Freelance QA Coördinator
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.
- Development of the QMS (ISO9001, cGMP, ISO17025)
- Manage the deviations and setting up CAPA's
- Review QA related documents on site
- Minimum 3 years of experience in Quality Assurance
- Knowledge of ISOx and cGMP
- Fluent in English and French
Heb je interesse en wil je meer weten over deze functie, reageer dan door op solliciteer te klikken en contact op te nemen met Seppe Verhoeven
The Company
For a service supplier of the biggest pharmaceutical companies in the world, we are looking for a QA Coördinator on site to manage all the QA activities for 2-3 days in the week for 6 months.Role Description
As QA Coördinator, you are responsible for managing all the QA activities on site. You will be in charge to manage all the deviations, CAPA's, documentations, maintaining and developing the QMS and quality oversight. Beside, you will also set up a new training program for the new, permanent QA Coördinator.Responsibilities
- Train and develop a new QA Coördinator- Development of the QMS (ISO9001, cGMP, ISO17025)
- Manage the deviations and setting up CAPA's
- Review QA related documents on site
Requirements
- BsC/MsC in the Life Sciences- Minimum 3 years of experience in Quality Assurance
- Knowledge of ISOx and cGMP
- Fluent in English and French
Heb je interesse en wil je meer weten over deze functie, reageer dan door op solliciteer te klikken en contact op te nemen met Seppe Verhoeven
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