Regulatory Affairs Specialist
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 Pharmaceutical and Biotechnology organisation, based in Netherlands.
- Identify regulatory issues, investigate and suggest solutions
- Provide support regarding regulatory matters for other EMEA franchises and act as a main point of contact
- Manage the release of SKU (codes) restrictions
- Fluency in English. Dutch is a plus.
- Project management skills.
- Previous experience in a Regulatory Affairs position. Pharma, food or medical devices is a plus.
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 Quality & RA Specialist you will support the Regulatory Affairs function in ensuring compliance with national and international guidelines. Together with manufacturers, authorized representatives and global teams you will make sure that the requirements of the Dutch and Belgian legislation are met.Responsibilities
- Ensure regulatory compliance of medical devices regarding to the access to the Benelux market- Identify regulatory issues, investigate and suggest solutions
- Provide support regarding regulatory matters for other EMEA franchises and act as a main point of contact
- Manage the release of SKU (codes) restrictions
Requirements
- Bachelor's Degree in Law, Pharmacy, Biotech or related field.- Fluency in English. Dutch is a plus.
- Project management skills.
- Previous experience in a Regulatory Affairs position. Pharma, food or medical devices is a plus.
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.
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