Find work in Canada.

358,856 jobs across our Canadian network. How we count

Jobs in Canada

25+ jobs

Email me new jobs Save this search

Added 1 hour ago
J
Civil Engineer - Design and Project Management, Urban Infrastructure, Greater Montreal Area
JobsMedia.io
Montreal, QC
- Full-time
Contribute to the preparation of service proposals and the development of business relationships
Added 1 hour ago
QT
Senior Account Manager
Quest Talent Search Solutions Ltd.
Vancouver, BC · Greater Vancouver, BC
- $75,000 to $85,000 CAD / year
- Full-time
5+ years of experience in account management, customer success, business development, or client relationship management within logistics, transportation, warehousing, or supply chain
Added 1 hour ago
J
Commercial Insurance Director
JobsMedia.io
Toronto, ON
- Full-time
Partner with producers, account management teams, and insurance markets to deliver strong client outcomes.
Added 1 hour ago
FH
Project Manager - Redevelopment & Major Projects
Fraser Health Authority
Surrey, BC
- $46.37 to $66.66 CAD / hour
- Full-time
Partner with sponsor clients in developing and delivering capital development presentations, briefings, reports, and status updates.
Added 2 hours ago
SM
RQ11706 – Software Developer – Senior
S M Software Solutions Inc
Toronto, ON
- Full-time
Client: Ministry of Public and Business Service Delivery and Procurement – RQ11706
Added 2 hours ago
SM
RQ11706 – Software Developer – Senior
S M Software Solutions Inc
Toronto, ON
- Full-time
Client: Ministry of Public and Business Service Delivery and Procurement – RQ11706
Added 2 hours ago
SM
RQ11706 – Software Developer – Senior
S M Software Solutions Inc
Toronto, ON
- Full-time
Client: Ministry of Public and Business Service Delivery and Procurement – RQ11706
Added 3 hours ago
Client Executive
XenTegra
ON
We are looking for a results-driven Client Executive to own and grow a mid-market commercial territory across the province of Ontario. This is an outside sales role for a seasoned…
Added 3 hours ago
Account Manager
SJR
Toronto, ON
Support strategy development and client presentations (ideas, programs, budgets, etc.)
Added 4 hours ago
WI
Senior Archaeologist
WSP in Canada
Mississauga, ON
- Full-time
Support business development through proposal development, relationship building, and strategic insight.
Added 4 hours ago
WI
Senior Archaeologist
WSP in Canada
Burlington, ON
- Full-time
Support business development through proposal development, relationship building, and strategic insight.
Added 4 hours ago
W
Principal Process Automation Engineer
Worley
Toronto, ON
- Full-time
We partner with our customers to find solutions that create value over the life of their assets. We implement new technologies to run assets more efficiently, secure and safeguard social…
Added 4 hours ago
WG
Accounting Analyst
Walter Group
Westmount, QC
- Full-time
…handle the full accounting cycle of the partnerships and general partner entities, support fund and corporate accounting more broadly, contribute to financial software implementations, and…
Added 4 hours ago
RP
Project Manager
RECRUITMENT PARTNERS INC.
AB · Edmonton, AB
- Full-time
…are proud of our team of consultants, who come with practical business experience, a strong network of professional contacts, and are focused on what is best for both clients and…
Added 4 hours ago
RP
Personal Benefits Consultant
RECRUITMENT PARTNERS INC.
AB · Edmonton, AB
- Full-time
…are proud of our team of consultants, who come with practical business experience, a strong network of professional contacts, and are focused on what is best for both clients and…
Added 4 hours ago
PC
Finance Transformation Manager, Enterprise Performance Management (EPM) (Bilingual FR/EN)
Pwc Canada
Calgary, AB · Montreal, QC · Ottawa, ON
- Full-time
…work as part of a team of problem solvers, helping to solve business issues, deliver high quality client service and operational efficiency. Responsibilities include but are not limited…
Added 4 hours ago
18 Month Contract People & Culture - Human Resources Business Partner
Laurentis Energy Partners
Oakville, ON
Laurentis is seeking dynamic talent to join our team in the role of Human Resources Business Partner, working closely the People & Culture (P&C) team. The ideal candidate would have 8-10…
Added 4 hours ago
CI
Business Auditor
Cowan Insurance Group
Hamilton, ON · Brantford, ON · Cambridge, ON
- Full-time
Assessing and evaluate business, operational, compliance, and errors & omissions (E&O) risks within Commercial and/or Personal Insurance operations, understanding business risks related to…
Added 4 hours ago
CI
Claims Specialist
Cowan Insurance Group
Hamilton, ON · Brantford, ON · Cambridge, ON
- Full-time
A collaborative approach and the ability to build effective relationships with clients, insurers, adjusters, legal counsel, vendors, and internal business partners
Added 4 hours ago
CI
Commercial Account Assistant
Cowan Insurance Group
Cambridge, ON
- Full-time
Cowan Insurance Group is looking for a Commercial Account Assistant to join our Small Business Solutions (SBS) Team!
Added 4 hours ago
K
Senior Product Manager, Integrations
Kindsight
Remote, Canada
- $105,000 to $140,000 CAD / year
- Full-time
- Remote
…Design, Engineering and 3rd party teams to ensure alignment. Partner with Engineering to create robust technical plans, improve development speed, and resolve execution challenges.…
Added 4 hours ago
K
Senior Director, Solutions Engineering
Kindsight
Remote, Canada
- $240,000 to $280,000 CAD / year
- Full-time
- Remote
Partner closely with Sales and Client Success leadership to align demo strategy with account priorities, expansion opportunities, and deal strategy.
Added 4 hours ago
K
Enterprise Account Executive
Kindsight
Remote, Canada
- $260,000 to $320,000 CAD / year
- Full-time
- Remote
Partner with Solutions Engineering, Customer Success, Professional Services, and leadership to ensure seamless client experiences.
Added 4 hours ago
K
Enterprise Account Executive, Community Foundations
Kindsight
Remote, Canada
- $280,000 to $320,000 CAD / year
- Full-time
- Remote
Cross-Functional Execution: Partner closely with Solutions Engineering, Professional Services, Customer Success and Revenue Operations to set clear project scopes, deliver initial customer…
Added 4 hours ago
Wealth Advisor
Sonance Wealth Partners
Edmonton, AB
You will manage and grow a portfolio of high-net-worth client relationships, deliver comprehensive financial advice and implement sophisticated investment solutions. Working with a broad…

