Revision of batch records.
Monitoring of master documents.
Writing and monitoring of SOP.
Writing and revision of validation and stability protocols.
Monitoring of quality complaints, deviations, CAPA and change control systems.
Monitoring of retains and stability samples.
Evaluation of returns.
All other functions related to GMP compliance.
Bachelor degree in Science or in a related field.
Perfect knowledge of GMP.
Minimum of 5 years' experience in the pharmaceutical industry.
Perfectly bilingual (English & French).
Strong ability for solving complicated situation.
Ability to work under minimal supervision.
Ability to monitor multiple priorities and strong organizational skills.
Good knowledge of Microsoft Office (Word, Excel, PowerPoint, Access, etc.)
Excellent in written and verbal communications.