Director of Production

Location: Mirabel, Quebec

ABOUT THE COMPANY

Our client is an innovative pharmaceutical company specializing in the development and manufacturing of cannabis-based products. Operating within a highly regulated GMP environment, the company is committed to delivering safe, consistent, and high-quality medicinal cannabis products through a culture of quality, innovation, and continuous improvement.

As the organization continues to grow, the are investing in its people, technology, and operational capabilities to strengthen its position as a trusted manufacturing partner within the Canadian cannabis industry.

SUMMARY:

As our client continues to expand its manufacturing capabilities, they are seeking an experienced Director of Production to lead and optimize all production operations within their GMP-regulated facility.

This is a key leadership role responsible for overseeing production planning, manufacturing execution, quality compliance, and continuous improvement initiatives while ensuring products are manufactured safely, efficiently, and in accordance with Good Manufacturing Practices (GMP). The successful candidate will lead a high-performing production team, collaborate cross-functionally with Quality Assurance, Supply Chain, R&D, and Compliance, and play a critical role in supporting the company's continued growth and operational excellence.

RESPONSIBILITIES:

• Lead all production activities including production planning, scheduling, batch execution, and on-time delivery of manufacturing targets.
• Develop and execute the site's manufacturing strategy to support business growth, operational scalability, and long-term production objectives.
• Partner with the Executive Leadership Team to establish annual operational goals, capital investment priorities, and manufacturing performance targets.
• Ensure compliance with Good Manufacturing Practices (GMP), regulatory requirements, and our client's own quality standards.
• Review, approve, and maintain batch manufacturing records to ensure accuracy, traceability, and regulatory compliance.
• Forecast raw material and consumable requirements based on production plans and commercial forecasts while coordinating procurement using a Just-in-Time inventory approach.
• Ensure all manufacturing activities comply with quality, safety, and regulatory standards.
• Recruit, mentor, coach, and evaluate production supervisors and manufacturing personnel while fostering a culture focused on quality, compliance, teamwork, and continuous improvement.
• Monitor operational performance against production schedules, budgets, and established KPIs.
• Ensure accurate, real-time production and inventory transactions within the ERP system.
• Maintain eligibility for the required security clearance to access secured production areas.
• Promote a strong health and safety culture by ensuring compliance with workplace safety standards and proper use of personal protective equipment (PPE).
• Identify and implement continuous improvement initiatives to enhance manufacturing efficiency, productivity, and profitability.
• Lead manufacturing process and equipment validation activities in collaboration with the Compliance and Quality teams, including validation protocol execution and documentation.
• Develop, review, and maintain Standard Operating Procedures (SOPs) to ensure manufacturing practices accurately reflect production floor activities.
• Partner closely with Quality Assurance during internal audits, regulatory inspections, and compliance activities.
• Lead investigations into production deviations and participate in the development and implementation of Corrective and Preventive Actions (CAPAs).
• Support ongoing employee training and professional development while helping build internal training capabilities.
• Collaborate with the R&D team to support new product development, process transfers, and manufacturing innovation initiatives.

EDUCATION & EXPERIENCE:

• Bachelor’s degree in engineering, Science, Pharmacy, or a related discipline.
• Master’s degree in Pharmacy, Chemistry, Biotechnology, or a related field considered an asset.
• Minimum 5 years of leadership experience managing manufacturing or packaging operations within pharmaceutical, biotechnology, food, or other GMP-regulated industries.
• Demonstrated experience leading manufacturing teams in highly regulated production environments.
• Strong understanding of Good Manufacturing Practices (GMP), manufacturing validation, and regulatory compliance.
• Proven leadership, communication, planning, and problem-solving skills.
• Strong organizational and project management skills with the ability to manage multiple priorities in a fast-paced environment.
• Excellent analytical skills with the ability to make informed, data-driven decisions.
• High degree of integrity, accountability, and attention to detail.
• Advanced proficiency with Microsoft Office and ERP systems.
• Valid driver's licence.
• Fluent in French with professional working proficiency in English preferred.

White Ash Group and the companies it represents are Equal Employment Opportunity employers that values the strength of diversity within the workplace. All qualified applicants, regardless of race, colour, religion, gender, sexual orientation, marital status, gender identity or expression, nationality, age, disability or veteran status, or any other characteristic protected by applicable law, are strongly encouraged to apply.