Overview

QMS Manager – Semiconductor Manufacturing Jobs in Ahmedabad, Gujarat, India at Best NanoTech

Title: QMS Manager – Semiconductor Manufacturing

Company: Best NanoTech

Location: Ahmedabad, Gujarat, India

QMS Manager Semiconductor Manufacturing

Location: Ahmedabad, Gujarat, India

Work Mode: Onsite

Employment Type: Full-Time

Experience: 10 -18 Years

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
  • Quality-system risk assessment
  • Continuous improvement

Audit Management

  • Internal quality audits
  • Customer audits
  • Certification audits
  • Supplier 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
  • Ishikawa diagrams
  • 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

  • Document lifecycle management
  • SOP and work-instruction control
  • Engineering change control
  • Manufacturing change control
  • Product and material change control
  • Electronic document-management systems
  • Training-record management
  • Record retention
  • Configuration and revision control
  • Product traceability

Leadership Responsibilities

  • Build and lead the site QMS and compliance organization.
  • Establish ownership for audit, CAPA, documentation and change-control activities.
  • Define quality-system responsibilities across manufacturing functions.
  • 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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