Sr. QA Officer - Limburg
Location: NetherlandsSIRE® 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 organisation, based in Netherlands.
Monitor compliance with all applicable GMP and safety standards
Support the Qualified Person in his role
Write, review and approve documentation
Handle, distribute and archive controlled documents.
Support and attend internal and external audits.
Suggest process improvements and actively follow up improvement projects
Involved in planning activities
Provide guidance to QA Officers.
Suggesting training activities.
At least 3,but preferably 5 years of experience in a similar role
Sound knowledge of GMP and compliance
Fluent in English
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Seppe Verhoeven.
The Company
.Role Description
The Senior QA Officer is responsible for planning and execution of daily quality assurance activities while ensuring compliance with international quality requirementsResponsibilities
Plan and execute quality assurance activitiesMonitor compliance with all applicable GMP and safety standards
Support the Qualified Person in his role
Write, review and approve documentation
Handle, distribute and archive controlled documents.
Support and attend internal and external audits.
Suggest process improvements and actively follow up improvement projects
Involved in planning activities
Provide guidance to QA Officers.
Suggesting training activities.
Requirements
A master in chemisty/biochemistryAt least 3,but preferably 5 years of experience in a similar role
Sound knowledge of GMP and compliance
Fluent in English
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Seppe Verhoeven.
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