CHARGE.E QUALITE SYSTEMES
Core
Maintaining and improving industrial site quality systems in compliance with regulatory requirements and applicable standards.
Role type
Quality Assurance Systems Specialist
Builds
Quality management systems, documentation, audit processes, and CAPA workflows
Domain
Pharmaceutical/Cosmetic/Chemical/Medical Devices Industry + Quality Assurance
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Quality Assurance principles, document management systems, audit processes, CAPA methodology, regulatory standard knowledge, performance indicator tracking, supplier quality evaluation, corrective and preventive action (CAPA) management, internal audit coordination, client audit preparation, quality investigation analysis
Preferred skills
Experience in regulated environments, stakeholder management, cross-functional project collaboration
Responsibilities
Pilot and animate quality processes including documentation, internal audits, anomalies, CAPA, and Change Control; Maintain and improve the quality documentation system; Coordinate the Site Quality Committee; Deploy and track quality system performance indicators; Conduct training sessions; Evaluate and follow up on industrial service providers including audits and corrective actions; Participate in internal, client, and regulatory inspections; Contribute to quality anomaly investigations and continuous improvement projects
