Quality Assurance Specialist
1 month ago
Our client, a CDMO in the Montreal area, is currently looking for a Quality Assurance Specialist.
You will be involved in the development of SOPs to meet the GMP requirements of the American, European and Canadian regions.
You will have to review and approve batch records.
You will have to approve master labeling files, carry out risk assessments, make the production room clearances. You will write specifications for raw materials and packaging components, and review certificates of analysis.
We are looking for a candidate with 2-3 years' experience in quality in the pharmaceutical/biotech industry.
We have other current jobs related to this field that you can find below
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