QMS Manager – Semiconductor Manufacturing

Best NanoTech

Ahmedabad District

On-site

INR 1,500,000 - 2,800,000

Full time

4 days ago
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Job summary

Best NanoTech in India is seeking a QMS Manager to establish, implement and continually improve the Quality Management System for a high-volume semiconductor assembly and test facility.

The role covers governance, audit readiness, document control, CAPA and compliance with semiconductor, automotive and customer requirements, requiring strong experience in controlled manufacturing environments.

Qualifications

  • Bachelor's or Master's degree in Engineering, Quality Management, Manufacturing or related discipline.
  • 10-18 years of experience in quality systems, manufacturing quality or compliance.
  • Minimum 4-6 years of experience managing QMS teams or site-level quality programs.
  • Experience in semiconductor, ATMP, OSAT or other high-volume controlled manufacturing environment.
  • Strong knowledge of ISO 9001 and quality-system auditing.
  • Experience with IATF 16949, VDA 6.3 or automotive-quality requirements is preferred.
  • Demonstrated experience managing CAPA, change control, document control and management reviews.
  • Experience leading certification, customer and internal audits.
  • Strong knowledge of risk-based quality management and statistical quality tools.

Responsibilities

  • Develop, implement and maintain the site Quality Management System.
  • Ensure compliance with ISO 9001, IATF 16949 and applicable customer requirements.
  • Establish quality policies, procedures, work instructions and governance mechanisms.
  • Lead internal, external, customer, supplier and certification audits.
  • Manage audit planning, execution, findings, corrective actions and closure.
  • Own CAPA, non-conformance, deviation and recurrence-prevention processes.
  • Establish and control document approval, revision, distribution and retention systems.
  • Lead manufacturing, product, material and equipment change-control processes.
  • Facilitate management reviews and present QMS performance, risks and improvement plans.
  • Define and monitor quality KPIs, compliance dashboards and early-warning indicators.
  • Drive PFMEA, control-plan, process-audit and risk-management deployment.
  • Ensure effective implementation of 8D and root-cause-analysis methodologies.
  • Partner with manufacturing, process, equipment, product, quality and reliability teams.
  • Support new-product introduction and production ramp from a QMS and compliance perspective.
  • Manage customer-specific requirements and maintain traceability to site procedures.
  • Develop supplier-quality governance, audit and corrective-action processes.
  • Coordinate quality-system training, awareness and competency development.
  • Promote quality culture, disciplined execution and continuous improvement.
  • Lead preparation for regulatory, certification and customer assessments.
  • Ensure QMS effectiveness across 24 7 manufacturing operations.

Skills

QMS development
ISO 9001
IATF 16949
Audit management
CAPA & 8D
Risk-based thinking
Process improvement

Education

Bachelor's or Master's degree in Engineering/Quality Management

Tools

Electronic document-management systems
Configuration and revision control

Job description

Industry: Semiconductor / ATMP / OSAT / Electronics Manufacturing

Role Overview

We are looking for a QMS Manager to establish, implement and continuously improve the Quality Management System for a high-volume semiconductor assembly and test manufacturing facility.

The role will own quality-system governance, audit readiness, document control, change management, CAPA and compliance with applicable semiconductor, automotive and customer-quality requirements. The position requires strong experience in semiconductor, electronics or other highly controlled manufacturing environments.

Key Responsibilities
  • Develop, implement and maintain the site Quality Management System.
  • Ensure compliance with ISO 9001, IATF 16949 and applicable customer requirements.
  • Establish quality policies, procedures, work instructions and governance mechanisms.
  • Lead internal, external, customer, supplier and certification audits.
  • Manage audit planning, execution, findings, corrective actions and closure.
  • Own CAPA, non-conformance, deviation and recurrence-prevention processes.
  • Establish and control document approval, revision, distribution and retention systems.
  • Lead manufacturing, product, material and equipment change-control processes.
  • Facilitate management reviews and present QMS performance, risks and improvement plans.
  • Define and monitor quality KPIs, compliance dashboards and early-warning indicators.
  • Drive PFMEA, control-plan, process-audit and risk-management deployment.
  • Ensure effective implementation of 8D and root-cause-analysis methodologies.
  • Partner with manufacturing, process, equipment, product, quality and reliability teams.
  • Support new-product introduction and production ramp from a QMS and compliance perspective.
  • Manage customer-specific requirements and maintain traceability to site procedures.
  • Develop supplier-quality governance, audit and corrective-action processes.
  • Coordinate quality-system training, awareness and competency development.
  • Promote quality culture, disciplined execution and continuous improvement.
  • Lead preparation for regulatory, certification and customer assessments.
  • Ensure QMS effectiveness across 24 7 manufacturing operations.
Required Qualifications
  • Bachelor s or Master s degree in Engineering, Quality Management, Manufacturing or a related discipline.
  • 10 18 years of experience in quality systems, manufacturing quality or compliance.
  • Minimum 4 6 years of experience managing QMS teams or site-level quality programs.
  • Experience in semiconductor, ATMP, OSAT, electronics or another high-volume controlled manufacturing environment.
  • Strong working knowledge of ISO 9001 and quality-system auditing.
  • Experience with IATF 16949, VDA 6.3 or automotive-quality requirements is preferred.
  • Demonstrated experience managing CAPA, change control, document control and management reviews.
  • Experience leading certification, customer and internal audits.
  • Strong knowledge of risk-based quality management and statistical quality tools.
  • Ability to work across global and cross-functional organizations.
Technical Skills Quality Management Systems
  • QMS development and implementation
  • ISO 9001
  • IATF 16949
  • Quality policy and objectives
  • Management review
  • Process-based auditing
  • Quality KPI management
  • Customer-specific requirements
Audit Management
  • Internal quality audits
  • Process and product audits
  • VDA 6.3
  • Audit schedules and checklists
  • Non-conformity management
  • Corrective-action verification
  • Audit-readiness programs
CAPA and Problem-Solving
  • Corrective and Preventive Action
  • 8D problem-solving
  • Root-cause analysis
  • 5 Why analysis
  • Fault Tree Analysis
  • Containment and recurrence prevention
  • Effectiveness verification
  • Non-conformance management
  • Deviation and concession control
Process and Risk Management
  • PFMEA
  • Control plans
  • Statistical Process Control
  • Process Capability Analysis
  • Measurement System Analysis
  • Change-point management
  • Risk-based thinking
  • Quality gates
  • Process validation
  • Product and process release
Document and Change Control
  • SOP and work-instruction control
  • Manufacturing change control
  • Product and material change control
  • Electronic document-management systems
  • Training-record management
  • Configuration and revision control
Leadership Responsibilities
  • Build and lead the site QMS and compliance organization.
  • Establish ownership for audit, CAPA, documentation and change-control activities.
  • Develop QMS engineers and auditors through structured training and mentoring.
  • Coordinate cross-functional responses to audits and significant quality issues.
  • Establish governance forums for QMS performance and risk review.
  • Promote a prevention-based culture focused on quality and compliance.
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