Associate Quality Engineer
Core
Design, implement, and maintain quality assurance protocols for processing materials into finished medical devices, ensuring compliance with safety and regulatory standards.
Role type
Associate Quality Engineer
Builds
Medical device manufacturing processes and finished products
Domain
Medical technology / Musculoskeletal implants
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Quality inspection, regulatory compliance (FDA, ISO 13485), risk assessment, design verification and validation, report production, change management
Preferred skills
Analytical and problem-solving skills, attention to detail, organizational skills
Technologies
MS Office applications
Responsibilities
Design and maintain quality assurance protocols; perform quality inspections and evaluate production processes; process actions from quality system feedback (non-conforming materials, complaints, audits); assist with Design Control activities and sterilization/packaging validation; ensure compliance with governmental laws and regulations
Seniority
Entry-level, no previous professional experience