Senior Quality Control Supervisor

KLS Martin Malaysia Sdn Bhd

Simpang Ampat

In loco

MYR 60.000 - 90.000

Tempo pieno

2 giorni fa
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Descrizione del lavoro

KLS Martin Malaysia Sdn Bhd is seeking a QC Supervisor to oversee quality control processes in our medical device manufacturing facility in Penang. You will lead a QC team, ensure adherence to procedures, and drive continuous improvement.

The role requires a Diploma or Certificate with at least 2 years in medical device manufacturing, strong teamwork, and the ability to read technical English. You will monitor quality data, conduct audits, implement corrective actions, and maintain documentation

Competenze

  • Diploma or Certificate in a related field.
  • Minimum 2 years of experience in medical device manufacturing.
  • Ability to read and write English and interpret technical documents.

Mansioni

  • Lead and manage the QC team, including junior and senior personnel.
  • Develop, implement, and maintain quality control procedures and standards.
  • Conduct regular inspections and audits to ensure compliance.
  • Monitor and analyze quality data to identify trends and areas for improvement.
  • Recommend and implement corrective and preventive actions.
  • Oversee product testing and inspection activities to verify specifications.
  • Maintain accurate records of QC activities and prepare reports.
  • Communicate quality issues to stakeholders in a timely manner.
  • Lead or participate in quality improvement projects.

Formazione

Diploma or Certificate in related field
2+ years in medical device manufacturing

Descrizione del lavoro

The Quality Control (QC) Supervisor oversees the quality control processes within the organization to ensure that products meet established quality standards. They are responsible for managing both junior and senior QC functions, ensuring adherence to procedures, and driving continuous improvement initiatives.

Key responsibilities

Supervision and Leadership:

Lead and manage the QC team, including both junior and senior QC personnel.

Provide guidance, training, and support to junior QC staff.

Delegate tasks effectively and ensure that responsibilities are clearly defined within the team.

Quality Control Processes:

Develop, implement, and maintain quality control procedures and standards.

Conduct regular inspections and audits to ensure compliance with quality requirements.

Monitor and analyze quality data to identify trends, issues, and areas for improvement.

Recommend and implement corrective and preventive actions to address quality issues.

Product Testing and Inspection:

Oversee product testing and inspection activities to verify compliance with specifications and standards.

Review test results and inspection reports to ensure accuracy and completeness.

Investigate and resolve any discrepancies or deviations from quality standards.

Documentation and Reporting:

Maintain accurate and up-to-date records of quality control activities, including test results, inspection reports, and corrective actions.

Prepare regular reports on quality performance metrics and trends for management review.

Communicate quality issues and findings to relevant stakeholders in a timely manner.

Identify opportunities for process improvement and efficiency gains within the QC function.

Lead or participate in quality improvement projects and initiatives.

Implement best practices and lessons learned to enhance quality control processes.

Other responsibilities may be assigned from time to time as needed.

Qualification / Education Background

Minimum qualification is Diploma or Certificate with 2 years and above working experience in Medical Device Manufacturing

Experience

Possess with at least 2 years of working experience in Medical Device Manufacturing.

Direct and indirect supervisory experience with ability to work in a team environment.

Demonstrates leadership.

Ability to read and write English and interpret documents such as technical manuals etc.

Preferred Knowledge

Knowledge of quality systems and standards such as GMP, ISO 13485 Standard etc.

Good organizational skills and attains ability to communicate effectively with others.

Manufacturing background with highly automated equipment.

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