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For one of my pharmaceutical clients in the Northern part of Brussels, I am currently looking for a Quality Engineer. The company is specialised in the production of semi-finished products for the pharmaceutical industry out of blood plasm. They have recently joined forces with multiple American and European competitors which means they are growing fast and expect a lot of challenging opportunities on short/long notice.
Role description
In this role you’ll be responsible for guaranteeing quality by following up and ensuring that all operations at all levels are done according to the applied GMP quality systems. The QA Engineers work above site which means you will be in contact with both Production and QC.
Responsibilities
Assessment of batch records, events and complaints
General QA tasks (CAPA's, change controls, deviations, risk assessments)
Participate in or supervise Improvement Projects regarding Quality
Writing of documents such as procedures, protocols and reports concerning Quality Systems
Give training to operators, engineers and technicians regarding GMP
Requirements
2+ Years of experience within the Pharmaceutical Industry (QA or QC)
Extensive knowledge of cGMP
MSc. In either (Industrial) Pharmacy or (Bio-)Chemistry preferred, Min. BSc. required
Knowledge of SAP/Trackwise is an asset
Fluent in English and Dutch or French
You are Ambitious, dedicated & hard-working
For more information please contact Seppe Verhoeven at s.verhoeven@sire-search.com or at +32 (0) 25 881 277
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