Quality Executive

Oji India Packaging

Chevuri

Vor Ort

INR 250.000 - 450.000

Vollzeit

Vor 13 Tagen

Eine vollständige Bewerbung in einer Minute

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Zusammenfassung

Oji India Packaging is seeking a QA/QC support profile to assist in QA/QC activities and documentation, aiming to reduce defects and improve inspections across packaging operations.

The role includes root cause analysis on customer complaints, CAPA implementation, and training the production and quality teams on quality standards and best practices. Familiarity with packaging testing standards is essential to drive continuous improvement.

Qualifikationen

  • Strong understanding of QA/QC principles and regulatory requirements.
  • Experience preparing QMS documents including CAPA and deviation notifications.
  • Familiarity with 7QC tools; knowledge of other QMS tools is a plus.

Aufgaben

  • Support in QA and QC activities.
  • Support in QA and QC documents.
  • Support in defects reductions and inspections.
  • Handle root cause analysis on customer complaints and implement CAPA.
  • Train production and quality team on quality standards and best practices.
  • Knowledge of packaging testing standards (BCT, ECT, Cobb, GSM, Bursting strength, etc).
  • Monitor quality KPI, prepare reports and drive continuous improvement activities.

Kenntnisse

QA principles
QC methods
Regulatory knowledge
Root cause analysis

Tools

QMS software
CAPA reports

Jobbeschreibung

Role & responsibilities


  • Support in QA and QC activities.

  • Support in QA and QC documents.

  • Support in defects reductions and Inspections.

  • Support in customer complaint handling perform root cause analysis and implement CAPA.

  • Train production and quality team on quality standards and best practices.

  • Knowledge of packaging testing standards (BCT, ECT, Cobb, GSM, Bursting strength etc.

  • Monitor quality KPI prepare reports and drive continuous improvement activities.


Desired Candidate Profile


  • Strong understanding of Quality Assurance principles, Quality Control methods, and regulatory requirements (e.g., FDA regulations).

  • Proficiency in preparing documents related to Quality Management Systems (QMS), including CAPA reports, deviation notifications, etc.

  • Familiarity with 7QC tools implementation is essential; knowledge of other QMS software applications an asset.

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