Quality Assurance (QA) Inspector

LORENZO C. REYES LABORATORY, INC.; Malolos; On-site; PHP 290,000 - 513,000; Full time

Job summary

LORENZO C. REYES LABORATORY, INC. is seeking a detail-oriented Quality Control Analyst to join our pharmaceutical manufacturing team in Bulacan.

You will perform production line clearance, in-process inspections, and material inspections while ensuring strict adherence to cGMP, GDP, and FDA standards. Fresh graduates are encouraged to apply. The role emphasizes documentation review, CAPA support, and product release activities, with a focus on accuracy, compliance, and timely reporting in a

Qualifications

• Bachelor’s degree in Pharmacy or related scientific field.
• Fresh graduates are encouraged to apply.
• Knowledge of cGMP, GDP, and FDA regulations is an advantage.
• Experience in pharmaceutical, cosmetics, food, or FDA-regulated manufacturing industries preferred.
• Strong attention to detail and observation skills.
• Proficient in documentation and basic computer applications.

Responsibilities

• Production line clearance and monitoring
• In-process inspection and quality monitoring
• Raw materials, packaging materials and finished product inspection
• Warehouse and good storage practice monitoring
• Documentation review and compliance verification
• FDA, cGMP and GLP compliance
• Deviation, non-conformance and CAPA support
• Product release support

Skills

Attention to Detail

Communication Skills

Analytical Thinking

Organizational Skills

Documentation Proficiency

Basic Computer Skills

Education

Bachelor's Degree in Pharmacy or related scientific field

Job description

I. Qualifications

• Bachelor's Degree in Pharmacy, Chemistry, Biology, Microbiology, Chemical Engineering, or related scientific field.
• Preferably with experience in pharmaceutical, cosmetics, food, or FDA-regulated manufacturing industries.
• Fresh graduates are encouraged to apply.
• Knowledge of current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP), and FDA regulations is an advantage.
• Strong attention to detail and observation skills.
• Good communication, analytical, and organizational skills.
• Proficient in documentation and basic computer applications

II. Key Responsibilities

• Production line clearance and monitoring
• In-process inspection and quality monitoring
• Raw materials, packaging materials and finished product inspection
• Warehouse and good storage practice monitoring
• Documentation review and compliance verification
• FDA, cGMP and GLP compliance
• Deviation, non-conformance and CAPA support
• Product release support