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Medical Device jobs in Montréal, QC

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    • Participate in the design and development of medical devices while following a quality system in accordance with ISO 13485.
    • Job Types: Full-time, Permanent.
    • Participer à la conception et au développement de dispositifs médicaux tout en suivant un système qualité conforme à la norme ISO 13485.
    • Se joindre à Puzzle Medical, c’est faire partie d’une équipe engagée à améliorer le traitement de l’insuffisance cardiaque avancée.
    • Options d'Achats d'Actions.
    • Experience in the medical or pharmaceutical field industry is an asset.
    • Status: Full time permanent (40 h/week).
    • Maintain a clean and orderly workstation.
    • The QA Inspector is responsible for inspecting incoming materials, inspecting and testing Final medical devices.
    • Determine the appropriate sample size.
    • The Senior Specialist, Quality, Team Lead at Agile MV Technologies Inc (a Resonetics company) will be responsible for supporting company quality and regulatory…
    • A Clinical Lab Technician, Microbiologist or Analytical Chemist / Biochemist with extensive experience on running clinical analytical assays on various clinical…
    • As a Bilingual Customer Service Engineer for Reynolds and Reynolds, you will perform onsite installation and maintenance support on a variety of computer…
    • Assist passengers with personal belongings, medical devices, and sensitive items.
    • Paid training and ongoing development opportunities.
    • View all GardaWorld Security Screening Inc. jobs - Dorval jobs
    • Salary Search: Facilitator salaries
    • See popular questions & answers about GardaWorld Security Screening Inc.
    • Implementing the technique, carrying out the adjustments and calibration of the device and applying inspection procedures, according to one’s certifications.
    • Our team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials.
    • Benefits eligibility starts on your first day of hire and comprises of 100% company paid medical, dental, and vision coverage, including a Health Spending…
    • The Medical Equipment and Systems Specialist is responsible for the coordination, verification and/or maintenance of equipment and related system installations.
    • Recognized leadership in the field of medical devices.
    • The Director General of MDRC will inspire and lead Bioengineering Technologies R&D focused on advancing…
    • Experience in the field of medical devices or related research and development.
    • Project experience in medical devices or a research-and-development environment.
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Product Development Specialist III
Montréal, QC
Permanent, Full-time

Job details

Pay information not provided
Permanent, Full-time
Montréal, QC

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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