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Quality Incharge

Manufacturing | Quality assurance Manager

25,000 - 50,000 p.m | Under Graduate - Bachelor of Management , Bachelor of Engineering / Technology - MECHANICAL ENGINGEERING | Chennai

kundrathur

Gender : All | Age Limit - 18-35 | Openings - 5 | Experience - 4-5 Years | Job Type - Regular

Posted Jobs Count : 3

Open Until : 30-06-2026

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Key Responsibilities

1. Quality Planning (From Job Card Stage)

Review job cards, engineering drawings, and technical specifications.
Prepare Quality Plans, Inspection Test Plans (ITP), and checklists for each job.
Define critical quality checkpoints across all stages of production.
Ensure all quality requirements are clearly communicated before production starts.

2. End-to-End Quality Control (Job Card to Assembly)

Monitor and control quality at all stages:
- Incoming raw materials
- Fabrication and machining
- Sub-assemblies
- Final assembly and finishing
Approve stage-wise completion before moving to the next process.
Ensure traceability of materials and components as per job card.
Verify that final assembly meets functional and safety requirements.

3. Inspection & Testing Management

Oversee incoming, in-process, and final inspections.
Ensure proper use and calibration of measuring and testing instruments.
Validate test results and approve final product release.
Maintain records such as inspection reports, test certificates, and quality logs.

4. Coordination & Cross-Functional Integration

Coordinate with:
- Production – to ensure adherence to quality standards
- Design/Engineering – for clarifications and changes
- Procurement – for supplier quality issues
- Stores – for material quality and traceability
Ensure smooth communication of quality requirements across departments.

5. Non-Conformance & CAPA Management

6. Budgeting & Cost of Quality

Prepare and manage quality-related budgets (inspection tools, testing equipment, training).
Monitor cost of poor quality (COPQ): scrap, rework, rejection, warranty claims.
Implement measures to reduce defects and improve first-time-right production.
Optimize inspection processes to balance cost and compliance.

7. Regulatory Compliance & Audits

Ensure compliance with medical device standards such as ISO 13485, GMP, and applicable regulatory requirements.
Maintain proper documentation for audits and certifications.
Lead internal audits and support external/customer audits.
Ensure document control and record retention as per standards.

8. Team Leadership