Project Coordinator - Regulatory Affairs
Location: NetherlandsThe Company
This organization is responsible for the manufacturing and distribution of healthcare products all over the world, as well as providing related services for the pharmaceutical, medical devices and diagnostics market.Role Description
As a Project Coordinator you will support the regulatory affairs function in the market access process of medical devices.Responsibilities
- Ensure that all the activities are compliant with local, national and internal regulatory requirements.- Manage different stakeholders and collaborate with Manufacturers, Authorized Representatives and other EMEA locations regarding the Benelux regulations.
- Identify issues in the project scope and solve them adequately.
- Act as the subject matter for any issues related to the project impact within the whole organization.
- Handle the necessary activities for the release of SKU (codes) restrictions
Requirements
- At least a Bachelor's Degree in Law, Biotech, Engineering or similar field.- Excellent communication skills in English
- Experience in project management
- Experience in regulatory affairs in the Food, Pharma or Medical Device industry
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Carla Garcia.
Job Description
The Company
This organization is responsible for the manufacturing and distribution of healthcare products all over the world, as well as providing related services for the pharmaceutical, medical devices and diagnostics market.Role Description
As a Project Coordinator you will support the regulatory affairs function in the market access process of medical devices.Responsibilities
- Ensure that all the activities are compliant with local, national and internal regulatory requirements.- Manage different stakeholders and collaborate with Manufacturers, Authorized Representatives and other EMEA locations regarding the Benelux regulations.
- Identify issues in the project scope and solve them adequately.
- Act as the subject matter for any issues related to the project impact within the whole organization.
- Handle the necessary activities for the release of SKU (codes) restrictions
Requirements
- At least a Bachelor's Degree in Law, Biotech, Engineering or similar field.- Excellent communication skills in English
- Experience in project management
- Experience in regulatory affairs in the Food, Pharma or Medical Device industry
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Carla Garcia.
Additional Information
- Last updated
- Employment type
- Full time
- Contract type
- Self employed
- Number of vacancies
- 1
- Min. experience
- Two years
- Min. education
- Bachelor
- Industry / category
- Jobs in Medicine / Medical service