Quality Control Inspector Jobs in Coimbatore Medical Device Company

📋 Job Description

Jobzi is sourcing qualified candidates for Quality Control Inspector positions in Coimbatore's private Medical Device Company sector. This is a full-time opportunity with a reputed Medical Device and Equipment employer in Coimbatore offering competitive salary, structured growth, and a professional work environment. Tamil communication skills are preferred alongside English for professional and business interaction in Coimbatore.

📌 Key Responsibilities

• Perform incoming quality inspection of raw materials, components, and packaging using AQL sampling plans
• Conduct in-process inspection at defined control points during device assembly
• Inspect finished devices against approved specifications and acceptance criteria
• Maintain inspection records, NCR logs, and device history records
• Calibrate and verify measuring instruments such as vernier callipers, micrometers, and gauges
• Coordinate with production supervisors on non-conformance disposition and CAPA actions
• Prepare daily quality reports and escalate critical defects to QA management

🎓 Qualifications and Requirements

• Which inspection instruments have you used - vernier, micrometer, or vision systems?
• Have you worked with AQL sampling plans and how do you apply them?
• What types of medical devices or components have you inspected?
• Are you familiar with device history records and non-conformance reporting?
• Have you participated in an ISO 13485 internal audit?
• Can you read engineering drawings and inspection checklists?
• Have you handled customer or regulatory inspection visits?
• Good Tamil and English communication skills for team coordination and client interaction in Coimbatore.

✅ Required Skills

🏆 Certifications and Qualifications

B.E./B.Tech. (Biomedical, Mechanical, or Electronics) for engineering and field service roles; M.Sc. or B.Sc. in Life Sciences for IVD application and quality roles; ISO 13485 quality management system training; CDSCO MDR 2017 regulatory compliance knowledge for regulatory affairs roles; IEC 60601 and CE marking awareness for quality roles; Lean Manufacturing and GMP training for production roles; BLS and medical device demonstration certification for clinical sales specialists