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Added 2 mins ago
JA
Aircraft Mechanic
JMC Aviation
Hamilton, ON
- Contract
A positive, reliable and professional approach to work
Added 2 mins ago
C
Overhead Crane Technician - FIFO 14/14
Convergint
Dartmouth, NS
- Internship
…unmatched culture, making us the #1 global, serviced-based systems integrator in the industry. We take great pride in protecting the lives and assets of our customers and their communities…
Added 17 mins ago
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Print Services Coordinator (Print Production)
BGIS
Burnaby, BC
- Full-time
…capital planning. Its range of solutions, supported by efficient systems, processes, and people, enables it to create and optimize places that work for its clients. The team is dedicated to…
Added 17 mins ago
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Systems and Applications Engineer
Valmet
Halifax, NS
- Full-time
Join Valmet as a Systems and Applications Engineer and support customers across the pulp & paper, power generation, process, marine, and minerals industries. In this customer-facing role,…
Added 17 mins ago
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Director of Sales
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- Full-time
Located in Barrie, Ontario, Prodomax is a specialized industrial engineering firm focused on designing complex automation with a blue-chip customer base since 1971. Operating from two…
Added 17 mins ago
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Bid Manager
ABOMIS
Canada
- Part-time
We are seeking a commercially minded Bid & Proposal Manager with proven experience in airport IT, aviation technology, or passenger processing systems.
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TT
Lead Mechanical CAD Designer
Tetra Tech
Thunder Bay, ON
- Full-time
…world’s most complex challenges. Our industry-leading experts in engineering and consulting are committed to driving positive change in communities around the…
Added 17 mins ago
SP
Field Service Engineer
STQ Partners
ON · Ontario, Canada
- Full-time
…directly with customers. You'll work with industrial robotic systems, supporting customers with installation, maintenance, diagnostics and technical…
Added 17 mins ago
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Intermediate I&C Technologist
Tetra Tech
Thunder Bay, ON
- Full-time
…world’s most complex challenges. Our industry-leading experts in engineering and consulting are committed to driving positive change in communities around the world. For nearly 60 years, we…
Added 17 mins ago
WI
Regional Leader, Hydro and Dams (Ontario & Atlantic)
WSP in Canada
Toronto, ON
- Full-time
With an unmatched breadth and depth of engineering, advisory and science‑based expertise, our global minds unite to power local solutions.
Added 17 mins ago
TT
Intermediate Electrical Engineer
Tetra Tech
Thunder Bay, ON
- Full-time
…world’s most complex challenges. Our industry-leading experts in engineering and consulting are committed to driving positive change in communities around the world. For nearly 60 years, we…
Added 32 mins ago
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Skywise - Business Applications & Development Tools Manager
Airbus
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- Full-time
Lead the selection, implementation, and management of tooling and systems for Business Applications across HR, Finance, Procurement, Sales, and Support.
Added 1 hour ago
Surveyor
Lloyds Register
Halifax, NS
…develop, manufacture, construct, commission, operate, and maintain engineering products, processes, systems, and…
Added 2 hours ago
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Commercial HVAC Service Technician
Captiveaire - Region 114 Western PA
PE · Prince, PE
- Full-time
Nation’s leading manufacturer of commercial kitchen ventilation systems, and now offering a complete solution of fans, heaters, ductwork and HVAC equipment. Our primary purpose is to…
Added 3 hours ago
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Certified Electrician
Parrish & Heimbecker, Limited
Halifax, NS
- Full-time
Perform preventive and corrective maintenance on plant equipment and systems, including electrical, mechanical, pneumatic, hydraulic, electromechanical, and PLC-controlled equipment.
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Commercial HVAC Service Technician
Captiveaire - Region 114 Western PA
Montreal, QC
- Full-time
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ICRH Engineer
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Toronto, ON · Greater Toronto Area, Canada
- Full-time
Stellarex Energy is seeking an experienced, technically rigorous ICRH Engineer to drive the engineering design, hardware procurement, and system integration of the Ion Cyclotron Resonance…
Added 4 hours ago
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Product Structural-Mechanical Engineer
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Calgary, AB
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Added 4 hours ago
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Manager Qualité Opérations
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Montreal, QC
- Full-time
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Service Desk Capability and Incident Manager
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Vancouver, BC
- Full-time
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IT Solution Support Engineer
Vanderlande
Vancouver, BC
- Full-time
…and operational stability. You will collaborate globally with engineering, cybersecurity, software development, service delivery, and customer…
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IT Service Delivery Manager
Vanderlande
Vancouver, BC
- Full-time
A professional degree in Computer Science, Information Technology, Information Systems, Mathematics, or a related technical field.
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IT Service Delivery Manager
Vanderlande
Vancouver, BC
- Full-time
A professional degree in Computer Science, Information Technology, Information Systems, Mathematics, or a related technical field.
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IT Solution Support Engineer
Vanderlande
Vancouver, BC
- Full-time
…and operational stability. You will collaborate globally with engineering, cybersecurity, software development, service delivery, and customer…
Added 5 hours ago
AW
Business Development Manager
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ECI

