QC Supervisor (Medical Devices) -LY12

THE SUPREME HR ADVISORY PTE. LTD.; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A leading advisory firm in Singapore seeks a QC Supervisor to oversee daily quality control operations. The role involves leading a diverse team, ensuring compliance with ISO standards, and implementing quality improvements. Candidates should demonstrate strong leadership and knowledge of quality control practices.

Qualifications

• Able to lead a diverse team.
• Working knowledge of ISO 13483:2016 preferred.
• Familiarity with quality control tools and test equipment required.

Responsibilities

• Lead supervise a team of QC inspectors for daily activities.
• Implement and document quality procedures and workflows.
• Monitor quality control trends and team performance.

Skills

Leadership

Quality Control

Continuous Improvement

Coaching

Tools

Quality Control Tools

Test Equipment

Job description

• QC Supervisor
• Working Location: Buroh Street (Boon Lay)
• Working Days: 5 Days Work, Monday - Friday
• Working Hours: 8:30 am - 6:30pm
• Salary Range: Up to $3500 Depends on Experience

Interested applicants can also send your resume to WA: [phone] (Ms Lynne) and allow our Consultant to match you with our Clients. No Charges will be incurred by Candidates for any service rendered.

TAN LEE XIAN Reg No: R24123487

The Supreme HR Advisory Pte Ltd EA No: 14C7279

Key Roles & Responsibilities

• Lead and Supervise a team of QC inspector overseeing daily QC inspection activities in compliance with established standards.
• Provide training, coaching and mentoring to enhance the skills and performance of team members.
• Prepare and maintain work schedule for the department to ensure optimize resource for overall efficiency.
• Work with cross-functional teams to implement continous improvement, track status of non-conformities and CAPA effectiveness.
• Responsible for review and approval of DHR. Ensure quality records and samples are retained complying with good writing practices GDP requirements.
• Implement quality documentation changes, such as QC procedures, process workflows, work instruction, etc. guide the team to follow through the changes.
• Review and submit validation of verification measurement reports.
• Perform daily process audit to meet quality operational requirements.
• Ensure product identification and traceability of product are in place.
• As Calibration administrator, ensure equipment are calibrated correctly, provided accurate measurements and having proper identification.
• Assists in customer complaint analysis, investigation of quality issues and corresponding improvement measures.
• Authorize the release (COC) of products, COA review and approval.
• Adhere to safety protocols and implement preventive measure to maintain a safe working environment.
• Monitor and report KPI of QC team job performance, production quality trends, quality control charts, etc.
• Any other task as assigned by the superior.

Requirements

• Able to lead a diverse team
• Working knowledge on ISO 13483: 2016 and quality assurance / quality control of medical devices is an added advantages
• Familiar with use of various quality control tools and test equipment