GCP QA Officer
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 Clinical Research and Pharmaceutical organization, based in Brussel Belgium.
It is a CRO that is operating on a international basis.
ROLE DESCRIPTION
AS a GCP QA Officer you will be responsible for the implementation of the revised Quality Management System.
RESPONSIBILITIES
- Participate in the development and implementation of a revised QMS
- Write SOP's, policies & templates (focus on ICH/GCP compliance)
- Prepare and implement CAPA plans
- Assist in the preparation of audits
REQUIREMENTS
- ICH/GCP experience
- Fluent in English
- Experience in writing SOP's
- Able to work independent
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Daniel Woudenberg.