QC Supervisor [ISO 13483: 2016 | Medical Device]

The Supreme HR Advisory Pte Ltd; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

An established industry player is seeking a QC Supervisor to lead a dynamic team in ensuring quality standards for medical devices. This role involves supervising daily inspection activities, providing training, and collaborating with cross-functional teams to drive continuous improvement. You will oversee quality documentation changes and conduct audits to maintain compliance, while also analyzing customer complaints to implement effective solutions. If you are passionate about quality assurance and possess strong leadership skills, this opportunity is perfect for you.

Benefits

Company Benefits

Incentives

Qualifications

• Strong leadership skills to manage a diverse QC team.
• Knowledge of ISO standards is an advantage.

Responsibilities

• Lead and supervise QC inspectors to ensure compliance with standards.
• Provide training and coaching to enhance team performance.
• Conduct audits and ensure quality standards are met.

Skills

Team Leadership

Quality Control

ISO 13485:2016 Knowledge

Problem Solving

Tools

Quality Control Tools

Test Equipment

Job description

QC Supervisor Position at Boon Lay

Location: Boon Lay

Salary Package: Attractive salary, up to $3500 depending on experience

Benefits & Incentives: Company benefits and incentives provided

Application: Interested applicants can send your resume to [phone] (Han) or [e-mail]. Our consultant will match you with suitable clients. No charges apply to candidates for any services.

Job Details

• Working Days: Monday to Friday, 5 days a week
• Working Hours: 8:30 am - 6:30 pm

Key Roles & Responsibilities

• Lead and supervise a team of QC inspectors, overseeing daily inspection activities in compliance with standards.
• Provide training, coaching, and mentoring to improve team performance.
• Prepare and maintain work schedules to optimize resources and efficiency.
• Collaborate with cross-functional teams to implement continuous improvement, track non-conformities, and evaluate CAPA effectiveness.
• Review and approve DHRs, ensuring quality records and samples are retained according to GDP requirements.
• Implement changes in quality documentation, such as procedures and work instructions, guiding the team through these updates.
• Review and validate verification measurement reports.
• Conduct daily process audits to ensure quality standards are met.
• Ensure proper product identification and traceability.
• As Calibration Administrator, oversee equipment calibration to ensure accuracy and proper identification.
• Assist in analyzing customer complaints, investigating quality issues, and implementing improvements.
• Authorize product release (Certificate of Conformance), review, and approve Certificates of Analysis.
• Adhere to safety protocols and promote a safe working environment.
• Monitor and report on KPI, quality trends, and control charts.
• Perform any other tasks assigned by superiors.

Requirements

• Ability to lead a diverse team.
• Knowledge of ISO 13485:2016 and quality assurance/control of medical devices is an advantage.
• Familiarity with quality control tools and test equipment.

Contact us via WhatsApp: https://wa.me/6596420989 or call [phone] (Han). Email: [e-mail].

Chaw Chiaw Han, Reg No: R22106723

The Supreme HR Advisory Pte Ltd, EA No: 14C7279