Quality 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 Biotechnology and Pharmaceutical organization, based in Oost-Vlaanderen Belgium.
Our client is a professional Biotechnology and Pharmaceutical organization, based in Antwerpen Belgium. Our client is a Pharmaceutical Manufacturing Organisation in Belgium.
ROLE DESCRIPTION
- Ensure cGMP Compliance
RESPONSIBILITIES
- Responsible for Inspection Readiness, managing customer audits and authority inspections
- Review quality documents
- Negotiate quality agreements
- Review data of intermediates, API's and deviations
- Collaborate with internal and external parties, coworkers, authorities, clients and suppliers
- Lead external audits
REQUIREMENTS
- Ideally B.Sc. or M.Sc. in Science (Chemistry, Biology, (industrial) Pharmacy)
- Experience in (c)GMP environment
- Fluency in Dutch & Excellent English
- Good communication skills
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.