Aegis Ventures

Analyst

• Perform manual visual review of medical imaging studies using approved DICOM viewers
• Validate imaging studies against client-specific acceptance criteria, including:
• Modality and series accuracy
• Anatomical coverage and completeness
• Image usability and acquisition artifacts
• Confirm required images and series are present and properly structured
• Verify that no Protected Health Information (PHI) is present in imaging data prior to delivery, including:
• Burned-in text or annotations
• Overlays and image corners
• Confirm imaging data has been properly de-identified according to Avandra standards
• Identify, flag, and escalate suspected PHI exposure or de-identification failures
• Document review outcomes using Avandra QA workflows and tools
• Apply standardized pass, fail, or needs-review determinations
• Maintain clear, auditable records of quality and privacy reviews
• Participate in calibration and training sessions to maintain review consistency
• Provide feedback to improve automated quality and de-identification checks
• Collaborate with Imaging Operations and Engineering teams as needed

Imaging Quality Analyst – Part-Time

Systems Engineer

• Diagnose and resolve software, system, and infrastructure issues across Avandra’s products and internal tooling
• Act as a technical point of contact for escalated or ambiguous issues impacting reliability, performance, or accessibility
• Support deployment, configuration, and maintenance of software, hardware, and internal systems
• Contribute to the quality and reliability of Avandra’s software through structured QA processes
• Write and maintain automated test suites (integration, regression, smoke tests)
• Participate in release testing and validation efforts
• Ensure appropriate test coverage for new features and critical infrastructure
• Write scripts and tools for deployment, monitoring, and troubleshooting
• Support infrastructure provisioning and configuration using automation tools (e.g., Terraform, Ansible)
• Improve system observability through logging, alerting, and dashboards
• Identify repetitive tasks and build automated solutions to reduce manual effort

System Engineer – Part-Time

QA Engineer

• Support regulatory strategy and submission timelines for US market
• Support management of medical device listing, establishment registration, and labeling compliance
• Own quality oversight of supplier relationships for US market
• Conduct supplier audits (remote and on-site) and manage audit findings to closure
• Lead CAPA investigations and effectiveness verification
• Manage incoming inspection criteria and supplier performance metrics
• Coordinate design transfer and manufacturing scale-up activities
• Maintain design control documentation (DHF) for hardware products
• Handle complaint investigations and MDR reporting
• Support document control and training record maintenance
• Partner with Engineering on design verification/validation protocols
• Work with Operations on manufacturing quality requirements
• Coordinate with Director of QA/RA on global compliance strategy

Senior QA/RA Specialist

Clinical Research

• Support site start-up activities, including creation of study templates, CRFs, study manuals, site shipments, investigator binders and investigational device accountability.
• Support data entry, query tracking, and remote and on-site monitoring needs in collaboration with CRO and internal team members.
• Support or lead IRB submissions.
• Maintain essential documents in the Trial Master File (TMF) per regulatory and company standards.
• Coordinate clinical trial logistics such as meeting scheduling, site communications, and shipping of study materials.
• Collaborate with CRO, central reading centers and other vendors as needed.
• Draft and distribute study-related communications, agendas, and minutes.
• Ensure adherence to GCP, ISO 14155, and regulatory guidelines with supervision.
• Assist in the preparation of clinical study reports, presentations, and regulatory submissions.
• Contribute to the development of SOPs, templates, and internal workflows.

Imaging Quality Analyst – Part-Time

System Engineer – Part-Time

Senior QA/RA Specialist

Clinical Trial Specialist