Job Description

Key Responsibilities:

Conduct in-process and final inspection of products as per standard operating procedures (SOPs) and quality specifications. Inspect raw materials, components, and packaging materials before use. Record and document inspection results accurately and maintain inspection reports. Identify non-conformities and coordinate with production and QA teams for corrective actions. Ensure all measuring and testing instruments are calibrated and functioning properly. Assist in implementation of Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP). Participate in root cause analysis and quality improvement initiatives. Support internal and external audits as required. Follow all safety, hygiene, and compliance standards as per ISO and regulatory guidelines.

Qualifications & Skills:

Education:

Diploma or B.Sc./B.Tech in Mechanical, Industrial, or Biomedical Engineering, or related field.

Experience:

1-3 years of experience in quality inspection, preferably in the medical devices manufacturing industry.

Knowledge:

Understanding of ISO 13485, GMP, and quality control principles. Familiarity with inspection tools and measuring instruments (vernier calipers, micrometers, etc.). Basic understanding of regulatory standards (e.g., CE, FDA, MDR).

Skills:

Strong attention to detail and analytical ability. Good communication and reporting skills. Ability to work independently and in a team

Interested candidates may apply by sharing their updated CV at hrd@larsmedicare.com or WhatsApp it to +91 8930111001.

Job Type: Full-time

Pay: ?12,000.00 - ?25,000.00 per month

Work Location: In person