Chemist
- IT
- Denmark - Kalundborg
Are you looking for a career opportunity where you unfold your skills within the workflow process of the IT & Automation team in IM2 Kalundborg.We are on the lookout for a person with strong focus in the documentation process, with the right quality mind set and personal drive. Anticipate a challenging job where you make us even better at fighting diabetes through your impact on our standards and processes.
About the department
You will join a team of 17 employees and the almost 500 employees of Insulin Manufacturing 2 (IM2) in Kalundborg. The team has a wide variety of responsibility areas relate to IT and automation systems. For instance system maintenance, process improvements, project execution, support and guide to the factories in IM2
The Job
Standardization and support.You will be responsible for anchoring a strong culture of standardization within the Business Support department 805.03 and working across the site. In close cooperation with the Team Manager and the team, you will ensure drive, preparation and completion of various qualification tasks carried out in the team. You will ensure systematic and well-coordinated GMP level in our change requests, non-conformities, qualification initiatives and GMP awareness in general in the team.In the future, you will be the local super user of NN´s electronic qualification tool called e-TIMS. You will ensure the future role out preparations and usage in IM2
Qualifications
Academic background – Solid GMP experience – knowledge of production and IT.You have a relevant degree at bachelor/master’s level, which you have combined with solid GMP experience. If you have IT or PCS knowledge, this will be an advantage in completion of the daily tasks.Your personal qualities define you as structured, self-starting and capable of finalizing tasks with a high level of quality mind set. In your daily challenges you have the personal skills of listening and understanding complex circumstances, subsequently define necessary arrangements and set direction with the right level of GMP focus. Everything is done in close cooperation with team- or department representatives.In addition, you have the ability of understanding a variety of process computer systems and the data consistency within.Last but not least, you have proficiency in writing various documents related to quality activities within the area of responsibility of the team. Documents will be prepared in Danish most of the time.
Novo Nordisk in Kalundborg is a city within the city. The area is situated approximately 1 hour from Copenhagen and covers 1,350,000 m2. We produce some 50 % of the insulin in the world. We are at the front edge of the development within technology, systems, methods and processes. If you are our new colleague, we can guarantee opportunities that you will have a hard time finding anywhere else.
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 Uffe Nybro Jensen at +45 3075 0036.
Deadline
26 June 2013
- IT
- Denmark - Kalundborg
Are you looking for a career opportunity where you unfold your skills within the workflow process of the IT & Automation team in IM2 Kalundborg.We are on the lookout for a person with strong focus in the documentation process, with the right quality mind set and personal drive. Anticipate a challenging job where you make us even better at fighting diabetes through your impact on our standards and processes.
About the department
You will join a team of 17 employees and the almost 500 employees of Insulin Manufacturing 2 (IM2) in Kalundborg. The team has a wide variety of responsibility areas relate to IT and automation systems. For instance system maintenance, process improvements, project execution, support and guide to the factories in IM2
The Job
Standardization and support.You will be responsible for anchoring a strong culture of standardization within the Business Support department 805.03 and working across the site. In close cooperation with the Team Manager and the team, you will ensure drive, preparation and completion of various qualification tasks carried out in the team. You will ensure systematic and well-coordinated GMP level in our change requests, non-conformities, qualification initiatives and GMP awareness in general in the team.In the future, you will be the local super user of NN´s electronic qualification tool called e-TIMS. You will ensure the future role out preparations and usage in IM2
Qualifications
Academic background – Solid GMP experience – knowledge of production and IT.You have a relevant degree at bachelor/master’s level, which you have combined with solid GMP experience. If you have IT or PCS knowledge, this will be an advantage in completion of the daily tasks.Your personal qualities define you as structured, self-starting and capable of finalizing tasks with a high level of quality mind set. In your daily challenges you have the personal skills of listening and understanding complex circumstances, subsequently define necessary arrangements and set direction with the right level of GMP focus. Everything is done in close cooperation with team- or department representatives.In addition, you have the ability of understanding a variety of process computer systems and the data consistency within.Last but not least, you have proficiency in writing various documents related to quality activities within the area of responsibility of the team. Documents will be prepared in Danish most of the time.
Novo Nordisk in Kalundborg is a city within the city. The area is situated approximately 1 hour from Copenhagen and covers 1,350,000 m2. We produce some 50 % of the insulin in the world. We are at the front edge of the development within technology, systems, methods and processes. If you are our new colleague, we can guarantee opportunities that you will have a hard time finding anywhere else.
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 Uffe Nybro Jensen at +45 3075 0036.
Deadline
26 June 2013