Process Responsible - influence and impact
- Production
- Denmark - Hillerød
Are you a skilled communicator with high-level knowledge within technical processes and GMP? If yes, this could be a grand opportunity for you to pursue your ambitious goals. Join our Support Team on our exciting journey towards enabling short- and long-term success for our production.
About the department
The department consists of approximately 80 employees who daily ensure the assembly of millions of FlexPen® for diabetics around the world. The department is comprised of 2 production teams, 1 technical support team and 1 quality support team. The environment is characterized by fast pace and daily re-prioritizations to ensure timely delivery of quality products to many different customers. There is an open and honest atmosphere in which we aim to utilize and develop your competencies and skills.
The Job
As Process Responsible your overall objective is to ensure high efficiency, stability and quality in our current and future production/processes. You will be responsible for improving and implementing technical processes according to GMP in close dialogue with colleagues at all organisational levels from operators to vice presidents. If deviations occur you will function as sparring partner and expert within your field of knowledge. On site you will be responsible for maintenance for structure, facilitate meetings and in total ensure we make continuous improvements in our processes. You will also assist the team leaders in developing the right competences to meet our goals. Another vital task is to function as sparring partner in developing and aligning processes across production sites globally; therefore you can expect an average of 20 travel days per year.
Qualifications
Your background is a degree in chemical engineering, pharmacy, veterinary science or similar backed by a minimum of 3 years’ experience within a highly regulated industry. Your career has provided you with high evel knowledge about GMP and proves your ability to transform expert knowledge into business performance. As a person, you have an eye for structure and you excel in communicating clearly and constructively, challenging ideas and making decisions while keeping everyone feeling included in the process. Just as important is your ability to establish good relations to a wide number of people across professional and geographical borders. Finally, you must have proficiency in Danish and English, as you will be working in an international environment.
At Novo Nordisk, you will be part of a company respected equally for its financial results and its business ethics. Across geographical, cultural and professional communities we develop and deliver innovative medicines for the benefit of patients.
Contact
For further information, please contact Christian Rank at +45 3075 4929 or Jacob Dam Sørensen at +45 3075 2354.
Deadline
22 December 2013
- Production
- Denmark - Hillerød
Are you a skilled communicator with high-level knowledge within technical processes and GMP? If yes, this could be a grand opportunity for you to pursue your ambitious goals. Join our Support Team on our exciting journey towards enabling short- and long-term success for our production.
About the department
The department consists of approximately 80 employees who daily ensure the assembly of millions of FlexPen® for diabetics around the world. The department is comprised of 2 production teams, 1 technical support team and 1 quality support team. The environment is characterized by fast pace and daily re-prioritizations to ensure timely delivery of quality products to many different customers. There is an open and honest atmosphere in which we aim to utilize and develop your competencies and skills.
The Job
As Process Responsible your overall objective is to ensure high efficiency, stability and quality in our current and future production/processes. You will be responsible for improving and implementing technical processes according to GMP in close dialogue with colleagues at all organisational levels from operators to vice presidents. If deviations occur you will function as sparring partner and expert within your field of knowledge. On site you will be responsible for maintenance for structure, facilitate meetings and in total ensure we make continuous improvements in our processes. You will also assist the team leaders in developing the right competences to meet our goals. Another vital task is to function as sparring partner in developing and aligning processes across production sites globally; therefore you can expect an average of 20 travel days per year.
Qualifications
Your background is a degree in chemical engineering, pharmacy, veterinary science or similar backed by a minimum of 3 years’ experience within a highly regulated industry. Your career has provided you with high evel knowledge about GMP and proves your ability to transform expert knowledge into business performance. As a person, you have an eye for structure and you excel in communicating clearly and constructively, challenging ideas and making decisions while keeping everyone feeling included in the process. Just as important is your ability to establish good relations to a wide number of people across professional and geographical borders. Finally, you must have proficiency in Danish and English, as you will be working in an international environment.
At Novo Nordisk, you will be part of a company respected equally for its financial results and its business ethics. Across geographical, cultural and professional communities we develop and deliver innovative medicines for the benefit of patients.
Contact
For further information, please contact Christian Rank at +45 3075 4929 or Jacob Dam Sørensen at +45 3075 2354.
Deadline
22 December 2013