Quality Control Executive

Biomed Global; Alor Gajah; On-site; MYR 30,000 - 50,000; Full time

Job summary

An established industry player is seeking a Quality Control Executive to enhance its QC team in Malacca. This vital role focuses on ensuring product quality and regulatory compliance, particularly in microbiological testing. The ideal candidate will conduct thorough QC testing, analyze data for trends, and maintain compliance with ISO 13485 standards. Fresh graduates with relevant academic backgrounds are encouraged to apply, making this an excellent opportunity for those looking to kickstart their careers in quality control within a supportive environment. Join a team dedicated to excellence and innovation in product quality!

Qualifications

• Degree in Microbiology or related field is required.
• Knowledge of ISO 13485 standards is advantageous.

Responsibilities

• Conduct QC testing of materials and culture media products.
• Analyze QC data and report deviations from specifications.
• Train production personnel on QC procedures.

Skills

Microbiological Testing

Analytical Skills

Attention to Detail

Quality Standards Compliance

Education

Diploma in Microbiology

Bachelor's Degree in Biomedical Science

Medical Laboratory Science

Tools

QC Equipment

Job description

Position Title: Quality Control Executive

Location: Malacca, Malaysia

Position Type: Contract

Position Overview:

We are currently seeking a dedicated and detail-oriented Quality Control Executive to join our QC team in Malacca. This role plays a key part in ensuring product quality and regulatory compliance, with a strong focus on microbiological testing—particularly for culture media and sterility.

Key Responsibilities:

• Conduct and document QC testing of raw materials, in-process materials, and finished culture media products in compliance with established protocols and regulatory standards.
• Analyze QC data, identify trends, and report deviations from specifications.
• Investigate non-conformances and implement corrective and preventive actions (CAPA).
• Maintain accurate and timely QC records, ensuring documentation meets regulatory and ISO 13485 requirements.
• Assist in developing and maintaining SOPs, quality procedures, and internal documentation.
• Conduct internal audits to monitor compliance with internal standards and external regulations.
• Ensure timely calibration and maintenance of QC equipment; report any equipment-related issues.
• Identify process improvement opportunities to enhance QC efficiency and reduce error.
• Train production personnel on QC procedures.
• Investigate and respond to customer complaints regarding product quality, ensuring preventive measures are implemented.
• Monitor quality of materials from external vendors and collaborate to resolve issues.
• Carry out additional duties as assigned by management.

Requirements:

• Diploma or Bachelor's degree in Microbiology, Biomedical Science, Medical Laboratory Science, or a related field.
• Knowledge of microbiological testing, especially in prepared culture media and sterility testing, is an advantage.
• Strong analytical skills, attention to detail, and commitment to quality standards.
• Ability to work both independently and as part of a team in a regulated environment.
• Familiarity with ISO 13485 standards is added advantage.

*Fresh graduates with relevant academic or lab experience are encouraged to apply.