Novo Nordisk A/S

GMP supporter

Udløber i dag

Arbejdssted
Hillerød
Oprettet
18. maj 2017
Udløber
28. maj 2017
Ref
85248
Kontakt
Ole Steffensen - Tlf: +45 3079 7728
Jobtype
Fastansættelse

GMP supporter to the world's best packaging lines

This position offers an opportunity to be part of a leading diabetes manufacturing organisation where you will be responsible for setting up new process standards. You will get an exposure to utilise your skills and work closely with internal stakeholders in a global set-up.

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About Department
You will be part of a team consisting of 12 dedicated colleagues. Together we are responsible for a number of high-tech production lines as well as the development and implementation of new lines. This includes that we continuously ensure that we are in compliance with regulatory requirements, and that the production is constantly optimised. In addition, we are responsible for a complex project portfolio, including several new product variants and production lines that will be introduced to the building within the coming years.

We place great emphasis on ensuring that everyone takes personal responsibility for quality, tasks, and each other. We set ambitious goals, focus on stable deliveries and never compromise on quality.

The Position
As part of the DFP (Diabetes Finished Products) team, you will be involved in establishing and implementing Good Manufacturing Practices Support (cGMP) in the packaging area. You will be working in a lively set up of internal stakeholder's thereby interacting and collaborating with one other. You will be responsible to define process structure and finalise SOP (Standard Operating Procedures).You will have to train colleagues to handle presentations, audits and inspections. You will be an integral part to develop new processes and also be responsible for production compliance.

This is a unique opportunity for personal and professional development working in a high performance culture where we take pride in being a great place to work and deliver high impact and value to Novo Nordisk.

Qualifications
You have completed a Master's degree in Science and have at least a minimum of more than 2 years of working experience in medical devices industry. You bring a solid exposure into cGMP and production experience.

You are known for your problem solving & analytical skills, stakeholder management & communication skills, drive & consultant mind-set analytical skills and an international mind-set. As you will cooperate broadly with many stakeholders, you have excellent collaboration and stakeholder management skills and you communicate clearly and concisely. Finally, you work fluently in Danish and 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 Ole Steffensen at +45 3079 7728.

Deadline
28 May 2017.

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