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Biomedical Scientist Jobs in Quebec (NOW HIRING)

DropGenie

Test Engineer - Microfluidics

Montreal, QC · On-site

Degree or diploma in Biomedical Engineering, Mechanical Engineering, Materials Science, Physics, or a related field * Hands-on experience with microfabrication or microfluidic device testing ...

Td

Applied Machine Learning Scientist II

Montreal, QC

CA$125K - CA$154K/yr

We're looking for a highly motivated Applied Machine Learning Scientist II to join our AI2 team. In this role, you'll apply expertise across the end-to-end AI and machine learning lifecycle ...

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All JobsBiomedical Scientist JobsBiomedical Scientist Jobs in Quebec

Biomedical Scientist information

See Quebec salary details

$15

$37

$63

How much do biomedical scientist jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for biomedical scientist in Quebec is $37.87, according to ZipRecruiter salary data. Most workers in this role earn between $25.48 and $49.04 per hour, depending on experience, location, and employer.

What is a biomedical scientist?

Biomedical scientist research new ways to diagnose, treat, and prevent disease using their knowledge of both biology and medicine. As a biomedical scientist, your responsibilities involve performing medical research, usually analyzing cultured cells or samples and conducting clinical trials to test prevention and treatment methods. Biomedical scientists work in laboratories at pharmaceutical companies, hospitals, and universities.

What is a biomedical scientist?

Biomedical scientists are professionals who conduct laboratory and scientific tests to help diagnose, treat, and prevent diseases. They analyze samples of blood, tissue, and other bodily fluids, providing critical data that supports patient care and medical research. Biomedical scientists often work in hospitals, research institutions, or public health laboratories, collaborating closely with doctors and other healthcare professionals. Their work is essential for identifying disease patterns, developing new treatments, and ensuring the safety and effectiveness of medical procedures.

What are some typical collaborative projects that a biomedical scientist might participate in within a hospital setting?

Biomedical Scientists often work closely with doctors, nurses, and other healthcare professionals to diagnose diseases and monitor patient health. In a hospital setting, they may participate in multi-disciplinary team meetings to discuss complex cases, contribute to research studies aimed at improving diagnostic techniques, or assist in the development of new laboratory protocols. Collaboration is essential for ensuring accurate results and integrating laboratory findings into patient care. This teamwork not only enhances patient outcomes but also provides valuable professional development opportunities.

What are the key skills and qualifications needed to thrive as a biomedical scientist, and why are they important?

To thrive as a Biomedical Scientist, you need a strong background in biological sciences, laboratory techniques, and a relevant degree such as biomedical science, often supplemented by professional registration or certification. Familiarity with laboratory information management systems (LIMS), advanced diagnostic equipment, and quality control protocols is critical. Attention to detail, analytical thinking, and effective teamwork are vital soft skills for ensuring accurate results and smooth laboratory operations. These competencies are essential for maintaining high standards in research and diagnostics, directly impacting patient care and scientific advancement.

What is the difference between Biomedical Scientist vs Medical Laboratory Technician?

AspectBiomedical ScientistMedical Laboratory Technician
Required CredentialsBachelor's degree in biomedical science or related field, often with registration or licensingDiploma or associate degree in medical laboratory technology, often with certification
Work EnvironmentHospitals, research labs, diagnostic laboratoriesClinical laboratories, hospitals, diagnostic centers
Employer & IndustryHealthcare, research, diagnosticsHealthcare, diagnostics, clinical testing
Common Search & ComparisonBiomedical Scientist vs Medical Laboratory Technician

Biomedical Scientists and Medical Laboratory Technicians both work in clinical labs and healthcare settings, but Biomedical Scientists typically hold higher qualifications and are involved in more complex testing and research. Medical Laboratory Technicians perform routine tests under supervision. Understanding these differences helps in choosing the right career path or job role.

Do biomedical scientists make good money?

Biomedical scientists typically earn a median annual salary that varies by country and experience level, with entry-level positions starting lower and experienced professionals earning higher wages. Salaries are influenced by factors such as education, certifications, and workplace setting, often including laboratories, hospitals, or research institutions. Overall, biomedical scientists can have a stable income, especially with advanced degrees and specialized skills.

What are the jobs for biomedical scientists?

Biomedical scientists work in laboratories conducting research, diagnostics, and testing to understand diseases and develop treatments. They may work in hospitals, research institutions, or pharmaceutical companies, often using techniques like microscopy, molecular biology, and data analysis. Roles include clinical scientist, research scientist, laboratory manager, and biomedical analyst, often requiring relevant certifications and laboratory skills.

What can you do as a biomedical scientist?

A biomedical scientist conducts laboratory research to understand diseases, develop treatments, and improve healthcare. They analyze biological samples, use specialized equipment, and often work in clinical or research settings, requiring knowledge of laboratory techniques and relevant certifications.

What jobs do you get with biomedical scientist?

A biomedical scientist can work in laboratories conducting research, diagnostics, and testing of biological samples. They may work in hospitals, research institutions, or pharmaceutical companies, often using tools like microscopes and laboratory equipment. Certification and knowledge of laboratory safety and procedures are typically required.
More about Biomedical Scientist jobs

What are popular job titles related to Biomedical Scientist jobs in Quebec?

For Biomedical Scientist jobs in Quebec, the most frequently searched job titles are:

What are popular job titles related to Biomedical Scientist jobs in QC?

