GMP compliance and exact records define this fully onsite Processing Operator I role with Kenvue in Guelph, Ontario, supporting bulk pharmaceutical production.
Under minimal direction, the Processing Operator I processes raw materials and documents activities according to validated processes and SOPs. You will help maintain quality, safety, and compliance while working across core manufacturing functions. Kenvue seeks Grade 12 education, mechanical aptitude, and proficiency in Microsoft Word, Excel, and SAP. Post-secondary chemistry, biology, or biochemistry education is desired, as is regulated food or pharmaceutical manufacturing experience.
Key Responsibilities: Process raw materials under validated procedures
Follow GMPs and GDPs throughout manufacturing activities
Identify potential quality concerns and report deviations
Identify safety issues and complete required training
Keep training records updated within required timelines
Requirements: Grade 12 education
Mechanical aptitude
Understanding of GMP compliance
Proficiency in Microsoft Word, Excel, and SAP
Two to three years regulated manufacturing experience preferred
Support Kenvue’s regulated pharmaceutical manufacturing with GMP discipline, mechanical aptitude, SAP proficiency, and accurate documentation.