Product Quality Inspector

About the role

The Product Quality Inspector supports complex quality‑control activities within a medical‑device manufacturing environment. Working with limited supervision, the role ensures compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) while continuously improving product quality.

Key responsibilities

• Execute diverse quality‑control tasks, including in‑process and final inspections.
• Assist in diagnosing and resolving equipment malfunctions and process abnormalities.
• Document regulatory requirements and support validation protocols for new products and processes.
• Maintain equipment, follow safety protocols, and manage hazardous material handling.
• Escalate issues to superiors and contribute to planning and priority‑setting activities.
• Implement and monitor quality‑control procedures in line with GLP/GMP standards.

Required profile

• Minimum 4 years of manufacturing quality experience, preferably in the MedTech sector.
• Diploma in Electrical or Electronics engineering.
• Strong digital literacy and ability to work independently.

Required skills

• In‑Process and Outgoing Quality inspection.
• Final Quality assessment.
• DEFOA methodology.
• ISO 13485 knowledge.
• 21 CFR 820 familiarity.
• IPC A610 certification (preferred).
• Root Cause Analysis (RCA).
• Quality Management Systems (QMS) implementation.
• Technical documentation and regulatory requirements.