90 QA Engineering Jobs in Toronto, Canada

Role highlights

• DUTIES AND RESPONSIBILITIES The duties and responsibilities of the Quality Engineer, Automotive, are detailed below, but not limited to the…
• Hands-on experience with AIAG Core Tools (APQP, FMEA, MSA, SPC, PPAP), continuous improvement (customer support), and systemic/product qual…

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• Profile requirements: Degree in Mechanical Engineering Auditor certification, according ISO 19443 Experience in supplier quality, manufactu…
• As a Supplier Quality Engineer, your missions will include: Supporting quality clarifications with suppliers during the tender phase.

Role highlights

• As a Supplier Quality Engineer, your missions will include: Supporting quality clarifications with suppliers during the tender phase.
• Profile requirements: Degree in Mechanical Engineering Auditor certification, according ISO 19443 Experience in supplier quality, manufactu…

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• Job Responsibilities Provide Quality direction and approval to ensure all validation activities / status are conducted and maintained in ac…
• Job Summary This is a Quality position for the Richmond Hill site to ensure all GMP facilities, utility systems, equipment,…

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• Responsible for daily maintenance of test related equipment and system suitability, as required.
• Responsible for coordinating and performing assigned routine immunochemical and instrumental assays within a team environment in accordance…

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• The Opportunity: Generate and submit high-quality (CMC) regulatory documents to global health authorities .
• The Position As a CMC Regulatory Affairs Intern, you will support the preparation and global filing of critical regulatory submissions…

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• The Opportunity: Prepare global (CMC) regulatory submissions, including Module 3 CTD dossiers and electronic formatting standards .
• You will work alongside cross-functional experts to manage critical submission processes and maintain global compliance for our life-saving…

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• Coach or mentor more junior staff on document planning, processes, content, and provide peer review as needed; may oversee the…
• Required Skills: Preferred Skills: Analytics Insights, Business Writing, Clinical Research and Regulations, Clinical Trials Operations, Cop…

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• Job Description As a Engineer Specialist II you provide specialized validation knowledge and information, which is directly required to sup…
• Essential Functions: Prepare validation protocols and reports for process, packaging, or cleaning validation Monitor and coordinate manufac…

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• Responsible for daily maintenance of test related equipment and system suitability, as required.
• Responsible for coordinating and performing assigned routine immunochemical and instrumental assays within a team environment in accordance…

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• Oversight of Health, Safety, and maintenance of GMP environment Train and ensure technical staff comply with HSE requirements.
• Process improvement, development and preparation of trending reports Coordinate and schedule work of technical staff in facility, equipment…

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• Drive continuous improvement and operational excellence from a communications leadership perspective, including representing the Clinical R…
• Support the development of others in Clinical Regulatory Writing.

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• Collaborate with Quality Assurance, Manufacturing, Validation and other cross-functional teams to complete quality records within assigned…
• Compile and evaluate QC data for Annual Product Quality Reviews (APQRs) Generate quality trend reports for water system, LIR and…

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• Your Role: EMD Serono in Mississauga, Ontario is seeking a Quality Assurance Specialist.
• Manage products releases, complaints process, including deviations, investigations and documentation via Falcon (Quality Management System)…

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• Strong experience in Oncology preferred.
• Performs clinical supplies management with vendors on a country and regional level.

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• Laboratory Development Lead the design and qualification of an in-house microbiology lab to transition testing from external to internal co…
• Provide technical knowledge and leadership as the site microbiology subject matter expert (SME) (e.g. project work, resolution of deviation…

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• Job Summary Responsible for receiving and logging the samples while following cGMP requirements.
• Responsible for maintaining an accurate inventory of all laboratory supplies, samples, standards, reagents, columns and placebos, while wor…

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• Actively participate in medical writing and cross-functional meetings.
• Coach or mentor more junior staff on document planning, processes, content, and provide peer review as needed; may oversee the…

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• Actively participate in medical writing and cross-functional meetings.
• Coach or mentor more junior staff on document planning, processes, content, and provide peer review as needed; may oversee the…

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• Assess quality regulatory intelligence and global QMS changes; translate requirements into timely actions, ensuring cGMP standards are impl…
• Strong knowledge of QA systems and cGMP regulatory requirements, including importation/distribution and contract manufacturing expectations.

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• This role serves as the subject matter expert for product integrity and compliance, leading risk assessment, testing, regulatory implementa…
• Working cross-functionally with internal teams, suppliers, certification bodies, and laboratories, the role drives compliance excellence, p…

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• Continuous Improvement & Compliance Lead initiatives that improve quality system effectiveness and operational compliance.
• Coordinate responses to regulatory inspections, corporate audits, and third-party assessments.

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• Supporting the Associate Director, Country Regulatory Lead, the Regulatory Affairs Manager will lead/contribute to the development and exec…
• Principal Requirements: Responsible for managing the regulatory activities related to the assigned product portfolios.

Role highlights

• Supporting the Associate Director, Country Regulatory Lead, the Regulatory Affairs Manager will lead/contribute to the development and exec…
• Principal Requirements: Responsible for managing the regulatory activities related to the assigned product portfolios.

Role highlights

• What You’ll Do Assist in the preparation, compilation, and submission of regulatory applications for product approvals domestically and int…
• As a member of the Regulatory Affairs team, you will provide regulatory support for regulatory development and RnD software, visualization…