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QMS Manager – Semiconductor Manufacturing

Best NanoTech

Ahmedabad, Gujarat, India · മുഴുവൻ സമയവും

അപേക്ഷിക്കുന്ന ആദ്യയാളാകൂ

അനുഭവം
10–18 yrs
ശമ്പളം
ഓപ്പണിംഗുകൾ
1
പോസ്റ്റ് ചെയ്തു
5 മണിക്കൂർ മുമ്പ്
പ്രവർത്തന രീതി
ഓഫീസിൽ
വിദ്യാഭ്യാസം
Bachelor's or Master's in Engineering/Quality Management/Manufacturing
പുനരാരംഭിക്കുക
അപേക്ഷിക്കാൻ നിർബന്ധം

നിങ്ങൾ എവിടെ ജോലി ചെയ്യും

ജോലി വിവരണം

Position Summary

Best NanoTech seeks an experienced QMS Manager to oversee the development, execution, and ongoing refinement of the Quality Management System (QMS) in a high-volume semiconductor assembly and test facility located in Ahmedabad, Gujarat, India. This full-time onsite role requires leadership in quality system governance, audit management, document and change control, CAPA processes, and adherence to semiconductor, automotive, and customer-specific quality standards.

Core Responsibilities

  • Create, deploy, and sustain the site’s Quality Management System ensuring compliance with standards like ISO 9001 and IATF 16949 as well as customer expectations.
  • Define and enforce quality policies, procedures, and work instructions alongside governance frameworks.
  • Lead and manage various audits including internal, external, customer, supplier, and certification audits with full cycle management from planning to closure.
  • Oversee CAPA, non-conformance handling, deviation management, and initiatives preventing recurrence.
  • Administer document control including approvals, revisions, distribution, retention, and electronic document management systems.
  • Drive manufacturing, product, material, and equipment change management processes effectively.
  • Conduct management reviews presenting QMS performance indicators, risks, and improvement strategies.
  • Define, monitor, and report quality KPIs, compliance dashboards, and early-warning indicators.
  • Champion risk management approaches including PFMEA, control plans, process audits, and 8D problem-solving methodologies.
  • Collaborate with cross-functional teams including manufacturing, process, equipment, product, quality, and reliability groups.
  • Support new product introductions and production ramp-ups from quality and compliance perspectives.
  • Manage customer-specific quality requirements and ensure traceability within site procedures.
  • Develop supplier quality governance, audit procedures, and corrective action processes.
  • Coordinate quality system training programs, competency development, and promote a quality-focused culture emphasizing disciplined execution and continuous improvement.
  • Prepare the site for regulatory, certification, and customer assessments ensuring QMS effectiveness in a 24/7 manufacturing environment.

Required Qualifications and Experience

  • Bachelor’s or Master’s degree in Engineering, Quality Management, Manufacturing, or related fields.
  • 10 to 18 years’ experience in quality systems, manufacturing quality, or compliance roles.
  • At least 4 to 6 years in a leadership role managing QMS teams or site-level quality initiatives.
  • Background in semiconductor, ATMP, OSAT, electronics, or similarly controlled high-volume manufacturing environments.
  • Strong familiarity with ISO 9001 standards and quality system auditing.
  • Preferred experience with IATF 16949, VDA 6.3, or automotive quality requirements.
  • Proven expertise in managing CAPA, change control, documentation, and management reviews.
  • Experience conducting certification, customer, and internal audits.
  • In-depth knowledge of risk-based quality management and statistical quality tools.
  • Ability to operate effectively across global and cross-functional teams.

Technical Expertise

  • QMS development and deployment
  • ISO 9001 and IATF 16949 compliance
  • Quality audits including internal, supplier, customer, process, product, and certification audits
  • Corrective and Preventive Actions (CAPA), 8D problem-solving, and root cause analysis techniques (5 Why, Ishikawa, Fault Tree)
  • Risk and process management tools such as PFMEA, control plans, SPC, process capability analyses, and quality gates
  • Document lifecycle and change control management including SOPs, training records, revision controls, and traceability systems

Leadership Responsibilities

  • Build and lead the site’s QMS and compliance team with clear ownership across audits, CAPA, documentation, and change management.
  • Define quality responsibilities across manufacturing functions and develop QMS personnel through structured training and mentoring programs.
  • Coordinate cross-departmental responses to audits and critical quality issues.
  • Establish governance forums for reviewing QMS performance and risk.
  • Drive a prevention-focused culture centered on quality and compliance principles.

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