Project Manager, Manufacturing Investigations

2 days ago


Richmond Hill, Ontario, Canada Apotex Full time

About Apotex Inc.

Apotex Inc. is a global health company that produces high-quality, affordable medicines for patients worldwide. With a presence in over 75 countries, Apotex employs almost 7,200 people in manufacturing, R&D, and commercial operations.

Job Summary

The Project Leader, Production Investigations, is responsible for ensuring all investigations within the Manufacturing and Production departments at the Richmond Hill site are completed efficiently and in a timely manner. This involves ensuring established procedures are followed and corrective and preventative actions are implemented.

Key Responsibilities

  • Investigate manufacturing deviations and document findings in compliance with site procedures and GMPs.
  • Identify critical paths for investigations to ensure timely root cause analysis and implementation of corrective and preventative actions.
  • Facilitate meetings with Subject Matter Experts (SMEs) as required.
  • Perform thorough impact analysis in collaboration with SMEs, including vendors.
  • Ensure accurate identification of root cause, corrective action, and preventative action for all completed investigations.
  • Regularly review progress on open investigations with the Production Investigations team, QA approver team, and Production Management team to ensure timelines are attainable.
  • Evaluate and escalate any roadblocks or issues that may impact investigation timelines.
  • Prepare clear, concise investigation reports and review them for completeness and accuracy prior to approval by the Department Manager.
  • Lead cross-functional projects associated with manufacturing deviation reduction initiatives.
  • Support Production Supervisors/Team Leaders in initiating investigations and gathering relevant information in a timely manner.
  • Operate in accordance with Apotex's Code of Conduct and Business Ethics, as well as established regulatory, compliance, and safety requirements.
  • Perform all work in support of Apotex's Values: Collaboration, Courage, Perseverance, and Passion.
  • Work in a safe manner and collaborate as a team member to achieve all outcomes.
  • Ensure personal adherence to all compliance programs, including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies.

Requirements

  • Post-secondary degree in Engineering, Sciences, or a related technical field preferred or equivalent combination of College diploma and experience in a manufacturing environment.
  • Fluency in project management and Root Cause Corrective Action (RCCA) tools.
  • Superior organizational, interpersonal communication skills.
  • Ability to manage time effectively and work independently in a fast-paced environment.
  • Strong command of the English language, both written and verbal.
  • Knowledge of Good Manufacturing Practices (GMPs).
  • Proficiency with Microsoft Word, Excel, and SAP.
  • 5-7 years' experience in a pharmaceutical or manufacturing industry, preferably in a Manufacturing, Engineering, or QA/QC role.

At Apotex, we are committed to fostering an inclusive, accessible work environment where all employees feel valued, respected, and supported.

Apotex offers accommodation for applicants with disabilities as part of its recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require an accommodation.



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