Manufacturing Operator

• In compliance with established policies, directives, procedures, manufacturing instructions, and in accordance with Good Manufacturing Practices (GMP), as well as health, safety, and environmental protection measures and business processes at the Montreal site, the main responsibilities of the manufacturing operator are:
• As a member of the process-centered team, the manufacturing operator is responsible for producing various dosage forms and performing different process steps such as weighing, granulation, blending, compression, encapsulation, coating, and inspection of solid, semi-solid, or liquid dosage forms according to their professional specialty, while meeting criteria across the following dimensions: Safety, Quality, Delivery, Cost, and People.
• They are also responsible for cleaning and maintaining equipment and tools in their area, as well as their workspace.
• They must perform the production steps under their responsibility, carry out required inspections and controls, and document their actions according to manufacturing instructions and standard work procedures.

• All the following tasks are performed in compliance with policies, directives, procedures, manufacturing instructions, GMP, health, safety, and environmental protection measures, and Montreal site business processes.

• Disassembly, cleaning, and assembly of production equipment according to procedures and GMP
• Planning cleaning activities to optimize production schedules and use of cleaning rooms
• Checking the cleanliness and condition of parts and/or equipment
• Starting certain production equipment
• Performing room or section clearance activities
• Evaluating equipment and product quality
• Proper documentation (manufacturing records, logs, cleaning labels, standard work charts, etc.) according to GMP
• Printing and/or inspection of tablets or capsules according to standards
• Performing preventive maintenance (TPM)
• Polishing punches
• Waste management (trash and/or pharmaceutical waste)
• Storage of parts
• Following up on requests with specialists or supervisors
• Handling certain equipment and products (powders, cores, tablets)
• Verifying raw materials
• Performing sanitation tasks
• Performing certain reconciliations
• Maintaining proper inventory of products/materials/supplies
• Occasional replacement of Level 2 operators
• Identifying problems and proposing solutions
• Participating in T0 T1 meetings and continuous improvement loops
• Training colleagues
• Actively participating in continuous improvement programs and submitting ideas via the t-card system
• Participating in team committees if required (e.G., HSE, operational excellence, CCM, special projects, job evaluation, etc.)
• Performing training follow-up tasks if required (updating training curricula, modules, procedures, etc.)

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