Quality Assurance Officer
Location: BelgiumSIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences 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!Our client is a professional Pharmaceutical organisation, based in Antwerpen Belgium.
- Provide game plans for unforeseen activities on the manufacturing site
- Review and assessment of QA
- GMP compliance and the review and development of established and new procedures
- Risk / impact assessment
- +2 years of experience in a pharmaceutical environment
- Experience with GMP
- Quality Assurance 3rd level degree
- Some quality Management experience is an asset
- Fluent in English and Dutch, Good knowledge of French
The Company
They are immensely active on the global pharmaceutical market and invest in clinical trials. They aim for thorough research and manufacturing of general medicine.Role Description
You will be functioning in the Quality Assurance team, where you will be responsible for the QA support of manufacturing sites. You will be reporting to the QA manager and support the day-to-day activities of the Quality Assurance department.Responsibilities
- Review of batch release documentation- Provide game plans for unforeseen activities on the manufacturing site
- Review and assessment of QA
- GMP compliance and the review and development of established and new procedures
- Risk / impact assessment
Requirements
- BSc. in life science related field- +2 years of experience in a pharmaceutical environment
- Experience with GMP
- Quality Assurance 3rd level degree
- Some quality Management experience is an asset
- Fluent in English and Dutch, Good knowledge of French
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