quality documentation

BioScript Solutions cherche un(e) spécialiste de la conformité qualité à Oakville pour gérer les documents contrôlés et les formations, soutenir les audits et assurer le respect des procédures SGQ à travers les programmes PSP, pharmacie BioScript et cliniques Coverdale.Le poste requiert expérience en gestion documentaire et formation, connaissance...

BioScript Solutions cherche un(e) spécialiste de la conformité qualité à Oakville pour gérer les documents contrôlés et les formations, soutenir les audits et assurer le respect des procédures SGQ à travers les programmes PSP, pharmacie BioScript et cliniques Coverdale.Le poste requiert expérience en gestion documentaire et formation, connaissance...

Phoenix Industrial Group of Companies is seeking a detail-oriented Quality Control Administrator to support the Quality team in implementing, maintaining, and improving the Quality Management System (QMS). The role ensures documentation aligns with client specifications, regulatory requirements, and internal quality standards.You will provide administrative...

Phoenix Industrial Group of Companies is seeking a detail-oriented Quality Control Administrator to support the Quality team in implementing, maintaining, and improving the Quality Management System (QMS). The role ensures documentation aligns with client specifications, regulatory requirements, and internal quality standards.You will provide administrative...

POSTING #: 2026-25 EMPLOYEE GROUP: CUPE, Permanent, Fulltime # Business Administration REPORTS TO: Supervisor, Quality Improvement and Records DATE POSTED: POSTING TYPE: Internal & External The organization has policies, procedures, and practices in place to ensure a response to urgent child protection matters at all times. Reporting to the...

Phoenix Industrial Group of Companies is seeking a detail-oriented Quality Control Administrator to support the Quality team in implementing, maintaining, and improving the Quality Management System (QMS). The role ensures documentation aligns with client specifications, regulatory requirements, and internal quality standards. You will provide...

BioScript Solutions cherche un(e) spécialiste de la conformité qualité à Oakville pour gérer les documents contrôlés et les formations, soutenir les audits et assurer le respect des procédures SGQ à travers les programmes PSP, pharmacie BioScript et cliniques Coverdale. Le poste requiert expérience en gestion documentaire et formation,...

Job Title: Quality Assurance Technician – DocumentationDepartment: Corporate Quality, CanadaReports to: Regional Quality ManagerPURPOSE OF THE JOBThe Quality Assurance Technician – Documentation is responsible for coordinating quality-related resources, tasks, and processes to ensure compliance with company standards and regulatory requirements. This...

Quality systems expertise defines this Documentation Specialist opportunity with Grifols, based in Winnipeg and focused on controlled records and compliance.The role provides QA support for GMP documentation processing, filing, tracking, and archiving. Reporting to the Quality Management System Manager, you will maintain the document control system and QA...

Specialist, Quality Control DocumentationRegular Tech, Admin, Office Montréal, QC, CA22 days ago Requisition ID: 1059Velan is a global leader in the design and manufacture of industrial valves. Founded in Montreal, the company is recognized for the quality of its products, its technical expertise, and its human and collaborative corporate culture.We are...

This position is listed on behalf of a partner company, which manages all applications and next steps. Our partner is looking for a Regulatory Affairs Consultant - Process & Compliance (Veeva Quality Document Management SME) based in Canada. Join a global clinical research environment where regulatory compliance and quality excellence contribute to the...

This position is listed on behalf of a partner company, which manages all applications and next steps. Our partner is looking for a Regulatory Affairs Consultant - Process & Compliance (Veeva Quality Document Management SME) based in Canada.Join a global clinical research environment where regulatory compliance and quality excellence contribute to the...

This position is listed on behalf of a partner company, which manages all applications and next steps. Our partner is looking for a Regulatory Affairs Consultant - Process & Compliance (Veeva Quality Document Management SME) based in Canada. Join a global clinical research environment where regulatory compliance and quality excellence contribute to the...

This position is listed on behalf of a partner company, which manages all applications and next steps. Our partner is looking for a Regulatory Affairs Consultant - Process & Compliance (Veeva Quality Document Management SME) based in Canada. Join a global clinical research environment where regulatory compliance and quality excellence contribute to the...

This position reports to the Quality Specialist and is responsible for QC inspections from incoming through to final inspections of outgoing orders. Documents and reports on any non-conforming materials/products and assists in investigating and resolving such issues.B - RESPONSIBILITIES AND ACTIVITIESQuality Control (85% of time)Conducts incoming...

This position reports to the Quality Specialist and is responsible for QC inspections from incoming through to final inspections of outgoing orders. Documents and reports on any non-conforming materials/products and assists in investigating and resolving such issues.B - RESPONSIBILITIES AND ACTIVITIESQuality Control (85% of time)Conducts incoming...

POLYVANTIS GmbH is seeking a Production Line Operator at its Long Sault facility. You will maintain product quality, conduct required tests, and document results. Starting pay is $24.64 per hour with planned increases to $28.51 after 12 months, with annual wage steps thereafter.The role requires adherence to safety and quality standards, accurate paperwork...

Enhance documentation processes as a Quality Control Documentation Expert at Velan located in Montréal, QC. This vital role engages with manufacturing documentation to ensure compliance and quality standards.Reporting to the Director of Quality Control, your experience of 3 to 5 years in quality control documentation will enable you to gather, check, and...

Skyfold Inc., a member of the dormakaba group, seeks an Integrated Management System & Documentation Specialist to own ISO 9001/14001 quality controls, document control, and audit coordination within our quality team.You will manage SOPs, process documentation, and supplier evaluations while supporting internal and external audits and ongoing improvements in...

OpenText in Ontario is seeking a Lead Quality Developer to ensure the accuracy and integrity of our document conversion and viewing technologies. You will lead quality initiatives across a broad portfolio of loaders and products, validating that content is preserved throughout processing workflows.This role blends technical leadership with hands-on quality...