance, regulatory affairs, customer service and affiliates.


Our expectations:

  • You hold an engineering, pharmacist degree or similar.
  • You have solid experience within packaging in the pharmaceutical industry and with Good Manufacturing Practice (GMP).
  • You are highly skilled with MS Office and find it easy to master new IT systems.
  • Your language proficiency in both written and spoken English is at a professional level as most of your tasks will be executed in collaboration with colleagues in e.g. US, Brazil, China, France, Russia, Algeria and Japan.
  • As a person, you are good at keeping an overview of your tasks and handling a large amount of data and documents. You are quality-conscious, and you are known for a high commitment to finding constructive solutions. You perform well in a team-oriented environment, and you also enjoy working independently. Success in this role requires, that you make decisions regarding quality tasks and find the right balance between quality demands, authority demands and business needs.

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