Top QA Jobs in Vancouver

Supports plant quality and food safety programs through SOP reviews, deviation resolution, microbiology testing, product specifications, labeling, audits, HACCP updates, KPI and trend reporting, training, supplier and pest-control oversight, and audit preparation. Provides backup for the HACCP Coordinator and QA Technicians while coordinating inspections, facility maintenance follow-up, documentation, and continuous improvement activities.

Lead QA and Sanitation teams to ensure food safety and regulatory compliance. Maintain HACCP procedures, conduct audits and investigations, manage corrective actions, metrics, vendor relationships, budgets, and continuous improvement for Vancouver operations.

Coordinates quality compliance and certification initiatives for natural health and pharmaceutical products. Responsibilities include maintaining quality agreements, investigating complaints and adverse reactions, tracking CAPAs, conducting trend analysis, monitoring licensing and certification updates, liaising with stakeholders, and maintaining SOPs in accordance with cGMP and pharmacovigilance practices.

Build and lead customer operations training and quality assurance programs. Design curricula, quality rubrics, calibration processes, knowledge-base content, and onboarding programs; identify skill gaps through QA and performance data; measure training impact; conduct root-cause analysis; improve workflows; support compliance; and influence leaders across internal and outsourced teams.

Plans and executes system, integration, regression, and user acceptance testing across software, data, interfaces, billing, and communication solutions. Reviews requirements for testability, identifies risks, prepares test data, manages defects, verifies fixes, documents testing evidence, and communicates quality status to stakeholders. Collaborates with analysts, developers, project managers, operations, and clients while supporting multiple change initiatives and improving QA processes.

Performs manual and automated QA testing for Acturis and other software systems. Creates test plans, scenarios, scripts, datasets, and traceability matrices; executes tests, analyzes results, troubleshoots issues, manages defects through resolution, and produces test reports. Collaborates with developers, business analysts, project managers, vendors, and business stakeholders throughout the software development lifecycle, while participating in testing meetings and providing quality guidance.

Manually test Shopify eCommerce stores for design, functionality, and responsive behavior. Verify pages against Figma and project requirements, use DevTools to inspect and debug, document and report bugs, collaborate with developers/PMs/designers, and suggest fixes for recurring issues to ensure flawless launches.

Own and evolve the company-wide Quality Engineering strategy, standards, automation architecture, tooling, quality metrics, and release controls. Assess maturity across engineering domains, drive risk-based testing and shift-left practices, lead critical investigations, and guide QA Technical Leads. The role remains hands-on through code, prototypes, architecture reviews, and pilots involving UI and backend automation, CI/CD, cloud-native environments, observability, and emerging technologies including AI.

Own end-to-end product quality through manual exploratory testing, automation, release validation, API and data verification, regression testing, and bug management. Build and maintain UI and API automation using Playwright or Cypress, integrate tests into CI/CD, validate data flows across application layers, and collaborate with engineering, product, design, business, and customer success teams in a fast-paced Agile environment.

Lead quality engineering for a cloud-native Workforce Management and Customer Experience platform. Responsibilities include building full-pyramid automated test frameworks, testing Java microservices and APIs, validating contracts and distributed systems, conducting performance tests, integrating automation into CI/CD quality gates, and testing forecasting and scheduling functionality. The role also involves defect analysis, quality standards development, and collaboration with engineering, architecture, product, and business stakeholders.

Supports product compliance and quality assurance for furniture and consumer goods. Reviews packaging, labeling, documentation, certificates, test reports, and specifications for Canadian regulatory conformity. Conducts product inspections and testing, controls assembly instructions, investigates defects and customer issues, coordinates corrective actions with suppliers and internal teams, and processes defective product and spare-parts requests.

Provides QA support for GMP drug substance manufacturing and quality control operations. Reviews batch records, raw data, procedures, and documentation for compliance and data integrity; performs ERP materials release; supports deviations, investigations, CAPAs, change controls, risk assessments, audits, and inspections. Maintains inspection readiness and helps ensure clinical batches meet cGMP requirements across internal and external manufacturing, testing, packaging, and labeling operations.

Reviews and dispositions cGMP QC laboratory data supporting biologics clinical manufacturing. Responsibilities include approving qualification and validation documentation, investigating data issues and OOS/OOT results, supporting deviations, CAPAs, change controls, regulatory submissions, inspections, and audit readiness. The role partners cross-functionally to maintain data integrity, compliance, and quality across QC operations.

