Join Teva as a Senior Manager in Quality Assurance to lead compliance and quality initiatives at the Stouffville site. Drive quality culture and oversee regulatory compliance while fostering team development.
In this senior-level role, you will oversee Quality Assurance operations, ensuring adherence to SOPs, GMP, and cGMP standards. You will lead technical investigations, manage product release processes, and ensure the effectiveness of corrective actions. Your leadership will cultivate a culture of accountability and continuous improvement while working closely with production and quality teams.
Key Responsibilities:
• Lead investigations to ensure compliance with regulatory standards • Monitor and track CAPAs for effectiveness • Oversee quality system implementations and audits • Guide Quality Assurance staff through performance evaluations • Act as site QA ecosystem leader
Requirements: • Bachelor’s degree in a Science-related field • Minimum 5 years in Quality Assurance within pharmaceuticals • Solid knowledge of SOPs, GMP, and cGMP • Previous supervisory experience required • Familiar with FDA and Health Canada regulations
Utilize your expertise in quality assurance to drive excellence and compliance in pharmaceutical manufacturing at Teva. #J-18808-Ljbffr