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Manager Biomedical Engineering Jobs in Quebec (NOW HIRING)

Orthosoft Inc.

Systems Designer

Montreal, QC · On-site

Risk Management Plan, * Act as a leader for Verification & Validation (V&V) Plans and usability ... Biomedical engineering is an asset. * Experience in product development and release from early ...

Alimentiv

Statistician

Sherbrooke, QC · Remote

Carry out statistical analyses and provide direction to programmers, using standard software ... Work with data management team to ensure data captured incorporates and corresponds to project ...

Alimentiv

Statistician

Montreal, QC · Remote

Carry out statistical analyses and provide direction to programmers, using standard software ... Work with data management team to ensure data captured incorporates and corresponds to project ...

Alimentiv

Statistician

Quebec, QC · Remote

Carry out statistical analyses and provide direction to programmers, using standard software ... Work with data management team to ensure data captured incorporates and corresponds to project ...

Gehc

Field Services Representative

Montreal, QC · On-site

Manage repair parts cycle times to business targets * Maintain customer service logs and internal ... Technical Diploma in Electronics Engineering or equivalent experience or training. * Candidate ...

All JobsBiomedical Engineering JobsManager Biomedical Engineering JobsManager Biomedical Engineering Jobs in Quebec

Manager Biomedical Engineering information

See Quebec salary details

$30K

$103.3K

$162K

How much do manager biomedical engineering jobs pay per year?

As of Sep 10, 2026, the average yearly pay for manager biomedical engineering in Quebec is $103,271.00, according to ZipRecruiter salary data. Most workers in this role earn between $67,000.00 and $147,000.00 per year, depending on experience, location, and employer.

What does a manager biomedical engineering do?

A Manager of Biomedical Engineering oversees the maintenance, repair, and proper functioning of medical equipment within healthcare facilities. They lead a team of biomedical engineers and technicians, ensuring that all equipment meets regulatory standards and operates safely. Their role also involves budgeting, training staff, implementing new technologies, and collaborating with other departments to support patient care. They play a critical role in ensuring that healthcare providers have reliable and effective tools for diagnosis and treatment.

What are the key skills and qualifications needed to thrive as a manager biomedical engineering?

To thrive as a Manager Biomedical Engineering, you need a solid background in biomedical engineering principles, project management, and typically a bachelor’s or master’s degree in biomedical engineering or a related field. Familiarity with regulatory standards (such as FDA, ISO 13485), medical device software, and equipment management systems is essential. Leadership, problem-solving, and effective communication are crucial soft skills for managing teams and collaborating across departments. These skills ensure the safe, efficient operation of medical technology, compliance with regulations, and the delivery of high-quality healthcare solutions.

How does a manager biomedical engineering typically collaborate with clinical staff and other departments within a healthcare facility?

A Manager of Biomedical Engineering regularly works with clinical staff, such as nurses and physicians, to understand their equipment needs, address maintenance concerns, and ensure medical devices operate safely and effectively. They also coordinate with procurement, IT, and facilities teams to manage equipment installations, upgrades, and compliance with regulatory standards. Effective communication and proactive relationship-building are crucial in this role to minimize equipment downtime and support optimal patient care.

What is the difference between Manager Biomedical Engineering vs Biomedical Equipment Technician?

AspectManager Biomedical EngineeringBiomedical Equipment Technician
CredentialsBachelor's or Master's in Biomedical Engineering; Leadership experienceAssociate's or Bachelor's in Biomedical Technology; Certification preferred
Work EnvironmentHealthcare facilities, R&D departments, management rolesHospitals, clinics, service centers, equipment maintenance
Employer & IndustryHospitals, medical device companies, research institutionsHospitals, clinics, biomedical service providers

The Manager Biomedical Engineering oversees biomedical equipment management, staff, and strategic planning, focusing on leadership and project management. In contrast, a Biomedical Equipment Technician primarily handles the maintenance, repair, and calibration of medical devices. While both roles require technical knowledge, the manager position emphasizes leadership and administrative skills, whereas the technician role is more hands-on with equipment servicing.

