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. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together. We are seeking a highly experienced Senior Manager, Quality Assurance to lead Quality Assurance operations at our Stouffville manufacturing site.

This role is responsible for providing leadership, technical expertise, and strategic direction to ensure all Quality Assurance activities are conducted in compliance with SOPs, GMP, and cGMP requirements. The successful candidate will oversee quality systems, product investigations, product release activities, regulatory compliance, and team development while driving a culture of quality, accountability, and continuous improvement. Lead and oversee investigations related to products manufactured at the site, ensuring compliance with regulatory requirements and company standards.

Oversee the management and investigation of customer, healthcare professional, and regulatory product complaints. Provide expert guidance on quality procedures, SOPs, GMP, and cGMP requirements to Production and Quality teams. Maintain current knowledge of FDA and Health Canada regulations governing pharmaceutical manufacturing, packaging, testing, distribution, and quality systems.

Oversee manufacturing batch record reviews, product release activities, document issuance, and document control processes. Act as the Site QA Ecosystem Lead, ensuring the successful implementation and maintenance of quality systems and learning management infrastructure. Manage retained sample programs for raw materials and finished products in accordance with regulatory requirements.





Oversee returned goods processes and ensure only acceptable product is returned to inventory. Lead, coach, mentor, and develop Quality Assurance staff through performance management, career development, and succession planning initiatives. Participate in and support regulatory inspections and internal audits.

Promote Environmental

Health & Safety (EHS) programs, including hazard identification, incident investigations, root cause analysis, and corrective action implementation. Foster a culture of continuous improvement, quality excellence, and regulatory compliance. Bachelor's degree in a Science-related discipline required. Minimum of 5 years of relevant experience in Quality Assurance within a pharmaceutical, biotechnology, or related regulated manufacturing environment.

Experience managing quality systems, investigations, audits, and regulatory compliance activities.

Experience with TrackWise, Oracle, LIMS, Smart QA, and Microsoft Office applications. Understanding of pharmaceutical manufacturing operations, HVAC systems, purified water systems, and statistical analysis. Strong leadership, coaching, and team development skills. Proven planning, prioritization, and organizational abilities. Ability to manage multiple priorities in a fast-paced environment. Strong attention to detail and commitment to quality and compliance. Travel as required.

At Teva





Canada we provide a rewarding and collaborative work experience, with growth opportunities and development opportunities for employees, in a safe and caring environment! The base pay offered may vary depending on job-related knowledge, skills, experience, education, and internal equity. In addition to base salary, this role may qualify for an annual bonus based on employment type.

Teva Canada’s choices Benefit Plan including Health, Dental, Disability, Life Insurance Employee Assistance Program & Virtual Health Programs Retirement Savings Programs Time for yourself or those you care about, through paid time for Vacation, Wellness days, Care/Sick days, Teva Days and Volunteer Days More exciting details on the specific total rewards offerings to be provided at the offer stage depending on the position and employment type hiring for. This position will fill a current vacancy and Teva Canada may use an artificial intelligence (AI) system to assist with the initial screening and evaluation of job applications by analyzing for relevant skills, professional experience, and education, that best match the posted job qualifications. Teva Pharmaceuticals is committed to equal opportunity in employment.

It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. EOE including disability/veteran #

📌 Senior Manager, Medical Writing (Whitchurch-Stouffville)
🏢 Teva Pharmaceuticals
📍 Whitchurch-Stouffville