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Added 2 hours ago
FI
Field Marketing Manager
Fulfillment IQ
Remote, Canada
- $75,000 to $90,000 CAD / year
- Full-time
- Remote
Report target-account attendance, held meetings, MQLs, seller response and opportunity progression at 30, 60 and 90 days with the Senior Marketing Manager, Sales and the RevOps lead.
Added 2 hours ago
FI
Content Marketing Manager
Fulfillment IQ
Remote, Canada
- $85,000 to $100,000 CAD / year
- Full-time
- Remote
Fulfillment IQ (FIQ) is a supply chain engineering and transformation company that helps brands, retailers, and 3PLs design, build, and scale high-performance logistics operations.
Added 3 hours ago
FI
Senior Marketing Manager
Fulfillment IQ
Remote, Canada
- $115,000 to $130,000 CAD / year
- Full-time
- Remote
Fulfillment IQ (FIQ) is a supply chain engineering and transformation company that helps brands, retailers, and 3PLs design, build, and scale high-performance logistics operations.
Added 3 hours ago
SA
Senior Customer Success Manager
STAN AI
Toronto, ON · North York, ON
- $100,000 to $135,000 CAD / year
- Full-time
We are looking for a Senior Customer Success Manager who is obsessed with turning users into lifelong advocates. In this role, you will own the end-to-end post-sales journey for our most…
Added 7 hours ago
RH
Contracts and Compliance Manager
Robert Half
Toronto, ON · Greater Toronto Area, Canada
- $135,000 to $150,000 CAD / year
- Full-time
Our client is seeking an experienced Contracts & Compliance Manager to oversee commercial contracts, compliance programs, and enterprise risk management across a growing manufacturing…
Added 11 hours ago
Account Manager
Amrize
AB · Calgary, AB
The Accounts Manager is responsible for building and maintaining relationships with the market’s midsized strategic account holders, while also providing pricing, technical sales support,…
Added 14 hours ago
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Service Technician
Thermon
AB · Edmonton, AB
- Full-time
You will also support the Inside Sales team by helping resolve equipment-related questions, problems, and customer concerns. This is a strong opportunity for someone with mechanical…
Added 15 hours ago
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Hussmann
Burnaby, BC
- Full-time
The Branch Operations Manager leads the day-to-day operations of a commercial refrigeration service and installation business in British Columbia. The role is responsible for managing field…
Added 19 hours ago
S
Manager, Regional Business Management and Planning (English/Spanish) - International Banking
Scotiabank
Toronto, ON
- Full-time
The Manager, Regional Business Management and Planning supports the execution of International Commercial Banking’s planning and performance management activities across the region. The…
Added 22 hours ago
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Branch Operations Manager, British Columbia
Panasonic
Burnaby, BC
- Full-time
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Added 1 day ago
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Vancouver, BC
- Full-time
We’re looking for a thoughtful, curious, and driven Sales Manager to lead a team of Commercial Account Executives focused on growing existing customer relationships. You’ll coach and…
Added 1 day ago
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Manager, Commercial Expansion
Teli Labs
Toronto, ON
- Full-time
We’re looking for a thoughtful, curious, and driven Sales Manager to lead a team of Commercial Account Executives focused on growing existing customer relationships. You’ll coach and…
Added 1 day ago
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Montreal, QC
- Full-time
Role Description The Project Manager / EV Infrastructure Specialist is a full-time, on-site role based in Montreal, QC, responsible for overseeing EV charging infrastructure projects from…
Added 1 day ago
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Engineering Lead
PERI Canada
Calgary, AB
- Full-time
Identify training needs and make recommendations to the Engineering Manager.
Added 1 day ago
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Software Development Manager
Lightspeed Commerce, Inc.
Remote, Canada
- Full-time
- Remote
Lightspeed Financial Services is looking for a Software Development Manager in North America to grow and lead our technical team within the Financial Services organization.
Added 1 day ago
Engineering Lead
PERI
Calgary, AB
Identify training needs and make recommendations to the Engineering Manager.
Added 1 day ago
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Outside Sales Representative – North/Central Alberta
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AB · Edmonton, AB
- Full-time
Make sound pricing and lead-time recommendations to support order conversion, escalating to the Western Canada Sales Manager when additional approvals or support are required.
Added 1 day ago
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Technical Inside Sales Manager
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Montreal, QC · Greater Montreal Metropolitan Area
- Full-time
The Technical Inside Sales Manager is the main point of contact for customer support within the inside sales department. This role supervises the inside sales and customer service teams for…
Added 1 day ago
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Toronto, ON
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Interns Group, Interns Group > Interim Engineering Intern - Systems
Added 1 day ago
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Concord, ON
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FY27 Intern - Software Validation Engineering Internship - Canada (16 months)
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Interns Group, Interns Group > Interim Engineering Intern - Systems
Added 1 day ago
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FY27 Intern - RF/Analog Verification Engineering Internship - Canada (4 or 16 months)
Qualcomm
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Interns Group, Interns Group > Interim Engineering Intern - HW
Added 1 day ago
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Project Manager, Calgary
GUNN Consultants
Calgary, AB
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…the project. This role is suited to an experienced Project Manager who is comfortable owning projects end-to-end and making decisions in a consulting environment. The Project Manager will…
Added 1 day ago
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Work with Operations, Mechanical Engineering, QA/QC, HSE and Sales on bids, client requirements and product roadmap.
Added 1 day ago
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Software Engineer II, Earnings
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…quality. We provide these tools across all disciplines, from Engineering and Product to Sales and Support, and are inspired by how our Toasters are already driving real value with them. The…

