In a GMP and HACCP regulated environment
- Verify calculations, raw data, transcripts and analysis results;
- Verify various records of laboratory instruments;
- Check manufacturing and packaging sheets;
- Writing and authorizing quality documents;
- Reconciliation of controlled material;
- Verify analytical methods;
- Other documentary tasks.
Profile searched:
- Specialized training in Quality Assurance or B.Sc. in chemistry, biochemistry, microbiology or engineering;
- 0-2 years experience in a GMP and GLP environment;
- 0-2 years experience in quality assurance;
- Bilingual, spoken and written (English/French);
- Thorough and analytical;
- Able to manage time and priorities well;
- Good interpersonal relationships.
Organization
Lallemand is a privately held Canadian company founded in the late 19th century, which develops, produces, and markets microorganisms for various markets. The administrative offices of the parent company are in Montreal, Canada. Today, Lallemand employs more than 5,000 people working in more than 45 countries on 5 continents.
Please take note that accommodations will be provided in all parts of the hiring process. Applicants need to make their needs known in advance.