QA Officer Consultant
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 Bruxelles-Capitale Belgium.
- batch review
- Batch releases
- GMP regulations
- Validation
- CAPA
- Deviations
- SOP's
- Taking initiative
- Team Player
- Hands on mentality
- At least 1 year of experiences within the QA
- Experience with a GMP / manufacturing environment
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Amber Moet.
The Company
Their ambition is to transform the lives of people living with severe diseases. They focus on neurology and immunology disorders – putting patients at the center of our world. Do you want to work at a world leading company that is Inspired by Patients and Driven by Science?Role Description
Are you looking for a new career opportunity within the quality assurance where you can help a company with achieving their great vision? Is ensuring the quality important to you? Do you like working in a GMP environment? Then this is the job for you? This job is for at least 6 months.Responsibilities
You will be responsible for the basic Quality Assurance tasks such as:- batch review
- Batch releases
- GMP regulations
- Validation
- CAPA
- Deviations
- SOP's
Requirements
- BSc or MSc within the Pharmacy/biotechnology or relevant to the life sciences industry- Taking initiative
- Team Player
- Hands on mentality
- At least 1 year of experiences within the QA
- Experience with a GMP / manufacturing environment
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Amber Moet.
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