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 Oost-Vlaanderen Belgium.
- Assisting with (onsite) training and development
- Supporting the onsite audits
- Assisting with change control activities: tracking, monitoring and reporting on changes
- Validation activities and maintenance of validation documentation
- Taking the lead regarding Health and Safety policies
- Several years of experience in a manufacturing environment
- Understanding of ISO 9001 / PS 9000 / ISO 14001
- Fluent in French and English
- Good prioritizing and time management skills
The Company
Our client is a professional Pharmaceutical organization, based in Flandre Orientale Belgium. They are a specialist in the pharmaceutical manufacturing industry. Their unique view and innovative mindset make sure all can enjoy high quality products.Role Description
You will assist the Quality Manager in the day-to-day running of the Quality Assurance Department. Continuously optimizing resources and planning of manning will be your priority as well as the administration of SOP's. You will be responsible for ensuring that the shifts are ran efficiently and the production levels eventually maximized.Responsibilities
- Complaint handling and internal trend analysis and improvement- Assisting with (onsite) training and development
- Supporting the onsite audits
- Assisting with change control activities: tracking, monitoring and reporting on changes
- Validation activities and maintenance of validation documentation
- Taking the lead regarding Health and Safety policies
Requirements
- BSc. in life science-related field- Several years of experience in a manufacturing environment
- Understanding of ISO 9001 / PS 9000 / ISO 14001
- Fluent in French and English
- Good prioritizing and time management skills
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