QA/QC Analyst — Manufacturing & GMP Excellence

BEAUTY ELEMENTS VENTURES MANUFACTURING INC.; Mimaropa; On-site; PHP 250,000 - 420,000; Full time

Job summary

Beauty Elements Ventures Manufacturing Inc. is seeking a QA/QC Analyst with a BS Biology or related science background to ensure quality during production. The role requires hands-on raw materials inspection, data trend analysis, and strong attention to detail under production pressure.

Experience in manufacturing settings and 1+ year in QA/QC is preferred. You will monitor GMP compliance, verify process lines, manage sampling and tray setup, and prepare daily QA inspection and CAPA reports

Qualifications

• Requires BS Biology or related science/health background.
• 1+ years of QA/QC Analyst experience in manufacturing.
• Hands-on experience in raw materials inspection and verification.
• Proficient in data trend analysis and critical problem-solving.
• Exceptional attention to detail and sound decision-making under production pressure.

Responsibilities

• Inventory & Setup Verification: Validates daily mixing schedules and checks accuracy of dispensed materials per tank.
• Process & GMP Monitoring: Oversees machines, personnel, and strict GMP compliance in manufacturing and compounding.
• Quality & Sampling Controls: Evaluates bulk attributes, manages tray setup, and submits lab samples.
• Data Tracking & Reporting: Analyzes soap rejection trends, reviews MR entries, and provides QA reports and CAPA.
• Team & Superior Support: Assists the mixing team leader and supports supervisors.

Skills

Data trend analysis

Critical problem-solving

Attention to detail

Decision-making under pressure

Education

BS Biology or related science/health

Job description

Beauty Elements Ventures Manufacturing Inc. is seeking a QA/QC Analyst with a BS Biology or related science background to ensure quality during production. The role requires hands-on raw materials inspection, data trend analysis, and strong attention to detail under production pressure.

Experience in manufacturing settings and 1+ year in QA/QC is preferred. You will monitor GMP compliance, verify process lines, manage sampling and tray setup, and prepare daily QA inspection and CAPA reports