Job opportunity
Microbiology Quality Control Technician
Werfen
Use microbiological procedures and sterile culturing skills as Werfen’s Laboratory Technician I in Quality Control, working Canada’s first shift. Support compliant diagnostic production.
Werfen seeks a Laboratory Technician I to perform microbiology and product testing within Quality Control. This position handles environmental, personnel, and product sampling while supporting validation, receiving inspection, and final product evaluation. Responsibilities also include maintaining records, inventories, equipment, and retention samples. The role requires understanding cGMP, Health Canada requirements, biosafety hazards, and manufacturing processes for in vitro diagnostic devices.
Key Responsibilities:
Perform sterile bulk, pre-vialing, and post-vialing culturing
Complete environmental, personnel, and product sampling within defined timeframes
Conduct validation, verification, and acceptance testing activities
Quarantine, isolate, or destroy nonconforming materials and products
Assist with product complaint investigations and technical inquiries
Requirements:
Bachelor’s degree in Biological Sciences or related discipline
At least six months of quality control experience
Understanding of cGMP and Health Canada requirements
Knowledge of WHMIS and biohazardous disposal procedures
Proactive problem-solving and strong organizational skills
Apply microbiology, sterile technique, validation, and compliance knowledge to support Werfen’s quality control laboratory operations.
#J-18808-Ljbffr
Apply on source site Werfen seeks a Laboratory Technician I to perform microbiology and product testing within Quality Control. This position handles environmental, personnel, and product sampling while supporting validation, receiving inspection, and final product evaluation. Responsibilities also include maintaining records, inventories, equipment, and retention samples. The role requires understanding cGMP, Health Canada requirements, biosafety hazards, and manufacturing processes for in vitro diagnostic devices.
Key Responsibilities:
Perform sterile bulk, pre-vialing, and post-vialing culturing
Complete environmental, personnel, and product sampling within defined timeframes
Conduct validation, verification, and acceptance testing activities
Quarantine, isolate, or destroy nonconforming materials and products
Assist with product complaint investigations and technical inquiries
Requirements:
Bachelor’s degree in Biological Sciences or related discipline
At least six months of quality control experience
Understanding of cGMP and Health Canada requirements
Knowledge of WHMIS and biohazardous disposal procedures
Proactive problem-solving and strong organizational skills
Apply microbiology, sterile technique, validation, and compliance knowledge to support Werfen’s quality control laboratory operations.
#J-18808-Ljbffr