Industrial Jobs

Product Compliance Specialist

We are seeking an experienced Product Surveillance/Complaint Specialist. Working under general supervision, the Specialist receives, reviews, evaluates, investigates, and resolves medical device complaints. Maintains quality documents to ensure compliance with various regulatory agencies. Analyzes complaint data and trends. Coordinates the resolution of complaints and ensures that timely investigations are performed. Provides feedback to the development, manufacturing, and quality teams on potential product improvements for medical products. Prepares and files Medical Device Reports as appropriate to the U. S. Food & Drug Administration (FDA) and Health Canada (HC). Generates customer letters upon completion of investigation as appropriate.

Preventive Maintenance Coordinator

The team will review equipment on a schedule that ensures PM strategies are established in alignment with the Operating Cycle Plan schedule. After receiving Bruce A & B Preventive Maintenance Oversight Group approval to activate proposed PMIDs, the Team Lead will ensure that the endorsed PMIDs are assigned to the relevant Station assessing groups for processing and scheduling using the established processes.

Senior Electrical Engineer

Lead the design, development and testing of medical electronic systems for neurosurgical systems
Develop system level technical specifications and support creation of verification and validation plans
Produce design documentation including specifications, schematics, PCB, layouts, test protocols, BOM, manufacturing instructions
Experience with electrical design and related tools such as Altium and other electronic design tools.

Quality Systems Engineer

Quality Engineering at Synaptive Medical is an integrated function in product development teams. Each Quality Engineer acts as a counter-part to the Systems Engineer on one or more products, providing insight from Quality and Regulatory perspectives. QEs have the opportunity to participate in discussions and activities throughout the lifecycle of the product, from Ideation to Production. Unlike Quality Engineering role in manufacturing sector, this role requires sound knowledge of design, development and medical device standards. Synaptive is looking for a QE to join an integrated opto-electromechanical team.

Legacy Registration – Technical Advisor

Provide engineering support for registration of all pressure retaining systems, components and structures to meet Bruce A and Bruce B Licensing requirements.


Prepare Estimates & Supporting Bidding Processes for large, complex, multi discipline, design-build, vertical construction projects.

DT/RT Systems Engineering Lead

Review vendor documentation including Design Requirements, Requirement Traceability matrices, Failure Modes and Effects Analyses, and System level tooling documentation from a Systems point of view


As a member of the U3-8 MCR (Major component replacement) team you will be working within the Plant Design Engineering department (PDE) to support the Engineering oversight of the Detube/Retube tooling systems from the preliminary Engineering phase through to manufacture, testing and acceptance.

Conventional Maintanence FLM.

Lead a team responsible for the safe and effective execution of work coinciding with approved procedures by acting as a coach, facilitator and supervisor while creating and sustaining a cooperative/supportive team environment.

© 2018 Cronos Consulting Group