Job Description

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Manufacturing Clerk
Job Location: Laval, Quebec, CAN
Job Requisition ID: 14469
Join our global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes to our patients. We are all in it together to make a difference. Be a part of a culture that doesn't just wait for change but actively creates it-where your skills and values drive our collective progress and impact.
What a manufacturing Clerk does at Bausch:
As a member of the production team, you will be crucial in the maintaining production efficiency and product quality. In this position, you will adhere to production guidelines, accurately documenting processes, and monitoring product quality. The role will be proactive reporting of issues and proposing improvements, ensures operational excellence and safety protocols are upheld throughout production processes.
(Contract - 24 months)

• Perform filling, operating, and packaging tasks for the Arestin Unit following established procedures.
• Ensure adherence to production steps specified in production sheets.
• Complete production documentation accurately and promptly; monitor and control product quality, reporting process deviations to management as necessary.
• Conduct product inspections as needed and maintain equipment availability.
• Maintain workstation and equipment in accordance with Good Manufacturing Practice (GMP) and Health, Safety and Environmental (HSE) standards.
• Participate in teamwork, contribute to developing new methods, and maintain technical qualifications.
• Fulfill additional tasks as assigned by the manager.
• Verify equipment, materials, and premises for functionality and compliance, use equipment properly.
• Inform team leader/manager of encountered issues, adhering to production standards.
• Assemble equipment, wash premises, and complete batch files and packaging documents.
• Take necessary measures to ensure safety and integrity during anomalies.
• Record entries in production management systems.
• Work in compliance with GMP and HSE standards, applying directives daily.
• Promptly report quality or HSE concerns to management and propose improvements.

Minimum Requirements:

• Secondary minimum V or equivalent, DEP or DEC
• 3 years of experience in a pharmaceutical industry or related field as an employee or operator
• Technical knowledge of processes/products Knowledge of production tools.

We are an Equal Opportunity Employer. EOE Disability/Veteran. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates collaboration.

Skills Required