We Are TevaWe're Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it's innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we're dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.

We Are TevaWe're Teva, a leading cutting-edge biopharmaceutical company, enabled by a world-class generics business. Whether it's innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we're dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.

Our Team, Your Impact

Production Supervisor (Day, Afternoon, and Night Shifts Available)

Stouffville, Ontario

We're looking for an experienced and people-focused Production Supervisor to lead manufacturing and packaging operations in a highly regulated environment. In this role, you will oversee daily production activities, ensure compliance with GMP and Health & Safety standards, drive operational excellence initiatives, and develop high-performing teams. You will play a critical role in ensuring products are manufactured safely, efficiently, and in accordance with quality requirements.

How You'll Spend Your Day





Production Leadership

- Lead and direct production staff to successfully execute manufacturing and packaging schedules.
- Translate business priorities and production plans into daily team objectives and assignments.
- Monitor production activities and address operational issues in real time to ensure targets are achieved.
- Review, complete, and release production documentation and maintain accurate records within ERP systems.

Quality & Compliance

- Ensure all activities are performed in accordance with GMP requirements, approved procedures, and production records.
- Review and complete production documentation while maintaining data integrity standards.
- Investigate deviations, non-conformances, and quality events; implement corrective and preventive actions (CAPAs).
- Ensure all employees remain current with required training and compliance requirements.

People Leadership

- Foster a positive, collaborative, and high-performing team culture.
- Coach, mentor, and develop employees through ongoing feedback and performance management.
- Conduct performance reviews and support individual development planning.
- Manage employee attendance, performance concerns, and disciplinary matters in partnership with Human Resources when required.




- Facilitate regular communication meetings to ensure alignment with departmental objectives.

Safety & Environmental Responsibility

- Champion a strong safety culture and ensure compliance with OHSA, WHMIS, PPE, and company EHS requirements.
- Conduct regular floor walks to identify and address safety concerns.
- Lead incident investigations, root cause analyses, and corrective actions.
- Act as the site's responsible leader during off-shifts when required.

Continuous Improvement

- Identify opportunities to improve productivity, quality, and operational efficiency.
- Lead and support Lean and Operational Excellence initiatives, including Kaizen, SMED, OEE, 5S, and employee idea generation programs.
- Collaborate cross-functionally with Quality, Engineering, Technical Services, Maintenance, and other departments to solve operational challenges.

Your Skills And Experience

Education

- Bachelor's degree in Science, Pharmacy, Engineering, or a related discipline.
- Equivalent education and experience may be considered.

Experience

- 3+ years of experience in a Production, Manufacturing, Quality Assurance, or related GMP-regulated environment.
- Previous supervisory or team leadership experience preferred.
- Experience within pharmaceutical, food manufacturing, or another regulated industry is highly desirable.

Technical Skills

- Strong understanding of GMP requirements and regulated manufacturing environments.
- Experience with ERP systems and Microsoft Office applications.
- Familiarity with deviation management systems, computerized maintenance systems, safety management systems, and time and attendance platforms.
- Knowledge o

📌 Production Supervisor (Whitchurch-Stouffville)
🏢 Teva Pharmaceuticals
📍 Whitchurch-Stouffville