Remote Medical Device Software Assessor (Contractor)

Jobgether; Saudi Arabia; Remote; SAR 180,000 - 240,000; Full time

Benefits offered by this job

Fully remote contractor position.

Flexible scheduling

Exposure to international regulatory

Work on AI-enabled medical device tech

Job summary

Jobgether is seeking a Product Reviewer – Contractor based in Saudi Arabia to independently assess medical device software documentation and lifecycle processes, including SaMD and AI-enabled devices. You will evaluate compliance with EU MDR, UK MDR, and relevant IEC standards, and communicate findings to manufacturers.

The role offers fully remote work with flexible scheduling, international regulatory exposure, and the opportunity to contribute to advancing medical device safety and

Qualifications

• Bachelor's degree or higher in a software-related field.
• 4+ years in medical device or safety-critical sector.
• 2+ years designing, developing, or testing safety-critical software.
• Experience as Product Reviewer or technical documentation assessor for a notified/UK body.

Responsibilities

• Assess manufacturers' software lifecycle processes and technical documentation for medical device software (SaMD and AI-enabled devices).
• Evaluate compliance with EU MDR, UK MDR, IEC 62304, IEC 82304-1, IEC 62366-1, IEC 81001-5-1.

Skills

Regulatory assessment

Technical writing

Independent judgment

Communication skills

Software lifecycle knowledge

Auditing experience

Education

Bachelor's degree in Software Engineering

Bachelor's degree in Computer Science / Electrical or Electronic Engineering

Job description

Jobgether is seeking a Product Reviewer – Contractor based in Saudi Arabia to independently assess medical device software documentation and lifecycle processes, including SaMD and AI-enabled devices. You will evaluate compliance with EU MDR, UK MDR, and relevant IEC standards, and communicate findings to manufacturers.

The role offers fully remote work with flexible scheduling, international regulatory exposure, and the opportunity to contribute to advancing medical device safety and