The candidate will be responsible for performing microbiological analyses related to all stages of the manufacture of pharmaceutical products and/or sterile medical devices, in accordance with existing regulations such as GMP, ISO, USP, etc. He or she may be required to perform basic chemical analyses.
Perform microbiological tests (biological loads, endotoxin analysis, sterility, etc.), environmental sampling, culture medium qualification tests, and bacterial strain testing in accordance with various international pharmacopoeias, ISO (medical devices), etc.
Contribute to all quality control processes, from raw materials to finished products.
Ensure compliance and delivery of documents associated with analyses.
Comply with the schedule and deadlines in accordance with manufacturing.
May be required to perform physical tests
Minimum college diploma in a discipline related to biochemistry, biology, or microbiology.
Experience in quality control, preferably in the pharmaceutical industry, would be an asset.
Knowledge of computer software (Word, Excel).
Ability to work effectively within a team
Knowledge of chemistry would be an asset.
Bilingual (French/English) in both spoken and written communication.
Day shift, 40 hours per week
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