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Added 9 mins ago
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Health and Safety Coordinator – Alto Project
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Montreal, QC
- Full-time
SYSTRA Canada is part of the SYSTRA group, an international consulting and engineering group, a world leader in the design of transport infrastructures. SYSTRA Canada is an engineering and…
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Montreal, QC
- Full-time
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Montreal, QC
- Full-time
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Added 9 mins ago
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Senior Project Manager
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- Full-time
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- Full-time
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- Full-time
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IPG

Quality Specialist

Truro, NS, Canada

Full-time

Apply About employer

Applications open in a new tab.

Job details

Job type: Full-time
Apply by: Dec 5, 2026
Experience: 2-4 years of quality and/or continuous improvement experience in a manufacturing environment.
Posting language: English
Posted: Nov 5, 2026

Original job description

Join the IPG Team!

Are you ready to elevate your career? At IPG, we are more than just a global leader in packaging and protective solutions - we are a community that values safety, people, passion, integrity, performance, and teamwork. From tapes and films to packaging and protective products, as well as engineered coated materials and advanced packaging machinery, we develop innovative solutions that protect the world. Now, we are expanding our global team and looking for talented individuals like you!

Position Description

Title: Quality specialist

Department: Operations

Immediate Supervisor: Corporate Quality Director

Status: Salaried Exempt

Position Purpose: The QA Specialist is responsible for driving operational excellence and ensuring product and process quality across the site. This role integrates continuous improvement methodologies with quality assurance practices to enhance performance, reduce waste, and ensure compliance with internal and customer standards. The position works closely with site leadership, engineering, and operations teams to lead initiatives that deliver measurable improvements and maintain high-quality standards.

Principle Accountabilities

Support and Lead (as assigned) all safety programs, fostering a culture of safety and compliance throughout the organization.
Lead the implementation and sustainment of the Intertape Performance System (IPS) and drive continuous improvement initiatives across the site.
Conduct and oversee in-process and receiving inspections (raw materials and components), ensuring proper disposition, documentation, and compliance with procedures.
Investigate internal and customer nonconformances, drive root cause analysis, and implement effective corrective / preventative actions.
Maintain and continuously improve quality assurance procedures, inspection/test records, and compliance documentation in accordance with retention policies.
Manage and maintain the QC laboratory, ensuring equipment calibration, safety, efficiency, and organized workflow.
Build and sustain 5S and visual management systems across quality and operational areas.
Provide leadership, coaching, and support to cross-functional teams on continuous improvement and quality assurance methodologies.
Support customer compliance documentation and respond to ad hoc inspection/testing requests for Protective Packaging products.
Recommend and implement improvements to quality-related procedures, systems, and structures.
Ensure effective communication and change management practices across all levels of the organization to successfully impact continuous improvement and quality initiatives.
Perform other duties as assigned.

Essential Skills And Experience

Bachelor’s degree in technical field preferred (Engineering, Sciences, etc.),
2-4 years of quality and/or continuous improvement experience in a manufacturing environment.
Proficient with Microsoft Word, Excel, Access, Outlook and Teams.
Data analysis / statistical proficiency, including common software applications
Demonstrated time management and organization skills.
Ability to multi-task, deal with tight timelines, exhibit appropriate urgency in solving problems
Ability to effectively communicate ideas, results, and most impactful priorities
Proficient documentation skills. Can produce coherent, informative and intuitive content (both technical and nontechnical)

Why Choose IPG?

At IPG, you will find more than just a job - you will find a place where your success is our success. We pride ourselves on a culture built around strong relationships, where every team member plays a crucial role in our growth. Whether it is through cross-department collaboration, continuous training, or sustainability-driven initiatives, we create an environment where you can thrive.

Our commitment to sustainability influences everything we do, from designing eco-friendly products to minimizing waste in our production processes. We are dedicated to building a greener future while providing safe, supportive workplaces for our people.

With over 40 years of industry expertise and a proven track record of growth and innovation, IPG offers a stable, secure environment where you can flourish!

We offer competitive pay, extensive benefits that support you and your family, and exciting career development opportunities. Whether you are looking to enhance your skills or advance your career, we offer ongoing training and the support you need to succeed. Think big, dream bigger, and make an impact with IPG.

You belong here. Join us today!

Apply About employer

More about this job

Responsibilities

Lead site quality assurance and continuous improvement initiatives, including inspections, nonconformance investigations, corrective actions, and compliance documentation. Maintain the QC laboratory and quality systems while coaching cross-functional teams and supporting customer compliance requests.

Requirements

A technical bachelor's degree is preferred, along with 2–4 years of quality and/or continuous improvement experience in manufacturing. Candidates should have data and statistical analysis skills, proficiency with Microsoft Office applications, strong documentation and communication abilities, and the capacity to manage multiple priorities and tight timelines.

Skills

Quality Assurance
Continuous Improvement
Root Cause Analysis
Corrective And Preventive Actions
In-Process Inspection
Receiving Inspection
Data Analysis
Statistical Analysis
Microsoft Office
Documentation
Time Management
Organization
Communication
Change Management
5S
Visual Management

Benefits

Competitive Pay
Extensive Benefits
Career Development Opportunities
Ongoing Training

Visa sponsorship

Not detected in the job text

Keywords

Quality Assurance
Quality Control
Continuous Improvement
Intertape Performance System
Manufacturing
Operational Excellence
Product Quality
Process Quality
Safety Programs
In-Process Inspection
Receiving Inspection
Raw Materials
Nonconformance
Root Cause Analysis
Corrective Actions
Preventive Actions
Compliance Documentation
Inspection Records
QC Laboratory
Equipment Calibration
5S
Visual Management
Customer Compliance
Data Analysis
Statistical Analysis
Microsoft Word
Microsoft Excel
Microsoft Access
Microsoft Outlook
Microsoft Teams

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