Chemist

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

On-site - Cavite 1-3 Yrs Exp Bachelor Full-time

Job Description

• Quality Systems Management
• Develop and maintain laboratory quality systems, SOPs, and procedures in compliance with GMP, GLP, and regulatory requirements.
• Monitor laboratory processes and conduct quality audits to ensure compliance.
• Data Analysis & Reporting
• Analyze laboratory and product testing 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 the validation, verification, and qualification of analytical methods.
• Ensure proper documentation and compliance with regulatory standards.
• Regulatory & Compliance Support
• Ensure laboratory activities comply with applicable FDA, EMA, ISO, and other regulatory requirements.
• Support regulatory inspections, audits, and quality-related investigations.
• Collaborate with other departments to address quality and product integrity concerns.
• Identify and implement improvements in laboratory processes, efficiency, and quality systems.
• Train laboratory staff on quality procedures and best practices.
• Develop, improve, and reformulate products based on research, customer needs, and industry trends.
• Conduct R&D activities to support product innovation, troubleshooting, and optimization.

Qualifications:

• Education: Bachelor’s Degree in Chemistry or a related science/technical discipline.
• Licensure: Must possess a valid Registered Chemist license or Registered Chemical Engineer license
• Experience: 1-3 years experience in data analysis, quality systems, or a related field, preferably in a regulated industry.

Skills:

• Strong analytical and problem-solving abilities.
• Excellent organizational and time management skills.
• Strong communication (written and verbal) and interpersonal skills.
• Ability to manage multiple priorities and meet deadlines.

Insurance Health & Wellness

HMO

Chemicals and Hazardous Materials Management