Fresenius Medical Care

Quality Engineer

Richmond Hill, ON, Canada

Full-time

Apply About employer

Applications open in a new tab.

Job details

Job type: Full-time
Apply by: Nov 17, 2026
Posting language: English
Posted: Nov 3, 2026

Original job description

PURPOSE AND SCOPE:

Supports FME Canada’s mission, vision, core values and customer service philosophy. Adheres to the FME Canada Compliance Program, including following all regulatory and division/company policy requirements.

Reporting to the Head of Quality, the Quality Engineer is responsible for day-to-day execution of the CAPA, nonconformance (NC) and change control processes at the Richmond Hill site. The role supports internal, MDSAP and Health Canada audits and performs product release when required. All work must comply with Canadian medical device and, where applicable, drug GMP requirements, while staying aligned with the North America and Global QMS.

DUTIES / ACTIVITIES:

CUSTOMER SERVICE:

Responsible for driving the FME Canada culture through values and customer service standards.

Accountable for outstanding customer service to all external and internal customers.

Develops and maintains effective relationships through effective and timely communication.

Takes initiative and action to respond, resolve and follow up regarding customer service issues with all customers in a timely manner.

PRINCIPAL RESPONSIBILITIES AND DUTIES:

Lead and facilitate CAPAs from initiation through effectiveness check, meeting defined timeliness targets for initiation, impact and risk assessment, and action implementation.

Run root cause investigations using structured tools (5 Whys, fishbone, fault tree, is/is-not) and document objective evidence.

Apply ISO 14971 risk principles to assess impact, risk level and the need for field action.

Define measurable effectiveness criteria and perform effectiveness checks; escalate ineffective or overdue CAPAs.

Prepare quality metrics (e.g. CAPA, audit, complaint) and trend data for site quality reviews and Management Review.

Initiate, investigate and disposition nonconforming product and process events, including supplier and distribution NCs.

Lead Material Review Board activities, segregation and quarantine, and disposition (use-as-is, return to supplier, scrap).

Trend NCs and escalate recurring or high-risk issues to CAPA.

Assess whether an NC or complaint triggers Health Canada mandatory problem reporting or a recall and support post market vigilance or product safety in filing.

Own change requests from impact assessment through implementation and closure.

Assess changes for validation, risk, labelling, supplier, training and documentation impact.

Flag changes that may be significant changes requiring a medical device licence or drug dossier amendment, and route them to Regulatory Affairs.

Ensure changes are verified as effective before closure.

-Participate in internal audits, supplier audits and MDSAP surveillance and recertification audits.

Support Health Canada establishment licence inspections, including front room / back room roles and document retrieval.

Prepare for audits through mock audits, storyboards for open CAPAs, record reviews and SME preparation.

Draft audit finding responses and track resulting CAPAs to on-time closure.