For Biomedical Scientist jobs in QC, the most frequently searched job titles are:

Biomedical Scientist jobs near you
Infographic showing various Biomedical Scientist job openings in Quebec as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 73% Full Time, 13% Part Time, and 12% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $78,779 per year, or $37.9 per hour.

Senior Design Quality Engineer / Ingénieur principal en qualité de la conception

Boston Scientific

Montreal, QC • Hybrid

Full-time

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

32nd of 545 rated manufacturers

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.

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

Chez Boston Scientific, nous vous donnerons l’opportunité d’exploiter tout ce qui est en vous en travaillant dans des équipes d’employés diversifiés et hautement performants, pour relever certains des défis les plus importants de l’industrie de la santé. Grâce à l'accès aux derniers outils, informations et formations, nous vous aiderons à faire progresser vos compétences et votre carrière. Ici, vous serez accompagné 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. 

À propos du poste :

Nous offrons une opportunité à fort impact pour un(e) professionnel(le) senior en qualité de conception afin de diriger les activités d’assurance qualité de conception pour un dispositif médical critique dans le domaine de l’électrophysiologie. Ce rôle nécessite une personne autonome capable de gérer de façon indépendante des défis techniques complexes et de développer des solutions couvrant les domaines matériel, logiciel et système. À ce titre, vous influencerez les initiatives stratégiques en qualité, encadrerez des ingénieurs juniors et agirez comme ressource clé auprès d’équipes interfonctionnelles afin d’assurer la sécurité des produits, la conformité réglementaire et la robustesse de conception.

Mode de travail :

Chez Boston Scientific, nous valorisons la collaboration et la synergie. Ce poste hybride est basé à Montréal, Canada, et requiert une présence sur site d’au moins trois (3) jours par semaine.

Parrainage de visa :

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

Vos responsabilités comprendront :

  • Agir à titre d’autorité technique au sein de la qualité pour l’intégration système, les décisions de conception, la gestion des risques ainsi que le développement et la validation des logiciels.
  • Diriger de façon autonome les activités de contrôle de conception pour les équipements, incluant la planification de la conception et du développement, la gestion des risques, la vérification et la validation de conception, avec un fort accent sur la robustesse de la conception et de la documentation système.
  • Collaborer étroitement avec les équipes R&D, réglementaires, de fabrication et cliniques afin de fournir des conseils d’expert sur les aspects de conception et de conformité 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 matériel, les logiciels et les systèmes, et en appliquant des stratégies avancées d’atténuation des risques pour orienter les décisions de conception.
  • Diriger les enquêtes sur les causes fondamentales et la résolution des défaillances de tests, CAPA, NCEP et plaintes, en pilotant les actions correctives et préventives avec un minimum de supervision.
  • Offrir du mentorat et du soutien aux ingénieurs juniors en matière de meilleures pratiques d’assurance qualité de conception, d’exigences réglementaires et de processus qualité.
  • Identifier de manière proactive les lacunes et les opportunités d’amélioration continue des processus, outils et documents de développement de produits.
  • Agir comme principal point de contact pour l’assurance qualité de conception lors des audits internes, externes et inspections réglementaires.
  • Gérer efficacement plusieurs priorités et projets de façon autonome, faire preuve d’un solide jugement en contexte d’ambiguïté et influencer les équipes projet vers des décisions et comportements axés sur la qualité.

Qualifications requises :

  • Baccalauréat en génie mécanique, électrique, logiciel, biomédical ou dans une discipline technique connexe.
  • 7+ années d’expérience en assurance qualité, qualité de conception, qualité logicielle ou rôles connexes dans l’industrie des dispositifs médicaux.
  • Expertise démontrée en contrôles de conception, gestion des risques (ISO 14971), réglementation des systèmes qualité (21 CFR 820) et systèmes de gestion de la qualité (ISO 13485).
  • Capacité éprouvée à diriger de façon autonome des projets complexes de développement de produits, incluant des activités qualité pour les logiciels et les systèmes, de la conception à la réalisation.
  • Expérience dans l’élaboration et le maintien de la documentation des risques (AMDE/FMEA, analyses des dangers) avec une portée couvrant le matériel, les logiciels et les systèmes.
  • Solides compétences en résolution de problèmes, incluant la direction d’analyses des causes fondamentales et d’enquêtes CAPA.
  • Excellentes habiletés de communication, avec la capacité d’influencer des parties prenantes à tous les niveaux et de diriger des initiatives interfonctionnelles.
  • Capacité à évoluer dans un environnement dynamique et à naviguer dans l’ambiguïté avec un jugement éclairé.

Qualifications souhaitées :

  • Expérience en mentorat ou en encadrement d’ingénieurs juniors dans des activités d’assurance qualité de conception ou d’ingénierie logicielle/systèmes.
  • Expérience avec des équipements capitaux.
  • Connaissance des normes de qualité logicielle (IEC 62304) et des principes de développement logiciel/système.
  • Expérience préalable sur des systèmes de cartographie cardiaque ou des plateformes de dispositifs médicaux complexes similaires.
  • Solides compétences en gestion de projet et familiarité avec les méthodologies de développement 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 / Ingénieur principal en qualité 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 / Ingénieur principal en qualité de la conception position. 

However, in Québec, Boston Scientific limits as much as possible the number of positions for which it requires the knowledge of another language t

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About Boston Scientific

Sourced by ZipRecruiter

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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