Conducts QA compliance and accuracy reviews of batch records, logbooks, and electronic manufacturing documentation for internal and external biopharmaceutical operations. Provides real-time manufacturing-floor quality support, coordinates corrections and final batch packages, releases materials in ERP, reviews equipment records, and supports deviations, CAPAs, change controls, inspections, audits, risk assessments, and continuous improvement. The role ensures cGMP, data integrity, and regulatory compliance across clinical drug substances, products, devices, and combination products.

Provides quality oversight of contract manufacturing organizations and suppliers supporting monoclonal antibody programs. Responsibilities include CMO qualification, quality agreements, GMP audits, deviations, CAPAs, batch record review, batch disposition, risk assessments, inspection readiness, regulatory support, and continuous improvement. Acts as an on-site quality authority during manufacturing campaigns and collaborates with cross-functional teams and external partners.

Manage supplier quality across the lifecycle for materials, equipment, and services supporting biopharmaceutical development and manufacturing. Responsibilities include supplier qualification, quality agreements, deviations, change management, complaints, risk assessments, performance monitoring, continuous improvement, audit and inspection readiness, and regulatory compliance. The role partners with Procurement, Operations, QC, Supply Chain, and Process Development while maintaining supplier records, quality events, and audit reports in electronic quality and enterprise resource systems.

Lead QA strategy and automation across Knotch’s products, building scalable testing frameworks, API validation, CI/CD integrations, coverage metrics, and AI feature evaluation. Manage offshore QA staff, hire a US-based team, perform manual and performance testing, investigate root causes, and collaborate with engineering and product teams to improve quality and release confidence.

Drive quality assurance for web features from technical handoff through production release. Responsibilities include test planning, test case creation, functional and exploratory testing, regression, UI/UX, cross-browser, responsive, API, and end-to-end testing. Support releases through build validation and monitoring, document and review tests, collaborate with product and engineering teams, improve QA metrics, and optionally contribute to test automation.

Supports DO-178C and DO-254 certification activities, SQA audits, compliance checks, certification artifact preparation, configuration management, change control, traceability, and evidence-package maintenance. The role works with engineering and certification teams to ensure safety-critical software processes and deliverables meet standards, assists with audits, tracks gaps and review closures, and improves repeatable quality workflows. It also provides focused support for safety-relevant verification and offers development toward a long-term certification and SQA career.

Design and execute manual and automated QA testing across web, desktop, and mobile applications. Create test plans, perform exploratory testing, maintain end-to-end regression suites, investigate failures, assess release risk, and validate deployments. Collaborate with Product, Design, and Engineering to improve testability and quality practices. Use AI tools such as Cursor and Claude while independently verifying their output.

Audits study data, reports, facilities, SOPs, and documentation for GLP compliance; tracks CAPAs and deviations; conducts internal audits and regulatory training; maintains vendor qualifications; and supports client and regulatory audits.

Coordinates laboratory quality assurance and quality control activities, including QMS documentation, ISO/IEC 17025 compliance, audits, proficiency testing, CAPA tracking, method validation, equipment and chemical logs, and continuous improvement. The role supports laboratory safety, technical calculations, data entry, stakeholder coordination, and special projects while ensuring adherence to quality and inspection requirements.

Executes quality assurance programs for Canadian distribution facilities, including audits, procedures, training, inspections, testing, product release, rework, relabeling, and NC/CAPA investigations. Maintains quality metrics, supports regulatory compliance, provides guidance to operations, and collaborates with cross-functional teams to resolve quality issues. The role requires knowledge of Health Canada regulations, medical device and drug regulations, GMP, and related product regulations.

Build and maintain scalable automated UI and API test suites using Playwright, integrate testing into CI/CD, and drive end-to-end quality across platform initiatives. Collaborate with architects, developers, product managers, delivery leaders, and QA specialists to define acceptance criteria, prioritize coverage, support UAT, improve testing processes, and standardize quality practices. The role emphasizes automation architecture, hands-on coding, continuous testing, and applying AI to improve test development and maintenance.

Lead automation design and implementation for integrations: build and maintain scalable Playwright E2E suites, integrate tests into CI/CD, drive UI and API test strategy, collaborate with architects and product to define acceptance criteria, support UAT, and improve QA processes and documentation.