Device Integration engineer for medical domain

Job Requirements

Job Title: Device Integration engineer for medical domain

At Quest Global, it's not just what we do but how and why we do it that makes us different. With over 25 years as an engineering services provider, we believe in the power of doing things differently to make the impossible possible. Our people are driven by the desire to make the world a better place—to make a positive difference that contributes to a brighter future. We bring together technologies and industries, alongside the contributions of diverse individuals who are empowered by an intentional workplace culture, to solve problems better and faster.

Role Overview

We are seeking a Device Integration Engineer to lead the integration and validation of radiation dose monitoring systems. The role will be responsible to validate system integrations, validate workflows building automation to scale validation processes and compliance reporting.

Key Responsibilities

• System Integration & Deployment

• Integrate with new modality devices, PACS, RIS/EMR, using DICOM (RDSR, MPPS), HL7 and other relevant interoperability standards.

• Lead end-to-end integration into dose monitoring platforms

• Device data validation & normalization

• Validate dose parameters such as CTDIvol, DLP, kVp/mAs, and effective dose (mGy/mSv) for accuracy and normalization.

• Ensure correct parsing and mapping of RDSRs into dose management system database
• Implement and maintain dose conversion models such as ICRP 103, organ dose estimation.
• Map scan regions to conversion coefficients based on patient demographics and modality.
• Validate effective dose calculations for consistency across devices and protocols.

• Data Quality & Automation

• Develop automated validation scripts for ingestion and conversion accuracy.

• Troubleshoot anomalies in dose reporting and escalate clinical concerns.

• Regulatory & Reporting Compliance

• Ensure compliance with ACR DIR, Joint Commission, Euratom, and other frameworks.

• Generate reports for audits, external submissions, and performance benchmarking.
• Maintain PHI security and privacy in on-prem and cloud environments.

• Training & Documentation

• Train L1-L3 services, commercial and engineering on system usage and dose interpretation.

• Document system configurations, conversion logic, and validation protocols.

Skills & Qualifications

Technical Skills

• Strong knowledge of DICOM, HL7, and imaging informatics workflows.
• Proficiency in Python, SQL, or similar for data transformation and validation.
• Experience with dose management platforms (DoseWatch, Radimetrics, DoseTrack).
• Familiarity with cloud platforms (Azure, AWS) and secure data handling.

Clinical & Analytical Skills

• Deep understanding of radiation dose metrics (CTDIvol, DLP, air kerma) and conversion methodologies.
• Ability to interpret clinical dose data and collaborate with medical physicists.
• Knowledge of ALARA, DRLs, and regulatory standards.

Soft Skills

• Excellent communication and cross-functional collaboration.
• Strong problem-solving and analytical mindset.
• Project management experience in multi-site healthcare deployments.

Preferred Qualifications

• Bachelor's or Master's in Biomedical Engineering, Health Informatics, Medical Physics, or related field.
• Certification in Imaging Informatics (CIIP) or equivalent.
• Experience in hospital or radiology environments.

Work Experience

Mandatory Skills: DICOM, HL7, Experience with scripting (e.g., Python, SQL), Medical Device Integration/validation in different modalities

Nice to have skills:

Certification in Imaging Informatics (CIIP) or equivalent.

Ability to interpret clinical dose data and collaborate with medical physicists.

Knowledge of ALARA, DRLs, and regulatory standards.

Experience in hospital or radiology environments.

Familiarity with cloud platforms (Azure, AWS), Deep understanding of radiation dose metrics (CTDIvol, DLP, air kerma) and conversion methodologies