CONSEILLIER.ÈRE AFFAIRES RÈGLEMENTAIRES ET ASSURANCE QUALITÉ/ REGULATORY AF
at Cool Simple
Saint-Laurent, QC, Canada -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 30 Apr, 2025 | Not Specified | 01 Feb, 2025 | 3 year(s) or above | Packaging,Food Industry,Management Skills,Food Studies,Food Safety,Team Spirit,Nutrition | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
REQUIREMENTS
· DEC Diploma in agri-food studies, dietetic techniques, nutrition, or other relevant training (regulatory/quality) at an equivalent level.
· Minimum of 3 years of experience in the agri-food industry.
· Bilingual in French and English – Essential.
· Knowledge of Canadian Food Inspection Agency (CFIA) laws.
· Familiarity with food safety and import regulations and standards.
· Expertise in packaging, labeling, and nutritional value regulations.
· MAPAQ certification – An asset.
· Strong knowledge of the Microsoft Office suite.
· Demonstrates organizational rigor and attention to detail.
· Excellent time and priority management skills.
· Exhibits a strong team spirit and flexibility.
How To Apply:
Incase you would like to apply to this job directly from the source, please click here
Responsibilities:
· Create product labeling for cases and individual units (UVC) and update them based on changes communicated by the CFIA (Europe/Canada transcription, ingredient declarations, nutritional value tables, barcodes).
· Participate in the development of private label packaging.
· Handle all matters related to product quality and compliance (drafting procedures, staff training for retail locations, internal controls, bacteriological standards, GMO regulations, nutritional values, etc.).
· Independently manage the importation of products from the European Union and the United States, and regularly update internal documentation and procedures (quotas, import certificates, import taxes, customs codes).
· Verify product origin rules to determine their eligibility under CETA.
· Communicate regulatory changes (food safety, HACCP, and best practices).
· Manage all documentation related to product safety (letters of guarantee, certifications).
· Perform quality tests on products according to an established schedule.
· Conduct mandatory mock product recalls and handle any actual recalls if necessary.
· Organize and participate in the annual warehouse audit and conduct audits of local suppliers.
· Manage complaints (customer, recalls, regulatory changes).
· Maintain and update databases and information in the ERP system.
REQUIREMENT SUMMARY
Min:3.0Max:8.0 year(s)
Pharmaceuticals
Purchase / Logistics / Supply Chain
Software Testing, Clinical Pharmacy
Trade Certificate
· independently manage the importation of products from the european union and the united states and regularly update internal documentation and procedures (quotas import certificates import taxes customs codes).
Proficient
1
Saint-Laurent, QC, Canada