Quality Control Analyst

Cosmetique Asia Corporation; Bulacan; On-site; PHP 279,000 - 391,000; Full time

Job summary

Cosmetique Asia Corporation seeks a meticulous QC Analyst in Bulacan to ensure products meet regulatory, safety, and internal standards. You will monitor, test, and verify quality throughout production, applying GLP/GMP practices and robust documentation control.

Requirements include a chemistry-related degree and at least 6 months in manufacturing. You will work in Plaridel, Bulacan, with opportunities to develop analytical skills and contribute to continuous improvement in quality systems.

Qualifications

• Bachelor’s degree in Chemistry, Chemical Technology, or related field.
• At least 6 months of work experience in a manufacturing setting.
• Strong communication, analytical and decision-making abilities.
• Familiarity with GLP, GMP, QC tools, calibration, and test methods.
• Willing to be assigned to Plaridel, Bulacan.

Responsibilities

• Monitor, test, and verify that products meet regulatory, safety, and company standards.
• Maintain documentation and support corrective and preventive actions.

Skills

Strong communication

Analytical thinking

Decision-making abilities

Statistical analysis

Root cause analysis

Document control

Acceptance sampling

Test methods

GLP

QC tools

Calibration

GMP

Chemical handling

Corrective/preventive actions

Education

Bachelor’s degree in Chemistry, Chemical Technology, or related field

Job description

Job Description

- The QC Analyst will play a crucial role in ensuring the highest standards of quality. He/She will be responsible for monitoring, testing, and verifying that products meet regulatory, safety, and company standards.

Qualifications

• Bachelor’s degree in Chemistry, Chemical Technology, or a related field.
• At least six (6) months of work experience in a manufacturing company (preferably in a related industry).
• Strong communication, analytical, and decision-making abilities.
• Proficiency in statistical analysis, root cause analysis, and document control.
• Familiarity with acceptance sampling, test methods, GLP (Good Laboratory Practices), QC tools, calibration, Halal standards, GMP (Good Manufacturing Practices), chemical handling, root cause analysis, and corrective/preventive actions.
• Willing to be assigned to Plaridel, Bulacan.