We’re Hiring: QA/QC Supervisor
Wandler Probiotics Inc. is a young, vibrant, and growing company where collaboration, initiative, and continuous improvement are at the heart of what we do. We’re looking for a detail-oriented and proactive QA/QC Supervisor to join our team, oversee our quality systems, ensure regulatory compliance, and maintain high standards across our manufacturing operations. This is an opportunity to make a meaningful impact, bring fresh ideas, and grow with us as we continue to evolve.
Key Responsibilities
- Establish, maintain, and continuously improve the Quality Management System (QMS) in compliance with current Good Manufacturing Practices (cGMP).
- Conduct quality audits, monitor system performance, identify trends, and drive continuous improvement.
- Develop, review, and maintain SOPs, specifications, protocols, test methods, and other quality documentation.
- Oversee manufacturing in-process controls to ensure products consistently meet quality requirements.
- Qualify and monitor third-party service providers, including contract manufacturers and laboratories.
- Review and approve or reject quality documents, changes, reprocessing and rework procedures, and production batch records.
- Make final decisions on product lot release in accordance with applicable requirements.
- Lead investigations of non-conformances, discrepancies, and quality failures, ensuring root causes are identified and corrective and preventive actions (CAPAs) are implemented.
- Support regulatory inspections, manage inspection responses, and ensure issues are resolved and documented.
- Communicate quality risks, regulatory updates, and system performance to management.
- Maintain clear documentation of roles and responsibilities while ensuring independent and objective quality oversight.
- Support employee training and stay current with evolving regulatory requirements and industry best practices.
Qualifications & Skills
- Bachelor’s degree (B.Sc.) in a relevant field.
- 2–5 years of experience in a similar role or regulated industry, such as food, natural health products (NHPs), pharmaceuticals, cosmetics, biotechnology, or ISO-regulated manufacturing is an asset but not required.
- Knowledge of GMP guidelines and applicable regulations, including U.S. FDA 21 CFR Part 111 and ANSI-455-2.
- Supervisory experience is an asset.
- Strong leadership, interpersonal, and communication skills.
- Excellent organizational, planning, and time-management abilities.
- Strong attention to detail, problem-solving skills, and the ability to work under pressure.
- Ability to work independently, prioritize tasks, and guide and support team members.
Location: Unit 6, 2395 Drew Road, Mississauga, L5S1T2
Schedule: Full-Time, 40 hours per week
Interested?
If you are passionate about quality, regulatory compliance, and continuous improvement, we’d love to hear from you!
