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Velan Inc.

Manager, CAPA

Montreal, QC, Canada

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Job details

Experience: 10+ years of quality engineering experience in heavy manufacturing, ideally involving valves, pumps, pressure vessels, or rotating equipment.
Posting language: English
Posted: Oct 5, 2026

Original job description

Velan 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.

Reporting to the Director, Quality assurance, the function is responsible to lead a team to deploy Corrective and Preventive Action (CAPA) program covering internal and supplier related deficiencies. You will lead cross-functional engineering, production, procurement and QC teams to investigate product failures, machining deviations, and material defects. Your role ensures our products meet strict safety and industry performance standards.

What We Offer

In addition to meaningful work that matches your ambitions and provides diverse learning opportunities, joining Velan means becoming part of a passionate team and enjoying exceptional working conditions:

Competitive salary and bonus program
Comprehensive group insurance program
24/7 telemedicine service
Employer contribution of 5% to a retirement savings plan
Competitive vacation policy
Paid holiday shutdown during the Christmas season
Reimbursement of professional association membership fees
Tuition reimbursement program
Annual gym membership reimbursement and other wellness initiatives
Free on-site parking
Company events (health, family, sports, etc.)
Fast-track career growth and professional development opportunities

Responsibilities

Program implementation: Develop a robust process for CAPA resolution to be implemented in the 3 North American plant.
Planning and prioritizing: Based on the criticality of problems, and internal customer’s needs, plan and track the issues to solve
Defect Investigation: Lead root cause analysis (RCA) for valve assembly failures, pressure test leaks, and machining non-conformances using 5 Whys, Fishbone, and FMEA.
Action Plan Development: Partner with Manufacturing, Engineering and Procurement to design corrective actions for welding, machining, assembly, and performance testing
Effectiveness Verification: Develop and execute testing protocols to verify that process changes permanently eliminate design or manufacturing defects.
Standards & Compliance: Ensure CAPA records align with industrial valve standards including ASME (Section III, B16.34), and ISO 9001.
Supplier Quality CAPA: In cooperation with the Manager, Supplier Quality, support the efforts to improve supplier’s performance. Issue and manage supplier corrective action requests (SCARs) for raw material, forging, or casting defects originating from external vendors.
KPI Management: Track quality metrics (e.g., Scrap Rate, First Pass Yield, Cost of Non-Quality) and present CAPA health reports to site leadership.

Qualifications

Bachelor’s degree in mechanical engineering, Industrial Engineering, Quality Management, or a related technical discipline.
10+ years of quality engineering experience in heavy manufacturing, ideally involving valves, pumps, pressure vessels, or rotating equipment.
Management: 3+ years in managing a team of quality specialists
Process implementation: Proven experience in implementation of CAPA process
Technical Knowledge: Understanding of non-destructive testing (NDT), geometric dimensioning and tolerancing (GD&T), manufacturing practices
Certifications: Lean Six Sigma Green/Black Belt or ASQ Certified Quality Engineer (CQE) is highly desirable.
Bilingual: French and English (Oral and written)
Ability to work under pressure and time management skills
Superior problem-solving skills.
Detail oriented
Leadership and communication abilities.
Ability to mobilize and negotiate

If you recognize yourself in this profile and are excited about this opportunity, we would be delighted to learn more about you!

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More about this job

Responsibilities

The Manager, CAPA will lead a cross-functional team to deploy and manage the Corrective and Preventive Action program across three North American plants. This role involves investigating product failures, managing supplier quality, and ensuring compliance with industrial valve standards.

Requirements

Candidates must hold a bachelor's degree in engineering or a related field and possess over 10 years of quality engineering experience in heavy manufacturing. Proficiency in CAPA processes, root cause analysis tools, and bilingualism in French and English are required.

Skills

CAPA
Root cause analysis
Mechanical engineering
Quality management
Manufacturing processes
ASME standards
ISO 9001
Non-destructive testing
GD&T
Supplier quality management
Lean Six Sigma
Leadership
Problem-solving
Communication
Negotiation
Technical reporting

Benefits

Competitive salary
Bonus program
Comprehensive group insurance
24/7 telemedicine service
Retirement savings plan
Competitive vacation policy
Paid holiday shutdown
Professional association membership reimbursement
Tuition reimbursement
Gym membership reimbursement
Wellness initiatives
Free on-site parking
Company events

Visa sponsorship

Not detected in the job text

Keywords

CAPA
Mechanical Engineering
Industrial Engineering
Quality Assurance
Root Cause Analysis
5 Whys
Fishbone
FMEA
ASME
ISO 9001
NDT
GD&T
Lean Six Sigma
ASQ
SCAR
Manufacturing
Valves
Pressure Vessels
KPI
Quality Engineering
Supplier Quality
Welding
Machining
Assembly
Performance Testing
Bilingual
Leadership
Process Implementation
Non-conformances
Heavy Manufacturing

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