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Biomedical Technology jobs in Montréal, QC

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    • Reporting to the Senior Director, Biomedical Innovation this member of the Biomedical Innovation team is responsible for the product development process from…
    • Être membre de l’Association des technologues en génie biomédical (ATGBM) un atout.
    • Chaque jour, nous contribuons ensemble à sauver des vies.
    • Une entreprise chef de file spécialisée dans la conception d'équipements de mesure et de diagnostic haute précision souhaite ajouter un Technicien en réparation…
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    • Involvement in pedagogical days organized by the College.
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    • Working in conjunction with the Director of Academic Research, convert and present new and novel biometrical trial technologies, processes and findings into…
    • Participer à la conception et au développement de dispositifs médicaux tout en suivant un système qualité conforme à la norme ISO 13485.
    • Status: Full time permanent (40 h/week).
    • Reporting to the Senior Quality Manager, this member of the Quality team will provide direct supervision of the Quality…
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    • Prendre part aux journées pédagogiques organisées par le Collège;
    • Participate in the evaluation and implementation of new technologies.
    • The Medical Equipment and Systems Specialist is responsible for the coordination,…
    • Prendre en charge l’évaluation et l’intégration des composants, logiciels ou technologies attribués aux fournisseurs, tiers ou développés en externe.
    • Lead evaluation and system-level integration of supplier components, third-party technologies, externally developed software, or externally developed subsystems…
    • The candidate will contribute to progress science & technology as well as practical applications in the field of life sciences research and clinical application…
    • The role serves as a technical liaison between Manufacturing, Quality, and Engineering, helping to maintain process control, support technology transfer…
    • Soutenir et améliorer les processus qualité conformément aux exigences ISO 13485, MDSAP, EU MDR, FDA 21 CFR Part 820 et Canadian Medical Devices Regulations (…
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Product Development Specialist III
Montréal, QC
Permanent, Full-time

Job details

Here’s how the job details align with your profile.

Job type

Permanent
Full-time

Full job description

Job Overview
Reporting to the Senior Director, Biomedical Innovation this member of the Biomedical Innovation team is responsible for the product development process from concept to final design review of mechanical components in existing and new Agile MV Technologies Inc (A Resonetics Company) products. Ensuring the smooth running of all operations activities in line with ISO 13485, FDA, GMPs, CE mark such as the following tasks.

Responsibilities

  • Participate in the design and development of medical devices while following a quality system in accordance with ISO 13485.
  • Prepare engineering 3D models drawings of products and prototypes.
  • Produce and maintain design files in a regulatory framework.
  • Participate in risk management and audit.
  • Develop and manage design verification and validation activities.
  • Manage the transfer of products from design to manufacturing.
  • Work with Agile MV customers to identify their needs and provide a consulting role throughout the life cycle of medical devices.
  • Prepare test reports by collecting, analyzing and summarizing information.
  • Train and support technicians during manufacturing-related activities
  • Collaborate with internal departments of Agile MV, such as quality and manufacturing departments to ensure the development of medical devices.
  • Take responsibility in the team and in the project.
  • Supervise the work of a multidisciplinary team, plans the work, establishes performance.
  • May carry out projects from A to Z with the support of the manager.
  • To maximize the effectiveness of the position, this job description is subject to change according to a consensus of the 2 parties (Agile MV Technologies Inc «A Resonetics Company» and the employee).

Qualifications

- Graduated with a bachelor’s degree in engineering, Physical Sciences or an equivalent

- Minimum of 5 Years of experience in a similar position in the industry.

- Experience in risk management.

- Knowledge of quality and conformity systems.

- Experience in 3D modelling with SolidWorks software.

- Strong analytical skills, solutions focus in an autonomous manner.

- Advanced level of English and French, spoken and written.

- A strong team player able to contribute to discussions.

- Detail oriented, quality focused, meticulous, and versatile individual.

- Adaptable, hardworking, and able to work under pressure.

- Advanced level of oral and written French.

- Advanced level of English, to interact with customers and suppliers who are mainly international. To comply with international industry standards.

Job Types: Full-time, Permanent

Work Location: In person

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