Assembly and GMP specialist
- Production
- Denmark - Hillerød
If you posses a high level knowledge within assembly and GMP, you are just the person we are looking for. You can look forward to a great diversity of tasks while working across production and development.
About the department
You will join Pre-assembly Production. We are approx. 65 colleagues in 5 teams and we produce the mechanical motor module in Novo Nordisk’s newest prefilled devices FlexTouch® and FlexPro®. We deliver large quantities to our sister factories in Diabetes Finished Products and Biopharmaceuticals. The department also handle improvements, upgrades and new pen systems with a global production perspective.
The job
As Assembly & GMP Specialist your overall objective is to ensure high efficiency, stability and product quality on current and future production equipment. Your role makes you an important member of the process group where we prioritise and decide on solutions for improvement projects. You will be responsible for the contact between Device Manufacturing Development and the Pre-assembly Production and focus on feasibility studies for the future implementation of new pen systems or changes to the existing. You support technical improvements within the field of mechanics, vision, automation and processes for solutions in-house as well as at supplier sites. Other vital tasks are to support, challenge and improve the department’s GMP as well as support, improve and share knowledge within the risk based validation setup. We have a new fully automated assembly line in schedule and you will play an important role in the implementation of this. You will also contribute in audits presenting your areas of expertise.
Qualifications
Your background is engineering degree backed by a minimum of 5 years’ experience within the industry where you have worked with vision and automation and gained experience within project management. Your career has provided you with a solid knowledge within assembly, pharmaceutical device production and GMP. This includes highlevel knowledge within validation, preferably with a riskbased approach. You work with curious approach and are able to spot weaknesses in equipment, processes, systems and methods and improve these in a close dialogue with your colleagues. To succeed you must be able to plan and execute your tasks very independently. Just as important is your ability to establish good relations to a wide number of contacts across professional borders – Operators, Technicians, Engineers as well as other departments e.g. Quality Assurance, Logistics and Device R&D. This takes diplomacy, communication and networking skills.
At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.
Contact
For further information, please contact Johnny Bertelsen at +45 3075 1311.
Deadline
5 August 2013
- Production
- Denmark - Hillerød
If you posses a high level knowledge within assembly and GMP, you are just the person we are looking for. You can look forward to a great diversity of tasks while working across production and development.
About the department
You will join Pre-assembly Production. We are approx. 65 colleagues in 5 teams and we produce the mechanical motor module in Novo Nordisk’s newest prefilled devices FlexTouch® and FlexPro®. We deliver large quantities to our sister factories in Diabetes Finished Products and Biopharmaceuticals. The department also handle improvements, upgrades and new pen systems with a global production perspective.
The job
As Assembly & GMP Specialist your overall objective is to ensure high efficiency, stability and product quality on current and future production equipment. Your role makes you an important member of the process group where we prioritise and decide on solutions for improvement projects. You will be responsible for the contact between Device Manufacturing Development and the Pre-assembly Production and focus on feasibility studies for the future implementation of new pen systems or changes to the existing. You support technical improvements within the field of mechanics, vision, automation and processes for solutions in-house as well as at supplier sites. Other vital tasks are to support, challenge and improve the department’s GMP as well as support, improve and share knowledge within the risk based validation setup. We have a new fully automated assembly line in schedule and you will play an important role in the implementation of this. You will also contribute in audits presenting your areas of expertise.
Qualifications
Your background is engineering degree backed by a minimum of 5 years’ experience within the industry where you have worked with vision and automation and gained experience within project management. Your career has provided you with a solid knowledge within assembly, pharmaceutical device production and GMP. This includes highlevel knowledge within validation, preferably with a riskbased approach. You work with curious approach and are able to spot weaknesses in equipment, processes, systems and methods and improve these in a close dialogue with your colleagues. To succeed you must be able to plan and execute your tasks very independently. Just as important is your ability to establish good relations to a wide number of contacts across professional borders – Operators, Technicians, Engineers as well as other departments e.g. Quality Assurance, Logistics and Device R&D. This takes diplomacy, communication and networking skills.
At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.
Contact
For further information, please contact Johnny Bertelsen at +45 3075 1311.
Deadline
5 August 2013