Director of Operations

4 weeks ago


WhitchurchStouffville, Canada Tevapharm Full time
p>Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. p>The opportunity

The Director Operations Canada is responsible for the Production activities at three Canadian Sites (Stouffville, 30N & Hood Road). The position is responsible for the timely production of solid dose products in a manner which meets market demand, GMP and Regulatory requirements, business plans and Safety requirements. Also provides site staff with a working environment of open communication, mutual trust and respect, empowering employees in Continuous Improvement (OpEx) through training and experience consistent with the requirements of customer demand, in a compliant manner.

How you’ll spend your day

Leadership:

Manage the effective recruitment, deployment and utilization of staff while controlling labour hours and variable cost to meet production targets.
Provide effective leadership to Manager and Supervisory staff, ensuring fair and equitable treatment of employees by enforcing consistent application of Human Resources Policies/Procedures and company culture.
Lead, develop and manage strategic activities toward achieving Annual Work Plan / LE.
Lead the development of Production objectives and ensure the plant activities are aligned to deliver results.
Participate in sites events (i.e. p>

Quality Compliance:
Lead production SOP, GMP, and SOX compliance.
Act on behalf of the company during Regulatory Inspections and communications with Health Canada, FDA and Global Quality operations and 3rd party customers.
Support the development and implementation of CAPAs while ensuring compliance with all regulatory and corporate quality standards./>Identify and implement continuous improvement opportunities to optimize site efficiencies, capacity and quality compliance.
Support corporate continuous improvement projects.
Partner with Engineering in the identification and implementation of facility and/or equipment requirements in support of CI initiatives.
Manage the Solid Dose site hopper plan (focusing on creating and implementing cost savings).

Productivity:
Actively participate in developing strategic site planning models to increase volume capabilities.
Oversee the execution of the Production Schedule.

5+ years of experience in a manufacturing environment at a management/supervisory level.

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