Supervisor QA Product Release

Dexcom; Seberang Perai; On-site; MYR 70,000 - 100,000; Full time

Job summary

A leading medical technology company in Penang is seeking a Supervisor QA Product Release to manage quality assurance processes and supervise inspection personnel. The ideal candidate will have a Bachelor's degree and 5-8 years of experience in the Medical Device or Manufacturing industry. Key responsibilities include coordinating inspections, ensuring compliance with quality standards, and leading cross-functional teams to support quality and business objectives. Strong leadership, communication, and problem-solving skills are essential for success in this fast-paced environment.

Qualifications

• 5-8 years of experience in the Medical Device or Manufacturing industry.
• Strong understanding of applicable regulations and industry standards.
• Previous experience in a regulated industry is preferred.

Responsibilities

• Manage quality assurance processes and inspection personnel.
• Coordinate tasks and work plans in the Product Release area.
• Ensure compliance with quality standards and conduct audits.

Skills

Leadership

Quality management systems

Communication

Team collaboration

Problem-solving

Education

Bachelor's degree

Tools

Microsoft Office

Job description

Supervisor QA Product Release manages in maintaining high-quality standards by supporting quality assurance processes, coordinating inspections, and managing DHR/LHR documentation, contributing to the overall quality and compliance of products or services within an organization.

Where you come in:

As a member of the QA Product Release team, you play a vital role in ensuring the quality and compliance of DHR/LHR review. Your work supports operational efficiency, sustainability, and adherence to regulatory and internal standards.

What makes you successful:

You will perform supervisory and administrative duties associated with inspection personnel management.

You will provide direct supervision to support individual contributors/matrix reports.

You will coordinate the tasks and work plans of the Product Release area.

You will verify the accuracy and adequacy of inspection activities and DHR/LHR records, while maintaining accurate and detailed documentation of all in-process and outgoing quality control activities.

You will generate and maintain quality metrics and reports, as required, and implement appropriate preventive/corrective actions (as needed) to improve quality. Maintains component and supplier performance data and assists with supplier quality management.

You will identify problems and propose solutions that are timely, cost-effective, and meet quality requirements.

You will work with QA, Manufacturing, Engineering, Supply chain, as necessary, to support quality and business objectives.

You will support routine audit readiness activities including conducting regular Gemba walks, inspections and audits to ensure compliance with quality standards.

You will plan, manage and prioritize tasks/projects, tracks progress toward overall goals, and provide periodic updates to management.

Experience and Education Requirements:

Typically requires a Bachelor’s degree with 5-8 years of Medical Device or Manufacturing industry. Informal management/ team lead experience.

Strong understanding of quality management systems, applicable regulations, and industry standards (e.g., ISO 13485).

Excellent leadership and communication skills, with the ability to work collaboratively across cross-functional teams and remain hands-on in a fast-paced environment.

Proficiency with Microsoft Office Products.

Previous direct involvement in the medical device industry or a regulated industry.

Ability to run self-directed projects, maintain timelines, transfer technology, and execute projects in an R&D and GMP manufacturing environment.

Ability to deal with ambiguity/uncertainty and a willingness to try new/challenging things.

Strong interpersonal and teamwork skills.

Demonstrated written and verbal communication skills.