What are the most commonly searched types of Biomedical Engineering jobs in Quebec?

The most popular types of Biomedical Engineering jobs in Quebec are:

What cities in Quebec are hiring for Manager Biomedical Engineering jobs?

Cities in Quebec with the most Manager Biomedical Engineering job openings:

Manager Biomedical Engineering jobs near you
Infographic showing various Manager Biomedical Engineering job openings in Quebec as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 81% Physical, 3% Hybrid, and 16% Remote job distribution, with an average salary of $103,271 per year, or $49.6 per hour.

Senior Design Quality Engineer / Ingenieur principal en qualite de la conception

Montreal, QC • Hybrid

Boston Scientific
Medical Equipment and Supplies Manufacturing • 10K+ employees
Learn more about Boston Scientificexternal

Full-time

Re-posted 7 days ago

Boston Scientific rating

8.5

Company rating: 8.5 out of 10

Based on 120 frontline employees who took The Breakroom Quiz

Job description

Additional Location(s): Canada-QC-Montreal

Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance

At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we'll help you in advancing your skills and career. Here, you'll be supported in progressing - whatever your ambitions.

Diversite - Innovation - Bienveillance - Collaboration mondiale - Esprit gagnant - Bienveillant - Haute performance

Chez Boston Scientific, nous vous donnerons l'opportunite d'exploiter tout ce qui est en vous en travaillant dans des equipes d'employes diversifies et hautement performants, pour relever certains des defis les plus importants de l'industrie de la sante. Grace a l'acces aux derniers outils, informations et formations, nous vous aiderons a faire progresser vos competences et votre carriere. Ici, vous serez accompagne dans votre progression - quelles que soient vos ambitions.  

French translation to follow

About the role: 

We have a high-impact opportunity for a Senior Design Quality professional to lead design assurance efforts for a critical medical device in the Electrophysiology space. This role requires a self-driven professional capable of independently managing complex technical challenges and driving to solutions across hardware, software, and system domains. The Senior Design Quality role will influence strategic quality initiatives, mentor junior engineers, and serve as a key resource in cross-functional teams to ensure product safety, regulatory compliance, and design robustness. 

Work mode:

At Boston Scientific, we value collaboration and synergy. This hybrid role is based at the Montreal, Canada location and requires being on-site at least three (3) days per week.

Visa Sponsorship:  

Boston Scientific will not offer sponsorship or take over sponsorship of an employment VISA for this position at this time.  

Your responsibilities will include: 

  • Serve as the technical authority within Quality for system integration, design decisions, risk management, and software development & validation. 
  • Independently lead design control activities for the Capital Equipment, including Design & Development planning, risk management, design verification, and validation efforts, with a strong focus on robustness of system design and documentation. 
  • Collaborate closely with R&D, regulatory, manufacturing, and clinical teams  to provide expert guidance on design and compliance matters throughout the product lifecycle. 
  • Own and maintain comprehensive risk management files (Hazard Analysis, FMEAs), ensuring robust coverage of both hardware, software, and system risks, applying advanced risk mitigation strategies to influence robust design decisions 
  • Lead root cause investigations and resolution of test failures, CAPAs, NCEPs, and complaints, driving corrective actions and preventive measures with minimal oversight. 
  • Provide mentorship and guidance to junior engineers on design assurance best practices, regulatory requirements, and quality processes. 
  • Proactively identify gaps and opportunities for continuous improvement in product development processes, tools, and documentation. 
  • Act as a primary point of contact for design assurance during internal and external audits and regulatory inspections. 
  • Effectively manage multiple priorities and projects independently, demonstrating strong decision-making skills in ambiguous situations, and ability to influence project team towards quality-centric decisions and behaviors

