Cosmetics manufacturing facility, Mississauga. Contract until June 30, 2027, with possible extension. 12-hour day shifts, Friday to Monday, 7:30 AM–7:30 PM. Immediate start.
Responsibilities
Review executed batch sheets and Master Batch Packaging Records (MBPRs) to meet finished goods release schedules
Review third-party manufacturer release documentation and Certificates of Analysis (CofA) for QC and microbiology testing, and release finished goods to market
Prepare Certificates of Conformance (CofC)
Review and approve Bills of Materials (BOMs)
Create, review, and approve Packaging Assembly Instructions (PAI)
Collect and compile all bulk and finished goods release documentation before release
Evaluate batch release and retention samples
Release finished products in the ERP system and send release documentation to the relevant departments
Issue, review, and archive batch records and release documentation to support sample and material disposition
Track release documentation in spreadsheets,
and prepare boxes for storage of documentation and retain samples
Support product rework, localization, and related documentation
Support regulatory audits and archive quality documents per SOPs and cGMP
Identify, report, and resolve GMP gaps
Contribute to quality continuous improvement projects
Work extended hours when release deadlines require
Qualifications
Post-secondary diploma or degree in a science or Quality Assurance field (Bachelor of Science preferred)
1+ year in the pharmaceutical, food, or cosmetic industry, preferably in QA
Familiarity with GMP
Experience with Microsoft Word and Excel
Pay: $18.65 per hour
Expected hours: 48.0 per week
Perks:
In office parking
Education:
DCS / DEC (preferred)
Experience:
Quality assurance: 1 year (required)
GMP: 1 year (required)