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GMP Coordinator in Devices & Supply Chain Management

Are you ready for a key role in securing the quality of our products? Then apply for one of our two Maternity cover positions as GMP Coordinator. At Needle and Manufacturing & Sourcing (NMS) you will be challenged and developed in a job characterised by influence and responsibility.

About the department
We are approximately 275 highly skilled employees at Novo Nordisk NMS site in Hjørring. Novo Nordisk is situated very close to the freeway only half an hour drive from e.g. Aalborg and Frederikshavn. We are at the front edge of the development within technology, systems, methods and processes.

The two positions are within our Production Department where the key tasks are moulding, assembly and packaging of approximately 250 million needles a year.

The position
GMP Coordinator for your team is a role of vital importance in our highly regulated industry. Your focus will be to ensure an overall excellent quality level and that quality system and processes meet the requirements from Novo Nordisk and the authorities. You will follow up on quality targets, handle production and quality deviations, optimise procedures and be the central contributor when it comes to ensuring successful inspections and audits in the department. The positions are temporary position of respectively 12 and 18 months with start 1 April 2018 or as soon as possible.

Qualifications
You have a background as Pharmacist, Engineer, Chemist or similar. We are looking for newly graduated as well as more experienced profiles.

Regardless of your expertise you must be able to create changes, set direction and independently drive the cross-functional quality work. You will need a structured approach to problem solving and must thrive in a hectic production environment characterised by many deadlines and ever shifting priorities. In your daily work you will work together with different stakeholders such as operators, specialists, supporters, technicians and managers. This calls for your ability to communicate clearly and concisely in both Danish and English.

Working at Novo Nordisk
At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.

Contact
For further information, please contact Jacob Dam Sørensen at +45 3075 2354 or Bo Henrik Nielsen at +45 3079 5671.

Deadline
18 February 2018.


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329758481Phoenix-e7d1264512018-02-09T17:10:38.133GMP Coordinator in Devices & Supply Chain Management

Are you ready for a key role in securing the quality of our products? Then apply for one of our two Maternity cover positions as GMP Coordinator. At Needle and Manufacturing & Sourcing (NMS) you will be challenged and developed in a job characterised by influence and responsibility.

About the department
We are approximately 275 highly skilled employees at Novo Nordisk NMS site in Hjørring. Novo Nordisk is situated very close to the freeway only half an hour drive from e.g. Aalborg and Frederikshavn. We are at the front edge of the development within technology, systems, methods and processes.

The two positions are within our Production Department where the key tasks are moulding, assembly and packaging of approximately 250 million needles a year.

The position
GMP Coordinator for your team is a role of vital importance in our highly regulated industry. Your focus will be to ensure an overall excellent quality level and that quality system and processes meet the requirements from Novo Nordisk and the authorities. You will follow up on quality targets, handle production and quality deviations, optimise procedures and be the central contributor when it comes to ensuring successful inspections and audits in the department. The positions are temporary position of respectively 12 and 18 months with start 1 April 2018 or as soon as possible.

Qualifications
You have a background as Pharmacist, Engineer, Chemist or similar. We are looking for newly graduated as well as more experienced profiles.

Regardless of your expertise you must be able to create changes, set direction and independently drive the cross-functional quality work. You will need a structured approach to problem solving and must thrive in a hectic production environment characterised by many deadlines and ever shifting priorities. In your daily work you will work together with different stakeholders such as operators, specialists, supporters, technicians and managers. This calls for your ability to communicate clearly and concisely in both Danish and English.

Working at Novo Nordisk
At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.

Contact
For further information, please contact Jacob Dam Sørensen at +45 3075 2354 or Bo Henrik Nielsen at +45 3079 5671.

Deadline
18 February 2018.

2018-02-19T01:04:06.610 Are you ready for a key role in securing the quality of our products? Then apply for one of our two Maternity cover positions as GMP Coordinator. At Needle and Manufacturing & Sourcing (NMS) you will be challenged and developed in a job characterised by influence and responsibility. About the department We are approximately 275 highly skilled employees at Novo Nordisk NMS site in Hjørring. Novo Nordisk is situated very close to the freeway only half an hour drive from e.g. Aalborg and Frederikshavn. We are at the front edge of the development within technology, systems, methods and processes. The two positions are within our Production Department where the key tasks are moulding, assembly and packaging of approximately 250 million needles a year. The position GMP Coordinator for your team is a role of vital importance in our highly regulated industry. Your focus will be to ensure an overall excellent quality level and that quality system and processes meet the requirements from Novo Nordisk and the authorities. You will follow up on quality targets, handle production and quality deviations, optimise procedures and be the central contributor when it comes to ensuring successful inspections and audits in the department. The positions are temporary position of respectively 12 and 18 months with start 1 April 2018 or as soon as possible. Qualifications You have a background as Pharmacist, Engineer, Chemist or similar. We are looking for newly graduated as well as more experienced profiles. Regardless of your expertise you must be able to create changes, set direction and independently drive the cross-functional quality work. You will need a structured approach to problem solving and must thrive in a hectic production environment characterised by many deadlines and ever shifting priorities. In your daily work you will work together with different stakeholders such as operators, specialists, supporters, technicians and managers. This calls for your ability to communicate clearly and concisely in both Danish and English. Working at Novo Nordisk At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth. Contact For further information, please contact Jacob Dam Sørensen at 45 3075 2354 or Bo Henrik Nielsen at 45 3079 5671. Deadline 18 February 2018.11Jobnete7d12645100000000000IDK_OFIR_02DKDanmark228DKK2018-02-18T00:00:000010https://www.novonordisk.com/careers/working-at-novo-nordisk/job-ad-display.52061BR.English.html0EuropaDanmarkEuropaDanmarkSjælland & øerStorkøbenhavnHerlevEuropaDanmarkSjælland & øerStorkøbenhavnFuresøEuropaDanmarkSjælland & øerStorkøbenhavnGladsaxe3106464NOVO NORDISK A/S11Novo Alle 12880Bagsværd30752354DKDanmark0
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