Required qualifications 

  • Bachelor's degree in Mechanical, Electrical, Software Engineering, Biomedical Engineering, or related technical discipline. 
  • 7+ years of experience in Quality Assurance, Design Assurance, Software Quality, or related roles in the medical device industry. 
  • Demonstrated expertise in Design Controls, Risk Management (ISO 14971), Quality System Regulations (21 CFR 820), and Quality management systems (ISO 13485).
  • Proven ability to independently lead complex product development projects, including software and system quality assurance activities, from inception through completion. 
  • Experience developing and maintaining risk documentation such as FMEAs and Hazard Analyses with a hardware, software and system focus. 
  • Strong problem-solving skills with experience leading root cause analysis and CAPA investigations. 
  • Excellent communication skills, capable of influencing stakeholders at all levels and leading cross-functional initiatives. 
  • Ability to thrive in a fast-paced environment and navigate ambiguity with sound judgment. 

Preferred qualifications 

  • Experience mentoring or leading junior engineers in design assurance or software/systems engineering activities. 
  • Experience with Capital Equipment
  • Knowledge of software quality standards (IEC 62304) and software/system development principles. 
  • Prior experience working on or supporting cardiac mapping systems or similar complex medical device platforms. 
  • Strong project management skills and familiarity with agile development methodologies. 

A propos du poste :

Nous offrons une opportunite a fort impact pour un(e) professionnel(le) senior en qualite de conception afin de diriger les activites d'assurance qualite de conception pour un dispositif medical critique dans le domaine de l'electrophysiologie. Ce role necessite une personne autonome capable de gerer de facon independante des defis techniques complexes et de developper des solutions couvrant les domaines materiel, logiciel et systeme. A ce titre, vous influencerez les initiatives strategiques en qualite, encadrerez des ingenieurs juniors et agirez comme ressource cle aupres d'equipes interfonctionnelles afin d'assurer la securite des produits, la conformite reglementaire et la robustesse de conception.

Mode de travail :

Chez Boston Scientific, nous valorisons la collaboration et la synergie. Ce poste hybride est base a Montreal, Canada, et requiert une presence sur site d'au moins trois (3) jours par semaine.

Parrainage de visa :

Boston Scientific n'offrira pas, a ce stade, de parrainage ni ne prendra en charge le parrainage d'un visa de travail pour ce poste.

Vos responsabilites comprendront :

  • Agir a titre d'autorite technique au sein de la qualite pour l'integration systeme, les decisions de conception, la gestion des risques ainsi que le developpement et la validation des logiciels.
  • Diriger de facon autonome les activites de controle de conception pour les equipements, incluant la planification de la conception et du developpement, la gestion des risques, la verification et la validation de conception, avec un fort accent sur la robustesse de la conception et de la documentation systeme.
  • Collaborer etroitement avec les equipes R&D, reglementaires, de fabrication et cliniques afin de fournir des conseils d'expert sur les aspects de conception et de conformite tout au long du cycle de vie du produit.
  • Assurer la gestion et le maintien des dossiers complets de gestion des risques (analyses des dangers, AMDE/FMEA), en couvrant le materiel, les logiciels et les systemes, et en appliquant des strategies avancees d'attenuation des risques pour orienter les decisions de conception.
  • Diriger les enquetes sur les causes fondamentales et la resolution des defaillances de tests, CAPA, NCEP et plaintes, en pilotant les actions correctives et preventives avec un minimum de supervision.
  • Offrir du mentorat et du soutien aux ingenieurs juniors en matiere de meilleures pratiques d'assurance qualite de conception, d'exigences reglementaires et de processus qualite.
  • Identifier de maniere proactive les lacunes et les opportunites d'amelioration continue des processus, outils et documents de developpement de produits.
  • Agir comme principal point de contact pour l'assurance qualite de conception lors des audits internes, externes et inspections reglementaires.
  • Gerer efficacement plusieurs priorites et projets de facon autonome, faire preuve d'un solide jugement en contexte d'ambiguite et influencer les equipes projet vers des decisions et comportements axes sur la qualite.

