Project Coordinator - Regulatory Affairs
Location: NetherlandsSIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!Our client is a professional Medical Devices organisation, based in Netherlands.
- 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
- 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.
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.
Prosimy o aplikowanie poprzez przycisk znajdujący się po prawej stronie ogłoszenia.
