On-site Quality Chemist: GMP/GLP, Data & Compliance

Kimiki Solutions Incorporated; Cavite City; On-site; PHP 300,000 - 420,000; Full time

Benefits offered by this job

HMO

Hazardous Materials handling

Job summary

Kimiki Solutions Incorporated in Cavite on-site seeks a Quality Assurance Specialist with 1-3 years of experience in data analysis, quality systems, and regulatory compliance. You will develop and maintain GMP/GLP-compliant SOPs, procedures, and documentation.

Responsibilities include conducting quality audits, CAPA, method validation support, regulatory inspections, and cross-department collaboration to ensure product integrity.

Qualifications

• Bachelor’s degree in Chemistry or related science.
• Registered Chemist or Registered Chemical Engineer license required.
• 1–3 years of data analysis or quality systems experience in regulated industry.

Responsibilities

• Develop and maintain laboratory quality systems, SOPs, and procedures in GMP/GLP regulatory compliance.
• Monitor laboratory processes and conduct quality audits to ensure compliance.
• Data Analysis & Reporting: analyze laboratory data to assess quality and compliance with specifications.
• Prepare technical reports and assist in root cause analysis and CAPA for quality issues.
• Method Validation & Qualification: assist in validation, verification, and qualification of analytical methods.
• Regulatory & Compliance Support: ensure activities comply with FDA/EMA/ISO requirements and support inspections.

Skills

Analytical skills

Organizational skills

Communication skills

Time management

Prioritization

Education

Bachelor’s Degree in Chemistry

Registered Chemist license

Registered Chemical Engineer license

Job description

Kimiki Solutions Incorporated in Cavite on-site seeks a Quality Assurance Specialist with 1-3 years of experience in data analysis, quality systems, and regulatory compliance. You will develop and maintain GMP/GLP-compliant SOPs, procedures, and documentation.

Responsibilities include conducting quality audits, CAPA, method validation support, regulatory inspections, and cross-department collaboration to ensure product integrity.