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Filling Professional with Experience from Aseptic Production

  • Manufacturing
  • Hillerød   

Are you ready to take on new and exciting challenges as part of the Filling support team in Diabetes Finished Products (DFP)?

Do you have a science degree, some experience from pharma and know what it takes to work in compliance with standard procedures in an GMP regulated environment?

If so, this is your opportunity to join the AP Expansion project at our site in Hillerød.


About the department
You will be part of a filling support team of 10-12 experienced and highly engaged process supporters which is responsible for validation, operation and re-qualification of our two brand new isolator filling lines.

 

The APX project was launched in 2015 to build a completely new filling factory designed to fill insulin cartridges using state of the art filling technology for a wide range of Novo Nordisk products. At this point, we are finishing the last validation and qualification activities on the filling lines with the aim of producing for the market in 2020.

 

Our department manages our two filling lines as well as all related equipment and processes. Daily department activities include creating standards, validating processes and equipment, handling deviations and ensuring that we have procedures in place for production. We work across departments and cultures and always strive to deliver best in class support to our customers.

The position
As a filling professional your responsibilities include optimising processes and procedures, deviation handling, project execution, validation activities and getting regulatory approvals, all in accordance with quality and compliance.

As a facility we are developing new processes and optimizing daily work using cLEAN as our primary tool. The team consist of a wide range of competences which gives the right candidate opportunities to develop skills within a variety of fields of expertise.

 

You will be involved in maintaining a high level of compliance and work with regulatory approvals of the filling equipment and processes by ensuring correct documentation and being inspection ready at all times.

 

Qualifications
You have a relevant science degree such as engineering, pharmaceutical or similar and at least a couple of years’ experiences from the medical industry.

Preferably you have at least a few years’ experience within aseptic filling processes and equipment and have worked with processes in a cGMP environment. You understand the regulatory environment and ensuring compliance comes as second nature.

 

You have worked with validation and documentation processes before and have experience with writing protocols, test plans, deviations, change request cases and SOPs.

 

You work in a structured manner, systematically with an eye for details and with changing priorities can manage hands-on tasks as well.

Your hands-on experience has sharpened your already good communication and coordination skills and through your “can do” attitude you make things happen. You are highly skilled at communicating at all organisational levels - with operators, managers and specialists - verbally as well as in writing.

 

Finally, you have good skills in verbal and written English


Working at Novo Nordisk
At Novo Nordisk, we use our skills, dedication and ambition to help people with diabetes. We offer the chance to be part of a truly global work place, where passion and engagement are met with opportunities for professional and personal development

Contact
For further information, please contact Julie Degn Nielsen +45 3079 4927 or Steffen Elholm Andersen on +45 3079 4709

Deadline
17th february 2020.

 

Millions rely on us
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.
 


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