(Freelance) QA Manager / Brussels North / Pharma / Temporary 2-3 days per week / 6 months project
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 Brussels Hoofdstedelijk Gewest Belgium.
In this role you will be responsible for the implementation of (new) regulations and ensuring compliancy. You will participate in cross-organisational projects, reporting systems and meetings (product maintenance, change controls, deviations, complaints, recall, …). Also you will be responsible for external QA - suppliers and partners directly connected to the manufacturing site (e.g. qualification, audits, quality agreements, evaluation). You promote a good knowledge level in the QA area by setting up a training program for the Quality Unit personnel.
• To implement correct written procedures, in conformity with the internal and international guidelines.
• To guarantee that a good documentation system is in place.
• Participates in the solving of different problems and support for corrective actions in the GxP areas.
• Organisation and performance of Quality Management Review.
• Organisation and performance of self-inspections in GxP relevant areas.
• QA function with respect to external suppliers such as qualification, audits and quality agreements.
• Language skills: English, Dutch and/or French
• Specific and current knowledge of international rules and guidelines for the pharmaceutical industry, Quality Management Systems, GMP & GDP and Regulatory Affairs.
• Experience in a pharmaceutical environment is required
• Autonomous and assume responsibilities
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Martijn van Nieuwenhovensss.
The Company
Our client is a patient-focused, pharmaceutical company committed to bringing Health to people worldwide.Role Description
PROJECT 2-3 days per week for initially 6 months ---In this role you will be responsible for the implementation of (new) regulations and ensuring compliancy. You will participate in cross-organisational projects, reporting systems and meetings (product maintenance, change controls, deviations, complaints, recall, …). Also you will be responsible for external QA - suppliers and partners directly connected to the manufacturing site (e.g. qualification, audits, quality agreements, evaluation). You promote a good knowledge level in the QA area by setting up a training program for the Quality Unit personnel.
Responsibilities
• To prepare and review the documents linked to the implementation of the Quality Policy and the Quality Management System (SOPs, WI’s…).• To implement correct written procedures, in conformity with the internal and international guidelines.
• To guarantee that a good documentation system is in place.
• Participates in the solving of different problems and support for corrective actions in the GxP areas.
• Organisation and performance of Quality Management Review.
• Organisation and performance of self-inspections in GxP relevant areas.
• QA function with respect to external suppliers such as qualification, audits and quality agreements.
Requirements
• Education and on the job experience: Min. 3 years of experience as Quality Assurance Officer or Manager• Language skills: English, Dutch and/or French
• Specific and current knowledge of international rules and guidelines for the pharmaceutical industry, Quality Management Systems, GMP & GDP and Regulatory Affairs.
• Experience in a pharmaceutical environment is required
• Autonomous and assume responsibilities
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Martijn van Nieuwenhovensss.
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