Innovative Health

The Regulatory Affairs Specialist role is responsible for preparing and submitting the appropriate documentation for FDA 510(k) submissions and documentation for other international regulatory bodies.Responsible for managing and preparing 510(k) submissions to obtain FDA clearance to

The Regulatory Affairs Specialist role is responsible for preparing and submitting the appropriate documentation for FDA 510(k) submissions and documentation for other international regulatory bodies.Responsible for managing and preparing 510(k) submissions to obtain FDA clearance to

The Regulatory Affairs Specialist role is responsible for preparing and submitting the appropriate documentation for FDA 510(k) submissions and documentation for other international regulatory bodies.Responsible for managing and preparing 510(k) submissions to obtain FDA clearance to

The Regulatory Affairs Specialist role is responsible for preparing and submitting the appropriate documentation for FDA 510(k) submissions and documentation for other international regulatory bodies.Responsible for managing and preparing 510(k) submissions to obtain FDA clearance to

The Manufacturing Technician is responsible for supporting the Manufacturing Engineer in sustaining production and implementing process improvements. Assists production by ensuring facilities equipment tooling fixtures materials and documentation meet production and quality requiremen

The Manufacturing Technician is responsible for supporting the Manufacturing Engineer in sustaining production and implementing process improvements. Assists production by ensuring facilities equipment tooling fixtures materials and documentation meet production and quality requiremen

The Quality Engineer will ensure compliance to required standards including FDA and ISO during process development and the manufacturing of medical device addition this person will have responsibility for identifying and driving improvements related to quality compliance to regulator

The Quality Engineer will ensure compliance to required standards including FDA and ISO during process development and the manufacturing of medical device addition this person will have responsibility for identifying and driving improvements related to quality compliance to regulator

The Regulatory Affairs Associate role is responsible for assisting with preparing and submitting the appropriate documentation for pre-market submissions (i.e. FDA 510(k) submissions Health Canada Device License Applications). This role also supports post-market regulatory compliance

The Regulatory Affairs Associate role is responsible for assisting with preparing and submitting the appropriate documentation for pre-market submissions (i.e. FDA 510(k) submissions Health Canada Device License Applications). This role also supports post-market regulatory compliance

The Regulatory Affairs Engineer role is responsible for preparing and submitting the appropriate documentation for FDA 510(k) submissions and documentation for other international regulatory bodies.Responsible for managing and preparing 510(k) submissions to obtain FDA clearance to co

The Regulatory Affairs Engineer role is responsible for preparing and submitting the appropriate documentation for FDA 510(k) submissions and documentation for other international regulatory bodies.Responsible for managing and preparing 510(k) submissions to obtain FDA clearance to co

Position Summary:Provides technical support to manufacturing and related functions. Researches develops and improves manufacturing processes methods and systems for products facilities fixtures tooling equipment and/or materials. Develops and tests work methods and procedures ensuring

Position Summary:Provides technical support to manufacturing and related functions. Researches develops and improves manufacturing processes methods and systems for products facilities fixtures tooling equipment and/or materials. Develops and tests work methods and procedures ensuring