Synaptive Medical jobs

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Clinical Services & Implementation Specialist

Synaptive Medical - Canada
Lastly, they are passionate about Synaptive Medicals vision and with providing the best possible training experience to the customer....

Builds and Continuous Integration Developer

Synaptive Medical - Toronto, ON
You will collaborate with the various product, software development, test, and QA teams to support a performance culture by coordinating and managing the

Application Developer

Synaptive Medical - Toronto, ON
Joining the development team, this developer will have a focus on health monitoring, control system and network layers that aid in the safe, reliable production...

Scientific Developer - Distributed Computing

Synaptive Medical - Toronto, ON
Delivery of software in a regulated market (particularly medical devices). As a member of the Bridge team, you will be responsible for design, implementation,...

Intermediate Application Developer

Synaptive Medical - Toronto, ON
Synaptive Medical is looking for a person who enjoys solving technical problems within a fast-paced environment while following the quality development...

Informatics Specialist

Synaptive Medical - Canada
Knowledge of Diagnostic and Therapeutic Medical Imaging Modalities. Reporting directly to the Director(s) of Sales, the Informatics Specialist is responsible...

Facilities Manager

Synaptive Medical - Toronto, ON
The Facilities Manager is someone that is eager to lead or roll up their sleeves to get the job done. They are the hands-on type with a unique ability to

Quality Systems Associate

Synaptive Medical - Toronto, ON
Own the development and implementation of aspects of Synaptive Medical’s quality management system. Minimum 2 years experience in a medical device or...

Quality Systems Specialist - Audits

Synaptive Medical - Toronto, ON
Minimum 3 years experience leading or being a part of internal audits in a medical device or pharmaceutical company....

Regulatory Affairs Associate

Synaptive Medical - Toronto, ON
Minimum 1-2 years of medical device experience in a similar role. Familiarity with FDA’s medical device regulations, SOR/98-282, EU MDD, ISO standards, etc....

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