Posted 2 days ago
The Quality Systems Engineer III supports global quality system processes and digital document and records control platforms, ensuring regulatory compliance, audit readiness, and effective system performance. Responsibilities include IT partnership, process improvement, CAPA and risk activities, audit support, global projects, and training and mentoring colleagues.
Posted 3 days ago
The R&D Systems III translates user needs into system and subsystem design requirements, manages specifications and traceability, and supports product development across its lifecycle. Responsibilities include systems verification and validation, testing, risk documentation, design change assessments, regulatory submissions, and collaboration with cross-functional teams in a medical device environment.
Posted 3 days ago
The Clinical Specialist III provides expert clinical and product support for Boston Scientific electrophysiology products, supporting customer adoption across hospitals and working closely with clinicians, territory managers, and sales and marketing teams. Responsibilities include training, demonstrations, troubleshooting, clinical research support, territory and customer relationship management, and travel to provide product support.
Posted 3 days ago
The Supply Chain Associate, Co-op/New Grad supports the Supply Chain department with systems, processes, reporting, and operational and administrative tasks across purchasing, planning, and logistics. Responsibilities include inventory analysis, purchase order and supplier follow-up, inventory and material planning, master data audits, shipment updates, customs paperwork, and process improvement.
Posted 3 days ago
The R&D Systems Intern collaborates with the R&D Engineering team to design and evaluate medical devices, conduct feasibility studies, and develop concepts through market release. Responsibilities include coordinating project activities, maintaining R&D documentation, improving processes using Agile and Lean principles, and contributing to software and system risk assessment and Design FMEA activities.
Posted 3 days ago
The Process Engineering Associate supports the design, development, and optimization of manufacturing processes and equipment, including prototyping, testing, validation, and process characterization. The role also contributes to Lean improvements, technical documentation, safety, and compliance with ISO 13485 and FDA requirements in a medical technology manufacturing environment.
Posted 3 days ago
The Marketing & Biomedical Communications Associate is an eight-month placement supporting the Biomedical Communications team in creating clinically accurate promotional, educational, and marketing content for medical devices. Responsibilities include researching products and clinical workflows, developing communications materials, coordinating with cross-functional stakeholders to meet regulatory and business requirements, and following company policies.
Posted 3 days ago
The Senior Design Quality Engineer leads design assurance for a critical electrophysiology medical device, overseeing design controls, risk management, verification and validation, and product compliance across hardware, software, and system domains. The role also leads investigations and corrective actions, supports audits, mentors junior engineers, and collaborates with cross-functional teams to strengthen product safety and design quality.
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