Review of batch records and monitoring of master document;
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;
All other functions related to GMP compliance.
Periodic literature review;
Receipt and evaluation of the adverse events reports, writing of the CIOMS;
Follow-up on the received adverse events;
Review and preparation of the annual pharmacovigilance reports.
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);
Ability to work under minimal supervision (possibility of tele-working);
Ability to monitor multiple priorities and strong organizational skills;
Excellent written and verbal communications.
Please fill out the form to apply
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Application from outside Canada
Finding an employer that will assist you in your work permit without knowing you is utopic.. Employers simply do not consider non-resident applications. We strongly recommend that you immigrate to Canada before you start looking for employment.