Quality Assurance Manager
đ
Quality Assurance Manager, Global Compliance
đ
Stayner, ON (Onâsite)
đ
18â20 Month Contract
đ” $87,000â$93,000 + Benefits & Vacation Entitlement
âïž
Occasional Travel Within Canada
Weâre looking for a motivated and collaborative Quality Assurance Manager, Global Compliance to oversee our Quality Management System (QMS) and ensure full compliance with Health Canada Regulations, U.S. FDA GMP, and other regulatory standards.
In this role, youâll play a critical part in supporting new product launches and ongoing commercial operations across Canada and the U.S. Youâll lead audits, manage investigations, resolve customer/supplier concerns, and provide the quality leadership that keeps our operations strong and compliant.
If you thrive in a dynamic environment, enjoy building efficient systems, and love leading with your teamânot just directing themâthis opportunity is for you.
What Youâll Be Accountable ForAs the Quality Assurance Manager, you will own the Quality Management System and ensure the QA department operates effectively and compliantly. Youâll use your leadership, decisionâmaking skills, and technical knowledge to maintain product quality, regulatory alignment, and operational excellence across both Canadian and U.S. markets.
Key Responsibilities Compliance & Quality Systems (QMS / eQMS / Documentation / Training)- Ensure compliance with SOPs and regulatory requirements (Health Canada, FDA).
- Oversee global records management and administration of the Trackwise eQMS.
- Approve SOPs, product specifications, and controlled documents.
- Deliver QMS and compliance training to internal teams.
- Support development and continuous improvement of quality processes and procedures.
- Maintain Quality Assurance Person (QAP) or Alternate QAP designation with Health Canada, as required.
- Conduct investigations for complaints, deviations, and material review issues.
- Resolve customer and supplier quality concerns with professionalism and urgency.
- Lead crossâfunctional teams to complete deviations, CAPAs, and change controls.
- Approve all stages of quality documentation (complaints, SCARs, CAPAs, deviations, audit findings).
- Analyze quality metrics to identify trends and implement corrective/preventive action.
- Lead regulatory inspections and customer audits.
- Manage the internal and external audit program, ensuring timely CAPA closure.
- Facilitate product recalls and support returns as required.
- Build strong relationships with customer QA teams to address quality issues proactively.
- Support daily QA operations, qualifications, validations, and engineering protocols.
- Demonstrated business planning and execution abilities.
- Collaborative and supported leadership (4 direct reports).
- Work closely with suppliers and CMOs to ensure quality expectations are met.
- Collaborate with the Quality team and senior leadership on priorities and improvements.
- Promote a culture of efficiency, teamwork, and shared success.
- Contribute to business planning and execution.
- Perform other duties as assigned.
- Occasional travel within Canada
- Required participation in meetings and presentations
- Overtime as operationally required
- 3â5 years of experience in a Health Canada or FDAâregulated industry (Food, Pharma, Cosmetic, Cannabis or similar)
- Postâsecondary education in a related field; B.Sc. preferred
- Strong experience interacting with regulatory agencies
- Knowledge of Health Canada Regulations, FDA GMP, and EU GMP
- Proficiency with Microsoft Word, Excel, Access, SharePoint, and Visio
- Experience with Trackwise eQMS and SAP is a strong asset
- Excellent problemâsolving, project management, and communication skills
- A highly collaborative, teamâfocused leadership style
đ Via Link In or
Questions? Call 705â408â0313#J-18808-LjbffrTo Search, View & Apply for jobs on this site that accept applications from your location or country, tap here to make a Search: