QC Team Leader

ResMed Inc; Kuala Lumpur; On-site; MYR 60,000 - 90,000; Full time

Job summary

ResMed Inc. in Johor Bahru (JB Tebrau) is seeking a Manufacturing Quality QC Team Leader to lead the QC Inspectors and ensure GMP-compliant quality control across goods inwards, in-process, and final production stages.

The role emphasizes strong leadership, process control, and continuous improvement in a high-volume manufacturing environment. The ideal candidate will have a tertiary degree in Engineering or Science, at least 2 years of industrial experience, and solid knowledge of FDA QSR, GMP,

Qualifications

• Tertiary qualification in Engineering or Science.
• Minimum 2 years of industrial experience, preferably in volume manufacturing.
• Solid knowledge of FDA QSR, GMP, and ISO standards.

Responsibilities

• Lead, motivate, and support QC Inspectors to meet daily goals.
• Oversee QC processes for incoming materials, in-process checks, and final production checks; drive issue resolution.
• Maintain GMP, 5S, and quality standards on the production floor and ensure proper housekeeping.
• Support calibration activities and drive continuous improvement; track KPI and SPC analyses.

Skills

GMP knowledge

Regulatory requirements

Leadership

Cross-functional collaboration

Analytical

Documentation

Education

Bachelor's degree in Engineering or Science

Tools

Microsoft Office

Oracle

Job description

## QC Team LeaderApply: MY JB Tebrau: Full time: Posted Today: JR\\_053497**Job Description** The primary role of Manufacturing Quality function is to design, implement and monitoring quality control programs. Key deliverables include, but not limited to, recommending changes to methods, procedures and standards to improve quality of output based on analysis of data and systems. Ensures products are built correctly to specification, quality standards and appropriate regulatory compliance. Reports defects and tracks until resolution. The **Quality Control Team Leader** is responsible for leading the QC team, ensuring compliance to quality systems, and supporting inspection activities across Goods Inwards, in‐process, and final production stages. The role emphasizes strong leadership, process control, continuous improvement, and adherence to GMP and safety standards.**Key Responsibilities** **Team Leadership*** Lead, motivate, and support QC Inspectors to meet daily operational goals.* Conduct training on procedures and product specifications; maintain LMS training records.* Mentor team members, identify development opportunities, and coordinate skills improvement.* Build strong working relationships with cross‐functional teams.* Ability to lead and support global projects or continuous improvement projects.* Support the calibration team in maintaining calibration systems and driving improvement. **QC Inspection & Reporting*** Oversee QC processes for incoming materials, in‐process checks, and outgoing checks.* Resolve daily QC issues using sound problem‐solving techniques.* Ensure records are properly maintained, filed, and archived without backlog.* Manage nonconforming materials and drive timely investigations and dispositions.* Improve QC processes and provide monthly KPI tracking, including SPC analysis. **Safety*** Support rehabilitation of injured employees and uphold Duty of Care obligations.* Promote safe work practices and prevent OH&S hazards, especially around manual handling. **GMP & Housekeeping*** Ensure GMP, 5S, and quality standards are consistently followed on the production floor.**Qualifications & Experience** **Core Competencies*** Strong understanding of GMP, quality systems, and regulatory requirements.* Ability to maintain process documentation and ensure product traceability.* Strong analytical capability for root cause and corrective action analysis.* Effective communication, leadership, and cross‐functional collaboration.* Able to manage multiple priorities with attention to detail.* Proficient in Microsoft, Oracle, and relevant software tools. **Required*** Tertiary qualification in Engineering or Science.* Minimum 2 years of industrial experience, preferably in volume manufacturing.* Solid knowledge of FDA QSR, GMP, and ISO standards. **Preferred*** Experience managing people or leadig teams.Joining us is more than saying “yes” to making the world a healthier place. It’s discovering a career that’s challenging, supportive and inspiring. Where a culture driven by excellence helps you not only meet your goals, but also create new ones. We focus on creating a diverse and inclusive culture, encouraging individual expression in the workplace and thrive on the innovative ideas this generates. If this sounds like the workplace for you, apply now!