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