Quality Assurance Specialist (Freelance)

Location: Grenoble, France (Hybrid)

Start Date: June 2026

Contract Length: 12 months (freelance)

Key Responsibilities:

• Support the effective operation of the Quality Management System through document control, record maintenance, and procedural updates
• Coordinate training activities, maintain training records, and support supplier documentation and quality agreement updates
• Monitor quality system performance by collecting, analysing, and reporting KPI data and trends for management review
• Identify quality system gaps or non‑conformances and contribute to investigations and escalation where appropriate
• Assist with internal audits, corrective and preventive actions (CAPA), and verification of follow‑up activities
• Support preparation for, and participation in, external audits and regulatory assessments
• Collaborate closely with cross‑functional teams to resolve quality issues efficiently and support continuous improvement
• Contribute as an active member of the Quality team, ensuring clear communication and alignment across departments

Requirements:

• Degree or equivalent qualification in a scientific, engineering, or life science‑related discipline
• Minimum of 5 years' experience working in a regulated quality environment in medical devices.
• Practical experience supporting Quality Management Systems, including documentation control, audits, and CAPA activities
• Good working knowledge of regulatory and quality standards (ISO 13485, FDA 21 CFR Part 820, MDSAP or similar)
• Strong organisational, communication, and data‑handling skills, with confidence using MS Office and document management tools