Sr. Project Coordinator
- Regulatory Affairs
- Denmark - Søborg
We are looking for a Senior Regulatory Professional in a temporary position. You have an interest in, and experience with, the development of the design of printed packaging materials, and coordination of labelling launch activities.
About the department
You will join eighteen skilled and motivated colleagues in Regulatory Labelling Development and Launch. The department is responsible for the printed packaging material development and launch projects, where we drive the development of printed packaging material designs for all new Novo Nordisk products and life cycle management projects and we ensure timely market launch of printed packaging materials for all Novo Nordisk products globally.
Regulatory Labelling Development and Launch is part of Regulatory Operations - a VP-area consisting of approx. 140 employees, located in both Denmark and India. The VP-area is responsible for regulatory cross product/project tasks, including labelling development, publishing activities, RA affiliate coordination, IT projects and support to Clinical Trail Applications (CTAs).
The job
As a Senior Regulatory Professional your primary task will be to independently drive projects, both with regards to secondary packaging development and launch activities.
Your job will be to set the right direction for the project and, at the same time, ensure that your project is implemented and anchored in the organisation. The projects will vary in size and complexity, but will all be cross-organisational .
You will be responsible for the following activities:
Preparing, mobilising and running projects;
Ensuring delivery of results according to project plans;
Involving relevant stakeholders;
Communicating/managing change responsibly prior, during and following execution of projects;
Creating, storing, and archiving needed documentation all project activities and decisions thoroughly according to Good Documentation Practices and internal procedures;
Coordinating with relevant functions in NN outside RA.
Qualifications
You have completed a relevant Master's Degree (Masters of Science, Business Administration, Engineering or the like) with excellent results - and have preferably backed your theoretical background with practical experience from the pharmaceutical industry setting. You have acquired solid experience within project management from your involvement in business critical projects. You are comfortable interacting with stakeholders at any organisational level and are used to working across organisational and geographical boundaries.
You are able to work very independently and have a high level of drive, initiative and persistence. You are result-oriented, ambitious, and like to be challenged. You are analytical, structured and comfortable managing a team on your own. You are proficient in Office applications and have an excellent command of our corporate language English. Experience in/with Novo Nordisk is considered a plus.
In Novo Nordisk it is your skills, your commitment and your ambitions, which helps us to improve many people's lives. In return we offer you the opportunity to work with exceptionally talented colleagues, and we offer our employees opportunities for continuous growth.
Contact
For further information, please contact Bente Jessen on +45 3075 8056.
Deadline
16 June 2013.
- Regulatory Affairs
- Denmark - Søborg
We are looking for a Senior Regulatory Professional in a temporary position. You have an interest in, and experience with, the development of the design of printed packaging materials, and coordination of labelling launch activities.
About the department
You will join eighteen skilled and motivated colleagues in Regulatory Labelling Development and Launch. The department is responsible for the printed packaging material development and launch projects, where we drive the development of printed packaging material designs for all new Novo Nordisk products and life cycle management projects and we ensure timely market launch of printed packaging materials for all Novo Nordisk products globally.
Regulatory Labelling Development and Launch is part of Regulatory Operations - a VP-area consisting of approx. 140 employees, located in both Denmark and India. The VP-area is responsible for regulatory cross product/project tasks, including labelling development, publishing activities, RA affiliate coordination, IT projects and support to Clinical Trail Applications (CTAs).
The job
As a Senior Regulatory Professional your primary task will be to independently drive projects, both with regards to secondary packaging development and launch activities.
Your job will be to set the right direction for the project and, at the same time, ensure that your project is implemented and anchored in the organisation. The projects will vary in size and complexity, but will all be cross-organisational .
You will be responsible for the following activities:
Preparing, mobilising and running projects;
Ensuring delivery of results according to project plans;
Involving relevant stakeholders;
Communicating/managing change responsibly prior, during and following execution of projects;
Creating, storing, and archiving needed documentation all project activities and decisions thoroughly according to Good Documentation Practices and internal procedures;
Coordinating with relevant functions in NN outside RA.
Qualifications
You have completed a relevant Master's Degree (Masters of Science, Business Administration, Engineering or the like) with excellent results - and have preferably backed your theoretical background with practical experience from the pharmaceutical industry setting. You have acquired solid experience within project management from your involvement in business critical projects. You are comfortable interacting with stakeholders at any organisational level and are used to working across organisational and geographical boundaries.
You are able to work very independently and have a high level of drive, initiative and persistence. You are result-oriented, ambitious, and like to be challenged. You are analytical, structured and comfortable managing a team on your own. You are proficient in Office applications and have an excellent command of our corporate language English. Experience in/with Novo Nordisk is considered a plus.
In Novo Nordisk it is your skills, your commitment and your ambitions, which helps us to improve many people's lives. In return we offer you the opportunity to work with exceptionally talented colleagues, and we offer our employees opportunities for continuous growth.
Contact
For further information, please contact Bente Jessen on +45 3075 8056.
Deadline
16 June 2013.