Exquisite Biomedical Consulting

Regulatory Affairs Associate

Vancouver, BC, Canada

Part-time

Apply About employer

Applications open in a new tab.

Job details

Job type: Part-time
Apply by: Nov 8, 2026
Experience: 4+ years of regulatory affairs experience in medical devices or related life sciences products.
Posting language: English
Posted: Oct 9, 2026

Original job description

About the Company

Exquisite Biomedical Consulting (EBC) is a boutique life sciences consultancy firm specializing in Medical Affairs, Clinical and Regulatory Strategy, and Evidence Generation for medical device, regenerative medicine, diagnostics, and digital health companies.

We partner with life sciences manufacturers from concept through commercialization of novel medical products and offer services such as fractional Chief Medical Officer, medical, clinical and regulatory strategy, literature and evidence development, medical writing, and business development. Our clients range from small to midsize enterprise, start-ups and corporations in different therapeutic areas.

Role Overview

The Regulatory Affairs Associate supports EBC's clients with regulatory strategy, submissions, and lifecycle documentation for medical devices and related life sciences products. You'll turn regulatory requirements into clear plans and practical deliverables across different technologies, therapeutic areas, and development stages, and across frameworks including Health Canada, US FDA, and EU MDR.

You'll assess requirements, identify gaps, coordinate subject matter experts, prepare accurate documentation, and lead client interactions, escalating when additional or external input is needed. You'll report to the CEO and work closely with EBC's team and clients. Workload and scope vary with client needs and may include work beyond regulatory affairs, as well as internal EBC projects.

