Quality Assurance Assistant

Updated: April 10, 2024 10:29 PM GMT

NOVADIP Biosciences S.A.

Mont-Saint-Guibert

Your responsibilities
• Supervise the strict application of cGMP, GCP and GLP regulations during each step of the production and analysis of batches of experimental medicinal products
• Assist with the management (check, approval, distribution) of specifications, work instructions and other Novadip quality system documents
• In collaboration with QC and the QP, assist with the management of the storage facilities for raw materials, intermediates, finished products and packaging materials
• Manage the release of Novadip materials in close collaboration with the Logistics department
• Manage suppliers
• Revise batch records from production and quality control data
• Monitor archiving and traceability of all quality system documents, with the assistance of the administrative staff when necessary
• Assist with the supervision of storage conditions of products, materials and consumables
• Assist with the checking and approving of certificates of analysis
• Assist with the monitoring of... More Detail