We are seeking a hands-on Senior Full Stack .NET Developer to join an enterprise technology team responsible for building, integrating, and supporting business-critical applications and collaboration platforms. The successful candidate will work closely with senior engineers, product owners, and business stakeholders to design and deliver scalable, secure, and maintainable software solutions across both front-end and back-end technologies.
Main Responsibilities
About the Role
We are seeking an experienced Medical Device Design Documentation Engineer to support post-market activities for existing Design History Files (DHFs) within a regulated medical device environment. Reporting to a Project Leader or Manager, you will contribute to the maintenance, update, and execution of DHF documentation while collaborating closely with Regulatory, Quality, and Engineering teams. This role requires strong technical writing skills, attention to deta...
About the Role
We are seeking an experienced Medical Device Design Documentation Engineer to support post-market activities for existing Design History Files (DHFs) within a regulated medical device environment. Reporting to a Project Leader or Manager, you will contribute to the maintenance, update, and execution of DHF documentation while collaborating closely with Regulatory, Quality, and Engineering teams. This role requires strong technical writing skills, attention to deta...
IAM / Okta Analyst – Authorization POC
Location: Remote across Canada — preference for candidates in Quebec
Experience: Senior / hands-on IAM & Okta experience
Duration: Until the end of the year, with potential renewal for several years
Hours: 35 hours/week
About the Role
Our client is a leading insurance organization currently modernizing and expanding its Identity & Acces...
IAM / Okta Analyst – Authorization POC
Location: Remote across Canada — preference for candidates in Quebec
Experience: Senior / hands-on IAM & Okta experience
Duration: Until the end of the year, with potential renewal for several years
Hours: 35 hours/week
About the Role
Our client is a leading insurance organization currently modernizing and expanding its Identity & Acces...
About the Role
We are seeking an experienced Medical Device Design Documentation Engineer to support post-market activities for existing Design History Files (DHFs) within a regulated medical device environment. Reporting to a Project Leader or Manager, you will contribute to the maintenance, update, and execution of DHF documentation while collaborating closely with Regulatory, Quality, and Engineering teams. This role requires strong technical writing skills, attention to deta...