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Added 4 hours ago
TM
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…to correct the conditions of disadvantage in employment in Canada and to bring lived experiences to the work, we encourage applications from members of equity deserving groups that have…
Added 4 hours ago
TM
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Added 8 hours ago
LD
Quality Specialist
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- Full-time
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Added 10 hours ago
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Added 12 hours ago
LD
Quality Specialist
Leonardo DRS
Bedford, QC
- Full-time
Reporting directly to the Manager-Quality, the Quality Specialist – Quality Systems coordinates the internal audit program, facilitates the organization-wide corrective action process, and…

Leonardo DRS

Quality Specialist

Bedford, NS, Canada

Full-time

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Job details

Job type: Full-time
Apply by: Nov 29, 2026
Experience: 3–5 years of experience in quality management systems, internal auditing, corrective action, or process improvement in a regulated or manufacturing environment.
Posting language: English
Posted: Oct 30, 2026

Original job description

DRS Pivotal Power, Inc. is located in Bedford, Nova Scotia. DRS Pivotal Power is a leader in the design, development and manufacture of high reliability power conversion equipment for mission critical applications supporting all branches of the military in Canada, the US and many countries abroad. All products are designed and manufactured in house by our growing team of over 150 employees. DRS Pivotal Power is part of the Leonardo DRS Naval Electronics group and has currently over 30,000 fielded units boasting a field reliability of over 99%.

Job Summary

Reporting directly to the Manager-Quality, the Quality Specialist – Quality Systems coordinates the internal audit program, facilitates the organization-wide corrective action process, and monitors the efficiency and effectiveness of quality management system processes. Working with process owners and leadership, this role uses audit results, corrective action data, and process measures to identify risks, verify that actions achieve their intended results, and support continual improvement. This is an in-office position reporting on-site at our Bedford, NS facility.

As a Quality Specialist - Quality Systems, your main responsibilities will include:

Plan and maintain a risk-informed internal audit program, including audit schedules, scope, criteria, methods, auditor assignments, and follow-up priorities.
Conduct audits through interviews, observation, and evidence review; document findings clearly and maintain controlled audit records in accordance with retention requirements.
Track audit completion and communicate findings, overdue audits, and follow-up status to process owners and leadership.
Coordinate the corrective action process for audit findings, nonconformities, customer issues, and other quality inputs. Coach action owners on containment, root-cause analysis, and action planning while process owners retain responsibility for solutions.
Monitor corrective action timeliness, verify implementation and effectiveness, and escalate overdue, recurring, or systemic issues.
Analyze audit, corrective action, and process-performance trends to identify risks and improvement priorities.
Work with process owners to establish meaningful measures of process efficiency and effectiveness, including targets, data sources, review frequency, and response thresholds. Coordinate action when results do not meet planned outcomes.
Prepare dashboards and status summaries for process reviews, tiered meetings, and management review; track resulting decisions and actions to completion.
Support cross-functional quality investigations and improvement initiatives by coordinating evidence-based analysis, documenting findings, and measuring the effectiveness of changes.
Review design changes for impacts on product conformity, inspection and test, first article inspection, controlled documentation, and quality records; provide Quality approval within assigned authority.
Improve QMS procedures, audit tools, training, and reporting methods based on lessons learned. Collaborate across functions and provide regular progress updates to the Manager–Quality.

What you require to be successful in the role:

Bachelor’s degree in Engineering, Quality, Business, or a related field, or equivalent relevant experience; considered an asset.
3–5 years of experience in quality management systems, internal auditing, corrective action, or process improvement in a regulated or manufacturing environment.
Working knowledge of ISO 9001 and AS9100 quality management system requirements and the ability to apply them to internal audits and process monitoring.
Experience planning and performing process-based audits, documenting objective evidence, reporting findings, and following up on actions.
Ability to facilitate root-cause analysis and corrective action with cross-functional teams and verify action effectiveness.
Ability to develop and interpret process measures, identify trends, and communicate findings and recommendations to process owners and leadership.
Strong organizational skills and ability to manage an audit schedule, multiple action items, deadlines, and controlled records. Proficiency with common QMS, corrective action, reporting, and data-analysis tools; experience building practical dashboards is an asset.
Excellent interpersonal, facilitation, written communication, and presentation skills; able to challenge constructively and maintain auditor objectivity.
Internal auditor training or certification and familiarity with aerospace/defense quality requirements are assets.