Key Responsibilities

Advise clients on regulatory needs and high-level strategy.
Develop regulatory strategies, assess product classification and pathways, and identify documentation requirements and gaps.
Prepare and review submissions and technical documentation with expert input.
Write regulatory documents, including EU MDR clinical evaluations and Clinical Study Reports.
Coordinate client-approved communications with regulators and notified bodies.
Monitor regulations, guidance, and standards, and advise the team and clients on their implications.
Ensure document accuracy and consistency, follow EBC and client procedures, and keep clear records.
Manage client projects, meet deadlines, and communicate progress and issues promptly.
Escalate when additional or external input is required.
Contribute to internal EBC projects and support the company's growth.
Protect confidential information and maintain professional, ethical conduct.

Qualifications

Must have

Bachelor's degree or higher in a science, engineering, or health field (master's or PhD preferred).
4+ years of regulatory affairs experience in medical devices or related life sciences products.
Working knowledge of FDA, Health Canada, EU, and international regulatory frameworks.
Strong writing, presentation, and negotiation skills, with the ability to turn dense regulatory text into clear business steps.
Experience preparing and reviewing regulatory documentation and coordinating input from clinical, quality, engineering, and other teams.
Familiarity with quality procedures and medical device lifecycle requirements.
Permanent authorization to work in Canada.

Nice to have

Experience with Health Canada device license applications, US FDA submissions, or EU MDR technical documentation.
Experience writing CEPs, CERs, SSCPs, PMS, PMCF, PSURs, or similar documents.
Clinical trial regulatory documentation experience.
Familiarity with ISO 13485, ISO 14971, MEDDEV and MDCG guidance, and other relevant standards.
Background in diagnostics, digital health, regenerative medicine, pharmaceuticals, or consulting.

Skills and Competencies

Regulatory research, analytical thinking, and problem-solving.
Clear writing, editing, presentation, and quality control; proficiency in Microsoft Office.
Professional, confident, and discreet in client interactions.
Organized, dependable, and responsive, with a sense of urgency.
Self-motivated and adaptable to shifting workloads and priorities.
Collaborative and willing to take on varied assignments.

What We Offer

Meaningful regulatory, clinical, and evidence-generation work at a growing boutique life sciences consultancy.
Exposure to innovative medical device, biotech, diagnostics, and healthcare projects.
A flexible, entrepreneurial environment.
Collaboration with experienced professionals across disciplines.
The chance to shape EBC's growth and effectiveness.

Apply About employer

More about this job

Responsibilities

Advise clients on regulatory strategy, product classification, pathways, documentation requirements, and gaps across FDA, Health Canada, and EU frameworks. Prepare and review regulatory submissions and technical documents, coordinate client and expert input, monitor regulatory changes, manage project delivery, and contribute to internal company initiatives.

Requirements

Requires a bachelor's degree or higher in a science, engineering, or health field, with a master's degree or PhD preferred, and at least four years of regulatory affairs experience in medical devices or related life sciences products. Candidates must have working knowledge of FDA, Health Canada, EU, and international frameworks, strong documentation and communication skills, relevant cross-functional experience, and permanent authorization to work in Canada.

Skills

Regulatory Strategy
Regulatory Submissions
Regulatory Research
Medical Device Classification
Regulatory Pathway Assessment
Technical Documentation
Clinical Evaluation
Clinical Study Reports
Regulatory Writing
Project Management
Client Communication
Quality Control
FDA Regulations
Health Canada Regulations
EU MDR
ISO 13485

Benefits

Flexible Work Environment
Cross-Disciplinary Collaboration
Exposure to Innovative Projects

Visa sponsorship

Not detected in the job text

Keywords

Medical Devices
Life Sciences
Regulatory Affairs
Regulatory Strategy
FDA
Health Canada
EU MDR
International Regulatory Frameworks
Regulatory Submissions
Technical Documentation
Clinical Evaluation Plans
Clinical Evaluation Reports
Summary of Safety and Clinical Performance
Post-Market Surveillance
Post-Market Clinical Follow-Up
Periodic Safety Update Reports
Clinical Study Reports
Clinical Trial Regulatory Documentation
ISO 13485
ISO 14971
MEDDEV
MDCG Guidance
Quality Procedures
Medical Device Lifecycle
Regulatory Research
Microsoft Office
Diagnostics
Digital Health
Regenerative Medicine

Report this job