Skilled Regulatory Affairs Manager

Modis Life Science is now looking for a consultant for an assignment as Regulatory Affairs Manager at a pharmaceutical company in Uppsala. As a consultant you will be hired by Modis. 

The customer is a well-known global pharmaceutical company and we are now looking for a skilled Regulatory Affiairs Managar for thisassignment, initially running for 8 months. 

Essential duties and responsibilities in the role:

• Local support to the project leaders and related communication to all stakeholders.
• Support regulatory compliance of Medical Devices (MD) for all Markets
• Identify Regulatory Issues & strategies concerning MD, in the scope of the Project investigate and suggest solutions to resolve them.
• Provide regulatory support to ensure consistent collaboration with franchises and EMEA/ Regulatory Affairs, and act as the main contact person for any matters related to the Project impact issues.

To succeed in this role you need:

• Relevant academic backround
• 5 years of relevant experience working with regulatory affairs and technical files
• Advanced skills in excel

If you find the role interesting apply as soon as possible, no later than November 10th. For questions, please contact cecilia.larzon@modis.se