Qualifications requises :

  • Baccalaureat en genie mecanique, electrique, logiciel, biomedical ou dans une discipline technique connexe.
  • 7+ annees d'experience en assurance qualite, qualite de conception, qualite logicielle ou roles connexes dans l'industrie des dispositifs medicaux.
  • Expertise demontree en controles de conception, gestion des risques (ISO 14971), reglementation des systemes qualite (21 CFR 820) et systemes de gestion de la qualite (ISO 13485).
  • Capacite eprouvee a diriger de facon autonome des projets complexes de developpement de produits, incluant des activites qualite pour les logiciels et les systemes, de la conception a la realisation.
  • Experience dans l'elaboration et le maintien de la documentation des risques (AMDE/FMEA, analyses des dangers) avec une portee couvrant le materiel, les logiciels et les systemes.
  • Solides competences en resolution de problemes, incluant la direction d'analyses des causes fondamentales et d'enquetes CAPA.
  • Excellentes habiletes de communication, avec la capacite d'influencer des parties prenantes a tous les niveaux et de diriger des initiatives interfonctionnelles.
  • Capacite a evoluer dans un environnement dynamique et a naviguer dans l'ambiguite avec un jugement eclaire.

Qualifications souhaitees :

  • Experience en mentorat ou en encadrement d'ingenieurs juniors dans des activites d'assurance qualite de conception ou d'ingenierie logicielle/systemes.
  • Experience avec des equipements capitaux.
  • Connaissance des normes de qualite logicielle (IEC 62304) et des principes de developpement logiciel/systeme.
  • Experience prealable sur des systemes de cartographie cardiaque ou des plateformes de dispositifs medicaux complexes similaires.
  • Solides competences en gestion de projet et familiarite avec les methodologies de developpement agiles.

Requisition ID: 629670

Minimum Salary: $83,300

Maximum Salary: $132,300

The anticipated compensation and the value of core and optional employee benefits offered by Boston Scientific (BSC) - see www.bscbenefitsconnect.com--will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, among other relevant business or organizational needs. 

Compensation for hourly, non-sales roles may also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements). 

Compensation for salaried, non-sales roles may also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements). 

Compensation for sales roles is governed by Sales Incentive Compensation Plan (which includes certain annual non-discretionary incentives based on predetermined objectives). 

Our organization is across Canada and has commercial representation in 140 countries. 

This job involves regular collaboration with colleagues, clients, and stakeholders across Canada, the U.S., and/or internationally, making proficiency in English essential for effective communication and alignment. English is necessary for engaging with a range of documentation and maintaining effective communication if interacting with external clients or vendors. 

As detailed in the job description, this job involves communicating, both verbally and in writing, with other Boston Scientific teams located across Canada, the United States and/or with our international clients and partners. International customers and partners represent an important part of our activities. Based on an evaluation, we have determined that the duties of Senior Design Quality Engineer / Ingenieur principal en qualite de la conception position require knowledge of English in addition to French (oral and written). We also determined that the English language skills already required of other employees do not permit the performance of English language skills tasks related to Senior Design Quality Engineer / Ingenieur principal en qualite de la conception position. 

However, in Quebec, Boston Scientific limits as much as possible the number of positions for which it requires the knowledge of another language than French. Boston Scientific solely requires proficiency in English where it is necessary for the performance of an employee's duties. 

Boston Scientific transforms lives through innovative medical technologies that improve the health of patients around the world. As a global medical technology leader for more than 45 years, we advance science for life by providing a broad range of high-performance solutions that address unmet patient needs and reduce the cost of healthcare. Our portfolio of devices and therapies helps physicians diagnose and treat complex cardiovascular, respiratory, digestive, oncological, neurological and urological diseases and conditions. Learn more atwww.bostonscientific.comand follow us onLinkedIn. 

...

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About Boston Scientific

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As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen.

Industry

Medical equipment and supplies manufacturing, manufacturing and construction

Company size

10,000+ Employees

Headquarters location

Marlborough, MA, US

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