Senior R&D Engineer - Medical Device #7920

Quebec, QC, Canada

Full-time

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Job details

Job type: Full-time
Apply by: Nov 26, 2026
Experience: Minimum of 5-6 years’ direct R&D experience in medical device industry working with electromechanical devices
Posting language: English
Posted: Oct 27, 2026

Original job description

Brief Description

About ECI

ECI’s mission is to be the global leader of professional consulting services for the life sciences industry. Our clients lean on our diverse perspectives and decades of expertise to tackle their toughest challenges, and we take pride in providing them with transformative solutions with distinctive, sustainable and long-term value. ECI boasts a proven track record of providing full product life cycle consulting on a variety of challenging and exciting projects. Our collaborative culture, welcoming team and flexible employment & benefit options allow us to maintain strong relationships with the most talented individuals in the life sciences industry.

What You’ll Do

Provide quality and compliance input to project teams for decisions and deliverables (e.g., Design Change Analysis, Design Inputs, Design Outputs, Test Methods, Design Review, Design V&V, Usability Testing, Process Validation, and Labeling)
Develop quality documentation such as quality plans, standard operating procedures, and inspection procedures. Ensure regulatory, FDA, and ISO compliance in all areas of responsibilities
Represent Quality initiatives and compliance when participating and Design and Phase reviews
Serve as an effective leader and team member in supporting quality disciplines, decisions, and practices
Ensure that required standards for products are documented in the product requirements (PR) specification and ensure compliance by performing quarterly gap analysis and reviewing applicable verification documentation
Ensure the use of statistically valid sampling techniques and teach others on the use of these and other advanced statistical techniques such as DOE and ANOVA evaluations
Provide direction and lead the implementation of Acceptance Activities, First Article Inspections, In-Process Inspections, Sampling Plans, product/component testing, inspections, and acceptance criteria
Apply sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues.
Provide support for CAPA/NCRs/Complaints
Assist in special project as needed or requested

What We Look For

Bachelor’s degree in engineering or equivalent work experience
Minimum of 5-6 years’ direct R&D experience in medical device industry working with electromechanical devices
Prior experience working with Cardiac Pacemaker, associated monitoring systems and battery, Class III FDA
Experience with durable medical capital equipment in addition to single-use devices is preferred
Excellent written and verbal communication skills with good presentation and technical writing skills
Collaborative attitude with the ability to work well in a team environment
Strong engineering, design, and analysis skills along with experience with medical devices from concept to commercialization
Understanding of FDA Quality Systems Regulations
Demonstrated use of quality tools and methodologies including SPC, DOE, GR&R, FMEA, CAPA, and process validation (IQ, OQ/PQ)
Must have a good understanding of FDA 21CFR820, ISO 13485, 14971, and 11607 standards

ECI is an equal opportunity employer.

All qualified applicants will receive consideration for employment at ECI without regard to race; creed; color; religion; national origin; sex; age; disability; sexual orientation; gender identity or expression; genetic predisposition or carrier status; veteran, marital, or citizenship status; or any other status protected by law.

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More about this job

Responsibilities

Provide quality and regulatory compliance guidance across medical device design and development, including design reviews, verification and validation, usability testing, process validation, and labeling. Develop quality documentation, lead inspection and acceptance activities, apply statistical methods, and support resolution of quality issues, CAPAs, nonconformances, and complaints.

Requirements

Requires a bachelor’s degree in engineering or equivalent experience and at least 5–6 years of direct medical device R&D experience, including work with electromechanical devices. Candidates should have experience with cardiac pacemakers and related systems, knowledge of FDA and ISO requirements, and demonstrated use of quality tools such as SPC, DOE, GR&R, FMEA, CAPA, and process validation.

Skills

Medical Device R&D
Quality Systems
FDA Compliance
ISO 13485
ISO 14971
ISO 11607
Design Controls
Design Verification and Validation
Statistical Process Control
Design of Experiments
Gauge R&R
Failure Mode and Effects Analysis
CAPA
Process Validation
Acceptance Inspections
Problem Solving

Visa sponsorship

Not detected in the job text

Keywords

Medical Devices
Electromechanical Devices
Cardiac Pacemakers
Monitoring Systems
Batteries
Class III FDA Devices
FDA Quality Systems Regulations
21 CFR 820
ISO 13485
ISO 14971
ISO 11607
Design Inputs
Design Outputs
Design Reviews
Design Verification and Validation
Usability Testing
Process Validation
IQ/OQ/PQ
Statistical Process Control
Design of Experiments
ANOVA
Gauge R&R
Failure Mode and Effects Analysis
CAPA
Nonconformance Reports
Complaints
First Article Inspection
Sampling Plans
Acceptance Criteria

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