Who are we?

Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas.  We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth!

Position Summary

The position maintains and ensures data accuracy within various applications for QC data.  The position also analyzes data and reports to provide the business with information to make tactical and strategic decisions. Under the direction of the Quality Control Manager, this position is responsible for performing the necessary tasks to ensure compliant and successful enhancement of projects in Quality Operations.

Responsibilities: 

• Coordinate, monitor, and perform activities related to department projects 

• Chairing project meetings, recording minutes, discussing issues and recommending solutions, tracking tasks and actions, and implementing project initiatives to achieve departmental objectives
• Participate in process, cycle time, and/or other improvement projects in QC
• Perform project timelines and budget analysis, and monitor project status and metrics through to completion.  Proactively consider alternative contingencies and take steps to ensure project goals and timelines are met
• Coordinate and liaise with personnel from other departments and divisions within Teva Canada, and other Teva business units to meet overall project timelines and achieve the objectives and organizational goals
• Coordinate departmental contributions and serve as a contact person for joint/shared projects involving local and/or global sites
• Generate and gather project data and documentation (e.g. Project status reports, cost/benefit analysis, Gantt charts), ensuring data is accurate, validated, and meaningful
• Identify opportunities for process improvements, cost savings, and efficiency/productivity goals
• Support vendor management QTA review process

Required Skills:

• Bachelor of Applied Science in Industrial Engineering or related science discipline
• Project Management Professional (PMP) designation, or in the process of obtaining this designation
• Project management experience, with specific experience managing concurrent pharmaceutical projects preferred

Function

Sub Function

Reports To

In process of validation

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