Benefits of working with DRS Canada:

A motivating team-based environment where your achievements matter
An opportunity to work on industry leading edge technology Flexible work hours and a compressed work week to promote a healthy work/life balance
Opportunity for Hybrid work based on operational needs Industry leading wellness program including:
Health, dental, and vision coverage available on first day of hire at no cost to the employee with access to virtual healthcare Access to Employee and Family Assistance Program Competitive compensation including:
Reimbursement for professional development initiatives and memberships plus access to free online learning resources.
Registered Retirement Savings Plan with matching company contributions with access to complimentary financial planning.
Employee Stock Purchase Program
Maternity and Parental leave top-up
Vacation, personal days, sick leave, and additional company paid days off

About DRS Pivotal Power

DRS Pivotal Power Inc., a subsidiary of Leonardo DRS, is a leader in the development and manufacture of high reliability power conversion equipment for mission critical military applications. DRS Pivotal Power is part of the Naval Electronics Canada Group.

All applicants must fulfill requirements for Canadian security clearance.

Applicants requiring a disability related accommodation to participate in the recruitment process are to advise Human Resources. DRS Pivotal Power Inc. is an equal opportunity employer.

Applicants may apply to this position online at www.leonardodrs.com/careers.

#DRSCanada

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More about this job

Responsibilities

Coordinate a risk-informed internal audit program and the organization-wide corrective action process, including documenting findings, monitoring deadlines, and verifying implementation and effectiveness. Analyze quality and process data, support investigations and improvement initiatives, review design changes for quality impacts, and report progress and results to process owners and leadership.

Requirements

The role seeks 3–5 years of experience in quality systems, internal auditing, corrective action, or process improvement in a regulated or manufacturing environment, with working knowledge of ISO 9001 and AS9100. Candidates should be able to conduct process-based audits, facilitate root-cause analysis, assess corrective action effectiveness, interpret process measures, manage controlled records, and communicate effectively; a relevant bachelor’s degree or equivalent experience is considered an asset.

Skills

Quality Management Systems
Internal Auditing
Corrective Action
Root-Cause Analysis
Process Improvement
ISO 9001
AS9100
Risk Assessment
Audit Planning
Objective Evidence Documentation
Trend Analysis
Dashboard Development
Cross-Functional Facilitation
Controlled Records Management
Quality Investigations

Benefits

Flexible Work Hours
Compressed Work Week
Hybrid Work Opportunity
Wellness Program
Health Insurance
Dental Insurance
Vision Coverage
Virtual Healthcare
Employee and Family Assistance Program
Professional Development Reimbursement
Professional Membership Reimbursement
Online Learning Resources
Registered Retirement Savings Plan With Company Matching
Financial Planning
Employee Stock Purchase Program
Maternity and Parental Leave Top-Up
Vacation
Personal Days
Sick Leave
Additional Company-Paid Days Off

Visa sponsorship

Not detected in the job text

Keywords

Quality Management System
ISO 9001
AS9100
Internal Audit Program
Process-Based Auditing
Corrective Action
Nonconformity
Root-Cause Analysis
Containment
Effectiveness Verification
Risk-Informed Auditing
Objective Evidence
Controlled Documentation
Quality Records
Process Performance Measures
Trend Analysis
Management Review
Dashboards
First Article Inspection
Product Conformity
Inspection and Testing
Aerospace and Defense
Manufacturing
Power Conversion Equipment
Continuous Improvement
Canadian Security Clearance

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