QA Lead: GDP
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Air Liquide Belgium is seeking a Quality Assurance Lead to maintain the Quality Management System in line with GDP and ISO 13485 / MDR for medical devices and medicines. You will lead document management, CAPA, audits, changes, and supplier qualifications within the Benelux context.
You will ensure training, QA awareness, and oversee storage conditions, FEFO expiry management, and pest control at Zemst, collaborating with the Benelux Quality & Safety Manager to harmonize processes.
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Quality Assurance Lead
Il y a 6 heures
Zemst, Flanders, Belgique airliquidehr Temps pleinh3How will you CONTRIBUTE and GROW? /h3pAs Quality Assurance Lead, you are part of the Benelux Pharmaceutical / Quality Department and you report to the Quality Safety Manager Benelux. /ppYou are responsible to maintain the Quality Management System according to the Good Distribution Practices (GDP - medicines) and ISO 13485 / MDR (Medical Devices as a...
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QA Lead: GDP
Il y a 6 heures
Zemst, Flanders, Belgique airliquidehr Temps pleinpAir Liquide Belgium is seeking a Quality Assurance Lead to maintain the Quality Management System in line with GDP and ISO 13485 / MDR for medical devices and medicines. You will lead document management, CAPA, audits, changes, and supplier qualifications within the Benelux context. /ppYou will ensure training, QA awareness, and oversee storage conditions,...
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Quality Assurance Lead
Il y a 22 heures
Zemst, Belgique Air Liquide Temps pleinHow will you CONTRIBUTE and GROW?As Quality Assurance Lead, you are part of the Benelux Pharmaceutical / Quality Department and you report to the Quality & Safety Manager Benelux. You are responsible to maintain the Quality Management System according to the Good Distribution Practices (GDP - medicines) and ISO 13485 / MDR (Medical Devices as a distributor)...
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Quality Assurance Lead
Il y a 2 heures
Zemst, Flanders, Belgique airliquidehr Temps pleinHow will you CONTRIBUTE and GROW? As Quality Assurance Lead, you are part of the Benelux Pharmaceutical / Quality Department and you report to the Quality & Safety Manager Benelux. You are responsible to maintain the Quality Management System according to the Good Distribution Practices (GDP - medicines) and ISO 13485 / MDR (Medical Devices as a distributor)...