1,610 Quality Analyst jobs in Kenya

Conduct routine quality checks on raw materials, in-process products, and finished goods to ensure compliance with specifications.

Develop, implement, and maintain quality assurance protocols, documentation, and reporting systems.

Monitor manufacturing processes to identify deviations and recommend corrective actions.

Support root cause analysis and corrective & preventive action (CAPA) initiatives for quality-related issues.

Collaborate with production, R&D, and supply chain teams to maintain quality across the value chain.

Ensure compliance with local and international food safety and quality standards (ISO, HACCP, GMP, etc.).

Prepare and present quality performance reports and recommend process improvements.

Train and sensitize staff on quality standards, procedures, and best practices.

Participate in internal and external audits, ensuring all documentation is up-to-date and accessible.

Proactively identify opportunities for quality improvement and operational efficiency.

Bachelor’s degree in Food Science, Industrial Chemistry, Quality Management, or a related field.

2–4 years of experience in a quality assurance role within the FMCG or manufacturing industry.

Strong knowledge of ISO standards, HACCP, GMP, and regulatory requirements.

Experience with laboratory testing methods, data analysis, and statistical quality control.

Proficiency in QA/QC tools, documentation, and reporting systems.

Strong problem-solving skills and keen attention to detail.

Excellent communication, teamwork, and analytical skills.

Company Description

Accurate Steel Mills Limited, a leader in steel manufacturing, produces a range of steel products for the construction and fabrication industries. Our commitment to excellence over the past decade has distinguished our products in the market and fostered long-lasting customer relationships. With a vision to become East Africa's most reliable and trusted steel manufacturer, we provide superior quality steel products. Our mission is to drive economic growth safely across Africa by offering consistently dependable products that meet rigorous mechanical and chemical testing standards.

Role Description

This is a full-time on-site role for a Quality Control Analyst located in Nairobi County, Kenya. The Quality Control Analyst will be responsible for conducting quality control tests, ensuring products meet standards, handling laboratory equipment, and maintaining quality assurance protocols. The analyst will perform daily inspections, analyze data, and prepare reports to ensure that the highest quality standards are met throughout the production process.

Qualifications

• Strong Analytical Skills
• Experience in Quality Control and Quality Assurance
• Proficiency in Laboratory Skills and handling Laboratory Equipment
• Attention to detail and a methodical approach to work
• Understanding of safety protocols and regulatory standards
• Excellent communication and documentation skills
• Bachelor's degree in Chemistry, Engineering, or related field
• Previous experience in steel manufacturing or related industry is a plus

• Perform analytical testing on raw materials, intermediates, finished products, and packaging materials using various laboratory techniques (e.g., HPLC, GC, UV-Vis Spectroscopy, Titration).
• Ensure all testing is conducted in compliance with established Standard Operating Procedures (SOPs), GMP, and relevant regulatory guidelines (e.g., FDA, EMA).
• Prepare reagents, standards, and samples for analytical testing.
• Calibrate and maintain laboratory equipment, ensuring it is in proper working order and records are meticulously kept.
• Document all test results, observations, and deviations accurately and in a timely manner in laboratory notebooks and electronic systems.
• Investigate out-of-specification (OOS) results and deviations, identifying root causes and recommending corrective and preventive actions (CAPAs).
• Participate in method validation and verification activities as required.
• Contribute to the review and improvement of SOPs and quality control procedures.
• Collaborate with other departments, such as Production, R&D, and Quality Assurance, to resolve quality-related issues.
• Maintain a clean and safe laboratory environment.

• A Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science discipline.
• Minimum of 3-5 years of experience in a Pharmaceutical Quality Control laboratory setting.
• Hands-on experience with analytical instrumentation commonly used in pharmaceutical QC (e.g., HPLC, GC, FTIR, UV-Vis, dissolution apparatus).
• Solid understanding of GMP, GLP, and pharmaceutical quality systems.
• Proficiency in performing analytical method validation and OOS investigations.
• Excellent laboratory technique, attention to detail, and data integrity.
• Strong documentation skills and the ability to maintain accurate records.
• Good problem-solving and critical-thinking abilities.
• Ability to work independently and as part of a team.
• Familiarity with relevant pharmacopeias (e.g., USP, EP, BP) is a plus.

• Conduct routine and non-routine analytical testing of raw materials, in-process samples, and finished pharmaceutical products using various analytical techniques (e.g., HPLC, GC, UV-Vis Spectroscopy, Titration).
• Prepare reagents, solutions, and standards required for testing.
• Maintain accurate and detailed laboratory records, documenting all procedures, results, and observations in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
• Calibrate and maintain laboratory equipment, ensuring proper functioning and adherence to calibration schedules.
• Investigate out-of-specification (OOS) results, identify root causes, and participate in deviation investigations.
• Assist in the validation and transfer of analytical methods.
• Review and approve testing data and reports.
• Stay informed about current pharmacopeial methods (e.g., USP, BP, EP) and relevant regulatory guidelines.
• Participate in internal and external audits as required.
• Contribute to the continuous improvement of quality control processes and procedures.

• Bachelor's degree in Chemistry, Biochemistry, Pharmacy, or a related scientific field.
• Minimum of 3 years of experience in a pharmaceutical quality control or analytical laboratory setting.
• Proficiency in operating and maintaining analytical instrumentation, particularly HPLC and GC.
• Solid understanding of GMP, GLP, and relevant regulatory requirements.
• Experience with pharmacopeial testing and monographs.
• Strong problem-solving skills and ability to troubleshoot analytical issues.
• Excellent attention to detail and accuracy in data recording and analysis.
• Good organizational and time management skills.
• Effective written and verbal communication abilities.
• Ability to work independently and collaboratively in a hybrid environment, balancing remote tasks with essential on-site laboratory duties.