Quality Associate
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 Biotechnology and Pharmaceutical organization, based in Oost-Vlaanderen Belgium.
They successfully combine medical research with both academic and pharmaceutical knowledge. Their research and diagnostics department innovatively deliver expertise and quality. They offer general medical for various therapeutic areas.
ROLE DESCRIPTION
You will be part of a team of about a dozen QA professionals that supervise and maintain the quality management system of the company. You will be reporting to the QA Manager and will be responsible for deviations, CAPA and changes, which you partially execute and supervise while also coordinating the planning.
RESPONSIBILITIES
- Safeguarding the Quality Management System and signaling possible problems or deviations
- Follow up on deviations and improvement
- Updating SOPs and procedures
- Management of documentation and training other employees on the use of this
- Participating in project teams in the quality department
- Taking care of the documentation system and preparing of audits
REQUIREMENTS
- BSc. in Pharmacy or Biotechnology/Bioprocessing
- At least 2 years of experience in the pharmaceutical industry in a similar role
- Good knowledge of GMP and the coordination thereof
- Yellow/Green Belt is an asset
- Excellent oral and written English and Dutch communication
- Flexible, team-player
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Amber Moet.
