Quality Excellence Lead (Systems, Operations and Compliance)

Position Title: Quality Excellence Lead (Systems, Operations and Compliance) Location: Brampton, Ontario (On-Site) Primary Work Location: Pickering, Ontario (On-Site) Employment Type: Full-Time Work Schedule: Monday to Friday | 9:00 AM – 5:30 PM Salary Range: $80,000 - $100,000 Work Location Flexibility: The successful candidate will initially work from the Company's Head Office in Brampton. However, the primary work location may be changed to the Company's Pickering facility or another Company location based on business requirements and operational needs. Company Description: Nanz Pharma is a globally respected Canadian healthcare company specializing in the development and manufacturing of medical devices, pharmaceuticals, and Natural Health Products (NHPs). With a strong focus on innovation, quality, and regulatory excellence, the organization is committed to delivering safe, effective, and affordable healthcare solutions that improve the quality of life for people around the world. Driven by a culture of integrity, accountability, and continuous improvement, Nanz Pharma partners with customers, healthcare professionals, and communities to develop products that meet the highest global quality and compliance standards. The company's vision is to provide trusted healthcare solutions built on quality, innovation, and excellence, while fostering an environment where talented professionals can contribute to meaningful advancements in healthcare and long-term global growth. Role Description The Quality Excellence Lead (Systems, Operations and Compliance) is a strategic and operational leadership role responsible for overseeing Quality Operations, Quality Systems (QMS), Product Release, Regulatory Compliance, and Continuous Improvement across Medical Devices, Natural Health Products (NHPs), Pharmaceuticals, and Cosmetics. Serving as the organization's quality authority, the incumbent will ensure that quality systems and operational processes remain compliant with applicable Health Canada regulations, MDSAP requirements, ISO 13485 principles, GMP, GDP, Site Licence requirements, Medical Device Licensing requirements, and other applicable domestic and international regulatory standards. As a company operating as both a manufacturer and Contract Manufacturing Organization (CMO), the role will provide quality oversight for internally developed products as well as customer-owned products manufactured under commercial agreements. The incumbent will work closely with Regulatory Affairs, Operations, Supply Chain, Manufacturing, Product Development, Procurement, Commercial teams, customers, suppliers, and third-party service providers to support regulatory approvals, product registrations, technology transfers, new product introductions, product launches, customer requirements, supplier qualification, and inspection readiness. The role requires a quality leader capable of balancing regulatory and compliance requirements with operational excellence, business continuity, customer expectations, and sustainable business growth across multiple regulated product categories and markets. Preferred Industry Experience: Demonstrated quality leadership experience within the Medical Device industry is strongly preferred . Experience within Natural Health Products (NHPs) and/or Pharmaceuticals is also highly desirable and considered a valuable asset. Key Responsibilities Lead Quality Operations, Quality Systems (QMS), Product Release, Compliance, and Continuous Improvement programs across Medical Devices, Natural Health Products (NHPs), Pharmaceuticals, and other regulated product portfolios. Serve as the designated Quality Authority for batch record review, product disposition, final product release, and quality risk-based decision-making. Provide leadership and oversight to the QA team while owning and continuously improving the Quality Management System, including CAPA, Deviations, Investigations, Change Control, Document Control, Training, Co…

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