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Senior Physiotherapy Equipment Calibration Specialist

Hiring from
United Arab Emirates
Work type
Remote
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Job Title: Senior Physiotherapy Equipment Calibration Specialist

Location: United Arab Emirates (Remote)

Employment Type: Full-Time

Work Arrangement: 100% Remote — Work From Home

Level: Senior

About the Role

We are seeking an experienced Senior Physiotherapy Equipment Calibration Specialist to provide remote technical oversight, calibration documentation review, equipment performance analysis, and quality assurance support for physiotherapy and rehabilitation equipment. The role focuses on evaluating calibration records, reviewing technical specifications, monitoring equipment performance trends, and coordinating maintenance and calibration activities with healthcare facilities and authorized service providers.

This position is entirely remote and does not involve physically testing, calibrating, repairing, installing, or maintaining equipment. All hands-on technical activities must be performed by qualified local biomedical engineers, calibration technicians, or authorized service providers.

Key Responsibilities
  • Review calibration certificates, equipment performance records, and technical service reports for physiotherapy and rehabilitation devices.
  • Assess calibration documentation for completeness, accuracy, traceability, and alignment with applicable technical requirements.
  • Provide remote technical guidance on calibration schedules, equipment verification procedures, and quality documentation.
  • Review performance data for equipment such as electrotherapy units, ultrasound therapy devices, traction systems, exercise machines, and rehabilitation assessment equipment.
  • Evaluate calibration results against manufacturer specifications and approved acceptance criteria.
  • Analyze measurement deviations, recurring equipment failures, and calibration trends.
  • Review measurement uncertainty statements, reference standards, calibration intervals, and traceability records.
  • Coordinate calibration schedules and service documentation with healthcare facilities and authorized technical providers.
  • Monitor equipment maintenance histories and identify overdue calibration or verification requirements.
  • Review equipment qualification and performance verification documentation.
  • Support investigations into calibration failures, out-of-tolerance results, and equipment performance complaints.
  • Recommend corrective and preventive actions based on technical evidence and documented findings.
  • Maintain digital equipment registers, calibration histories, service records, and quality documentation.
  • Develop and improve calibration review checklists, technical procedures, and equipment monitoring reports.
  • Support internal audits and quality management reviews involving rehabilitation equipment.
  • Monitor relevant manufacturer guidance, technical standards, and applicable healthcare equipment quality requirements.
  • Prepare periodic reports on calibration compliance, equipment reliability, outstanding actions, and service performance.
  • Coordinate with clinical engineering, physiotherapy, procurement, quality assurance, and equipment maintenance teams.
Qualifications and Experience
  • Bachelor's degree in Biomedical Engineering, Clinical Engineering, Electrical Engineering, Instrumentation, or a related technical discipline.
  • Typically 5–8 years of experience in biomedical equipment calibration, clinical engineering, medical device quality assurance, or technical service management.
  • Experience with physiotherapy, rehabilitation, electrotherapy, and physical medicine equipment.
  • Strong understanding of calibration principles, measurement traceability, equipment verification, and measurement uncertainty.
  • Familiarity with calibration certificates, reference standards, equipment specifications, and acceptance criteria.
  • Knowledge of quality management systems and relevant medical device standards, such as ISO 13485 and ISO/IEC 17025.
  • Experience reviewing technical service reports, equipment maintenance records, and calibration documentation.
  • Ability to interpret technical manuals, equipment specifications, measurement results, and performance data.
  • Strong analytical and problem-solving skills, particularly in investigating calibration deviations and recurring equipment issues.
  • Familiarity with computerized maintenance management systems and digital equipment asset registers.
  • Excellent technical writing, documentation control, and reporting skills.
  • Strong communication and coordination skills when working with healthcare facilities and external service providers.
  • Ability to work independently and manage multiple equipment documentation and review activities in a fully remote environment.
What We Offer
  • A fully remote, work-from-home position based in the UAE.
  • Competitive compensation aligned with technical experience and qualifications.
  • Opportunities to support healthcare equipment quality and rehabilitation service reliability.
  • Collaboration with biomedical engineering, clinical engineering, and healthcare quality professionals.
  • Professional development in medical equipment standards, calibration governance, and quality assurance.
How to Apply

Interested candidates should submit an updated CV highlighting their experience in biomedical equipment calibration, physiotherapy equipment, technical documentation review, and medical device quality assurance.

Application Subject: Application – Senior Physiotherapy Equipment Calibration Specialist (UAE Remote)

Candidates should confirm applicable employment arrangements, residency requirements, and work authorization before accepting an offer.

  • Role Scope: This is a fully remote technical oversight and documentation role. Physical equipment testing, calibration, electrical safety testing, repairs, maintenance, installation, and on-site inspections must be performed by qualified local biomedical engineers or authorized service providers. Clinical decisions, equipment suitability determinations affecting patient treatment, and formal device release or regulatory approvals must remain with appropriately qualified and authorized professionals.

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