Senior Quality Control Supervisor

About the role

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.

Continuous Improvement:

• 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.