GMP Engineer for IT/automation
- IT
- Denmark - Kalundborg
Are you looking for a career opportunity where you can combine your GMP and project management skills with your flair for IT systems? Anticipate a challenging job where you make us even better at fighting diabetes through your impact on our standards and processes.
About the department
Insulin Manufacturing 2 (IM2) with its 500 employees is one of three production units in Novo Nordisk’s insulin production (DAPI) which delivers insulin to the global market. The primary production capacity in IM2 consists of three plants: fermentation, recovery and purification. As part of IM2’s Business Support which solves a wide range of tasks for the production, the IT & Automation team is responsible for areas such as process improvements, project execution and system maintenance and support to the factories in IM2.
The job
You will through your GMP knowledge and expertise proactively ensure that the efforts of the developers in IT & Automation match the GMP requirements. This means that you will ensure a systematic and well-coordinated GMP level in our change requests, non-conformities, qualification initiatives and GMP awareness in general in the team. You will be responsible for anchoring a strong culture of standardization within the Business Support department and also work across the Insulin Manufacturing 2 site as the key driver of projects such as consolidating local automation systems, simplifying the HW landscape and contributing to the future upgrades of various installations in close cooperation with the team. You will drive the preparation and completion of various qualification tasks carried out in IT & Automation, and ensure the future roll-out preparations and usage of NN´s electronic qualification tool called e-TIMS in IM2, as it is expected that you will become the local super user.
Qualifications
We are on the lookout for a person with a strong focus in the documentation process and personal drive. You have a relevant degree at bachelor/master’s level, for example in chemical or production engineering, which you have combined with solid GMP experience. If you have IT or Process Control System knowledge, this will be an advantage. Your personal qualities define you as structured, self-starting and capable of finalizing tasks with a high-level quality mind-set. You are able to understand complex issues, and subsequently define necessary arrangements and set direction with the right level of GMP focus. In addition, you have the ability to understand 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. www.novonordisk.com/kalundborg-careers
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
22 September 2013.
- IT
- Denmark - Kalundborg
Are you looking for a career opportunity where you can combine your GMP and project management skills with your flair for IT systems? Anticipate a challenging job where you make us even better at fighting diabetes through your impact on our standards and processes.
About the department
Insulin Manufacturing 2 (IM2) with its 500 employees is one of three production units in Novo Nordisk’s insulin production (DAPI) which delivers insulin to the global market. The primary production capacity in IM2 consists of three plants: fermentation, recovery and purification. As part of IM2’s Business Support which solves a wide range of tasks for the production, the IT & Automation team is responsible for areas such as process improvements, project execution and system maintenance and support to the factories in IM2.
The job
You will through your GMP knowledge and expertise proactively ensure that the efforts of the developers in IT & Automation match the GMP requirements. This means that you will ensure a systematic and well-coordinated GMP level in our change requests, non-conformities, qualification initiatives and GMP awareness in general in the team. You will be responsible for anchoring a strong culture of standardization within the Business Support department and also work across the Insulin Manufacturing 2 site as the key driver of projects such as consolidating local automation systems, simplifying the HW landscape and contributing to the future upgrades of various installations in close cooperation with the team. You will drive the preparation and completion of various qualification tasks carried out in IT & Automation, and ensure the future roll-out preparations and usage of NN´s electronic qualification tool called e-TIMS in IM2, as it is expected that you will become the local super user.
Qualifications
We are on the lookout for a person with a strong focus in the documentation process and personal drive. You have a relevant degree at bachelor/master’s level, for example in chemical or production engineering, which you have combined with solid GMP experience. If you have IT or Process Control System knowledge, this will be an advantage. Your personal qualities define you as structured, self-starting and capable of finalizing tasks with a high-level quality mind-set. You are able to understand complex issues, and subsequently define necessary arrangements and set direction with the right level of GMP focus. In addition, you have the ability to understand 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. www.novonordisk.com/kalundborg-careers
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
22 September 2013.