Qualified Person (2 days per week)
Location: BelgiumSIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science 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!
THE COMPANY
Our client is a professional Pharmaceutical organization, based in Antwerpen Belgium.
The client is a leading international pharmaceutical company concerning with cell processing.
ROLE DESCRIPTION
The client is looking for a QP/RP for two sites in the region of Antwerp for 2 days a week. It concerns a long time contract.In this role you will be responsible that the client products are complaint and in accordance with the applicable directives and laws.
RESPONSIBILITIES
- Compliancy of clients products with applicable directives and law;
- Ensuring proper interactions with the Competent Authorities (CA);
- Keeping up to date with new developments, professional guide-lines and related research;
- Released product in compliance with specifications
REQUIREMENTS
- QP certifified;
- Experience working in Pharma, GMP;
- Knowledge of regulatory systems, biotechnology; more specifically ATMP regulations are a big plus;
- Excellent communication skills in English and Dutch
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Laura Hoekstra.