Perform batch record and documentation review and release or reject product per site procedures, once trained and delegated.

Verify distribution and traceability records are complete and accurate for released product.

For drug products, perform release activities only as delegated by the Quality Control Department under GMP requirements.

Author and revise SOPs, work instructions and forms.

Support harmonization of Canadian site processes with the North America and Global QMS and eQMS tools.

Train site personnel on CAPA, NC and change control processes.

PHYSICAL DEMANDS AND WORKING CONDITIONS:

Hybrid position requiring a minimum of 1-3 days/week in the office at the discretion of the manager.
Maximum 5-10 travel days per year (audits, conferences and meetings).

EDUCATION

Bachelor's degree in engineering, life sciences or a related technical discipline.
ASQ Certified Quality Engineer (CQE) or Certified Quality Auditor (CQA); ISO 13485 lead auditor training is preferred.

EXPERIENCE AND REQUIRED SKILLS:

Required:

Bachelor's degree in engineering, life sciences or a related technical discipline.

3–5 years in quality engineering or quality assurance in a regulated medical device or pharmaceutical environment.

Hands-on ownership of CAPA, nonconformance and change control records, including root cause analysis and effectiveness checks.

Working knowledge of the Medical Devices Regulations (SOR/98-282), ISO 13485:2016 and ISO 14971.

Experience participating in third-party or regulatory audits (MDSAP, ISO 13485, Health Canada or FDA).

Experience with an electronic QMS (for example QTRAK, Windchill, TrackWise or MasterControl).

• Strong technical writing skills in English.

Preferred

Experience with MDSAP audits and Health Canada establishment license inspections.

Drug GMP experience under Part C, Division 2, including batch record review and release.

Experience with renal, dialysis or other life-sustaining therapy products.

ASQ Certified Quality Engineer (CQE) or Certified Quality Auditor (CQA); ISO 13485 lead auditor training.

Working proficiency in French.

Core competencies

Investigative rigour: gets to verified root cause, not the first plausible one.

Risk-based judgement: sizes the response to patient and compliance risk and knows when to escalate.

Audit presence: explains records clearly and calmly to auditors and inspectors.

Ownership of timelines: drives records to on-time closure and raises slippage early.

Collaboration: works across Operations, Regulatory Affairs, Supply Chain and NA Corporate Quality.

Data literacy: builds and reads CAPA and NC trend metrics to spot systemic issues.

Relationships

Internal Contacts: Sales and Marketing, Product Safety, Post market Vigilance, Regulatory Affairs, Supply Chain and NA Corporate Quality

External Contacts: Health Canada, Vendors, Medtech Association Staff and Members

SUPERVISION:

N/A

The duties listed in this job description are intended only as illustrations of the various types of work that may be performed. The omission of specific statements of duties does not exclude them from the position if the work is similar, related, or a logical assignment to the position.

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More about this job

Responsibilities

The Quality Engineer is responsible for executing CAPA, nonconformance, and change control processes while ensuring compliance with medical device and drug GMP requirements. The role also supports internal and regulatory audits, performs product release, and maintains quality metrics for the Richmond Hill site.

Requirements

Candidates must hold a bachelor's degree in engineering or life sciences and possess 3–5 years of experience in quality engineering within a regulated medical device or pharmaceutical environment. Proficiency in ISO 13485, ISO 14971, and electronic QMS tools is required, along with strong technical writing skills.

Skills

Quality Engineering
CAPA
Nonconformance Management
Change Control
Root Cause Analysis
ISO 13485
ISO 14971
Regulatory Compliance
Medical Device Regulations
Technical Writing
Audit Support
Risk Assessment
Quality Management Systems
Data Analysis
GMP
Product Release

Visa sponsorship

Not detected in the job text

Keywords

Quality Engineer
CAPA
Nonconformance
Change Control
ISO 13485
ISO 14971
Medical Device
Pharmaceutical
GMP
Health Canada
MDSAP
Root Cause Analysis
QMS
eQMS
Regulatory Affairs
Audit
Risk Management
Technical Writing
Compliance
Quality Assurance
Validation
Material Review Board
Post Market Vigilance
SOP
CQE
CQA
Batch Record Review
Traceability
Life Sciences
Engineering

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