Quality Engineer

Company Description

Vispala Technologies is a leading Indian provider of assistive technology products and services.

Location: Kolkata (Main Office)

Industry: Medical Devices/Prosthetics

For detail please visit www.vispala.com

Role Summary

We are looking for a full-time, on-site, Quality Engineer to join our manufacturing team. The role involves close coordination with R&D, Production, and After-Sales teams to ensure product quality, compliance, and continuous improvement.

The Quality Engineer will be responsible for supporting the development and implementation of quality control and assurance processes. Daily tasks include evaluating product quality, developing quality metrics, collaborating with cross-functional teams to address quality issues, and ensuring compliance with quality management standards. The role requires a proactive approach to identifying potential areas for process improvement and executing measures to ensure high-quality outcomes.

Key Responsibilities

• Work closely with the R&D and Production teams to ensure quality standards are met at every stage
• Inspect and measure all mechanical parts using appropriate measuring tools and maintain inspection records
• Perform final product inspection, including dimensional checks, functional testing, and performance testing
• Prepare and maintain quality inspection sheets, measurement reports, and test records
• Handle ISO 13485 documentation, including

Daily quality records

New Development Forms

Change Request Forms

• Maintain and calibrate mechanical and electronic tools used in QC and production
• Monitor manufacturing processes and identify quality issues or deviations
• Support mass production and export quality requirements
• Coordinate with the after-sales team and clients to address quality complaints
• Generate trouble tickets and coordinate with relevant teams for root cause analysis and corrective action
• Ensure compliance with internal SOPs, quality standards, and regulatory requirements

Qualifications

• Bachelor's degree in Engineering, Quality Management, or a related field
• 3+ years experience in quality control (medical device manufacturing preferred)
• Knowledge of ISO 13485 process (mandatory)
• Basic understanding of mechanical components and measurements
• Hands-on experience with mechanical measuring instruments
• Familiarity with documentation and quality records management
• Ability to work cross-functionally with R&D, Production, and Service teams
• Good communication and coordination skills
• Strong attention to detail and problem-solving mindset