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Process Supporter for our New Filling Facility, Kalundborg

Are your analytical skills strong and do you enjoy a hands-on approach to your field? Can you add to the success story of Novo Nordisk and ensure the highest level of quality in the production of life-changing medicine to biopharmaceutical products worldwide? And would you like a range of opportunities for personal and professional development? Then you might be the next member of our dedicated support team.

About the department

In Biopharm, we produce a range of products that help people live with chronical diseases like haemophilia and hormonal imbalances. In our new filling and inspection facility, we will be filling the Active Pharmaceutical Ingredients (API) onto vials and dosage systems. In other words, we make the products ready for packing and distribution with all the processes that are involved in this – from various visual inspections over actual filling procedures to all the documentation that is necessary for us to comply with regulatory and quality standards.

Our filling and inspection facility is ready to enter the next phase, and now we are looking into a period of production ramp up, which in turn initiates many process optimisation projects. You will be part of a support team of dedicated and talented academics and technicians. Our tone is relaxed, and if you enjoy sharing your knowledge and learning from others, you will enjoy working here. The facility is located at our site in Kalundborg with approximately 350 employees.

The position

As process supporter, your primary goal is to ensure that the production consistently delivers a high-quality product in compliance with internal quality requirements and GMP. Our team supports the production on shop floor, and our field of responsibility for the filling processes covers the validation of the lines, the operational procedures to operate them, the expertise in the products and the continuous improvement of the filling lines. This means that whenever something is out of the ordinary, we are the ones who help make everything run again as quickly as possible. When something needs changing, we ensure that the right validation procedures are in place, challenging external vendors on specifications and technical issues when necessary. You will be handling a range of stakeholders with diverse and possibly conflicting needs and concerns in a way that ensures the optimal collaboration across professional and cultural distances – and has the continuation of a stabile production chain as a result.

You will be taking part in systematic problem solving processes, development- and optimisation projects and develop a broad understanding of a complex value chain, when you provide our collective expertise across a truly global organisation. Furthermore, when you are ready, you will support the development of competencies in our production team and participate in audits and inspections.

Qualifications

  • You hold a degree in bio chemistry, bioengineering, automation engineering, or similar.
  • Preferably, you have 2+ years of experience from the pharmaceutical industry after graduating.
  • Knowledge about aseptic production and behaviour as well as current knowledge in process automation in biotech.
  • You have great interest in working with GMP and LEAN.
  • You are fluent in both Danish and English.
     
  • As a person, you are open and honest, independent as well as team player and flexible to changes. You have good communication skills and the ability to efficiently work with concurrent tasks. Being proactive, responsible and energetic is a key to succeed in this position. In return, you will find opportunities for personal and professional development here that will be hard to come by elsewhere.


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