Quality Assurance Manager

Employbridge; Mississauga; On-site; CAD 65,000 - 75,000; Full time

Job summary

A reliable packaging solutions provider is seeking an experienced QA Manager to oversee their Quality Management System and ensure compliance with regulatory standards. The ideal candidate will have a Bachelor's degree in a related field and at least 2 years of experience in GMP-regulated manufacturing. Key responsibilities include managing quality processes, leading audits, and training staff. The salary ranges from $65,000 to $75,000 annually.

Qualifications

• 2+ years of quality experience in GMP-regulated manufacturing.
• Strong knowledge of GMP, HACCP, CAPA, deviation handling.
• Certification in Quality Auditing (CQA) or Six Sigma is a plus.

Responsibilities

• Oversee Quality Management System and ensure compliance.
• Lead internal audits, CAPAs, and support external audits.
• Train and mentor staff on quality standards.

Skills

GMP compliance

Auditing

Root cause analysis

Leadership

Communication

Education

Bachelor’s degree in Chemistry, Biology, Engineering

Tools

Microsoft Office

ERP systems (SAP, Sage)

Job description

Reliable packaging solutions provider in Louisville, KY is seeking a experienced and talented QA Manager to join their team!

Salary $65-75k annually

Days

Responsibilities

• Oversee the site’s Quality Management System (QMS) and ensure compliance with GMP, customer specifications, and internal standards.
• Lead internal audits, CAPAs, and support external audits (regulatory and customer).
• Manage quality control processes, including incoming raw material inspection, in-process checks, and finished product testing.
• Develop and maintain Standard Operating Procedures (SOPs) and ensure consistent adherence.
• Lead investigations into customer complaints, non-conformances, and deviations.
• Oversee batch record review and release of finished goods.
• Train and mentor staff on GMP, quality standards, and root cause analysis techniques.
• Collaborate with production, sanitation, maintenance, and R&D to ensure quality is built into processes from end to end.
• Manage and calibrate testing equipment and laboratory processes.
• Maintain GMP documentation and ensure audit readiness at all times.
• Support environmental monitoring, allergen control, and sanitation verification programs as needed.

Qualifications

• Bachelor’s degree in Chemistry, Biology, Engineering, or related field (required)
• 2+ years of quality experience in GMP-regulated manufacturing, preferably in household chemicals, personal care, food, pharma, or related
• Strong knowledge of GMP, HACCP, CAPA, deviation handling, and root cause analysis
• Experience with regulatory inspections, customer audits, and third-party certifications
• Excellent communication, organization, and leadership skills
• Proficient in Microsoft Office; experience with ERP systems (SAP, Sage, etc.) is a plus
• Certification in Quality Auditing (CQA), Six Sigma, or related disciplines is a plus
• Proficient in Microsoft Office; experience with ERP systems (SAP, Sage, etc.) is a plus
• Certification in Quality Auditing (CQA), Six Sigma, or related disciplines is a plus