Quality Assurance Specialist
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 Brussel Belgium.
Our client is a service provider to Multinational Pharmaceutical companies
ROLE DESCRIPTION
- In this role you will be responsible for ensuring cGMP compliance on various Pharmaceutical Manufacturing sites.
RESPONSIBILITIES
- Implement and develop the QMS according to cGMP standards at various sites in Belgium
- Promote a QMS according to cGMP standards to local site specialists
- Ensure internal audits GxP at the various sites
- Guide client company audits
- Handle NC and CAPA
- Quality Performance Analysis
- Ensure inspection readiness
REQUIREMENTS
- B.Sc. or M.Sc. (Master or Bachelor) in technical field (e.g. Chemistry, Biology, Pharmacy, or related)
- Dutch, English and French Language skills
- GMP experience
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.