393 Quality Control Analyst jobs in Kenya
Quality Control Analyst
Nairobi, Nairobi
KES180000 - KES360000 Y
Accurate Steel Mills Limited
Posted today
Job Viewed
Job Description
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
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0
Pharmaceutical Quality Control Analyst
30100 Garissa, North Eastern
KES75000 Monthly
WhatJobs
Posted 5 days ago
Job Viewed
Job Description
Our client, a rapidly growing pharmaceutical company, is looking for an experienced Pharmaceutical Quality Control Analyst to join their team in Garissa, Garissa, KE . This role is critical in ensuring the quality, safety, and efficacy of all manufactured pharmaceutical products. The successful candidate will perform a wide range of analytical tests on raw materials, in-process samples, and finished products using various laboratory techniques and equipment. Responsibilities include executing method validation protocols, maintaining accurate and detailed laboratory records, and adhering strictly to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). You will be expected to troubleshoot analytical methods, investigate out-of-specification (OOS) results, and collaborate with production and formulation teams to resolve quality issues. The analyst will also be involved in the stability testing programs, ensuring product shelf-life compliance. Proficiency in using analytical instrumentation such as HPLC, GC, UV-Vis spectrophotometers, and dissolution testers is essential. The ideal candidate will hold a Bachelor's degree in Pharmacy, Chemistry, Biochemistry, or a related life science discipline, coupled with a minimum of 3 years of hands-on experience in pharmaceutical quality control. A thorough understanding of pharmacopoeial standards (e.g., BP, USP, EP) and regulatory requirements within the pharmaceutical industry is mandatory. Excellent attention to detail, strong analytical and problem-solving abilities, and the capacity to work effectively under pressure are key attributes. The ability to work independently and as part of a collaborative team is also important. This position offers a competitive salary and benefits package, along with opportunities for professional growth within a reputable organization committed to advancing healthcare solutions. If you are a meticulous scientist dedicated to upholding the highest quality standards in pharmaceuticals, we invite you to submit your application.
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1
Pharmaceutical Quality Control Analyst
00202 Ongata Rongai, Rift Valley
KES100000 Annually
WhatJobs
Posted 11 days ago
Job Viewed
Job Description
Our client is seeking a meticulous and analytical Pharmaceutical Quality Control Analyst to join their team. This role offers a Hybrid work model, combining remote flexibility with essential on-site laboratory work. The ideal candidate will possess a strong background in pharmaceutical sciences, analytical chemistry, and quality assurance principles. You will be responsible for performing a wide range of laboratory tests on raw materials, in-process samples, and finished pharmaceutical products to ensure they meet stringent quality standards and regulatory requirements. This includes utilizing various analytical techniques and instrumentation such as HPLC, GC, spectroscopy, and wet chemistry methods. Key responsibilities involve the accurate execution of test methods, meticulous documentation of results, investigation of out-of-specification (OOS) results, and contribution to method validation activities. The Pharmaceutical Quality Control Analyst will play a vital role in upholding the integrity and safety of pharmaceutical products throughout their lifecycle. Strong attention to detail, excellent record-keeping skills, and a thorough understanding of Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) are essential for success in this role. The ability to collaborate effectively with cross-functional teams, both remotely and on-site, is also crucial.
Key Responsibilities:
Key Responsibilities:
- Perform analytical testing on raw materials, intermediate products, and finished pharmaceutical goods using various laboratory techniques and equipment.
- Conduct tests for identity, purity, strength, and quality according to established specifications and standard operating procedures (SOPs).
- Operate and maintain analytical instruments such as HPLC, GC, UV-Vis spectrophotometers, and dissolution apparatus.
- Accurately record and document all testing results, observations, and deviations in laboratory notebooks and LIMS.
- Investigate and troubleshoot out-of-specification (OOS) or out-of-trend (OOT) results, participating in root cause analysis.
- Assist in the validation and qualification of analytical methods and equipment.
- Ensure compliance with all relevant regulatory guidelines, including GMP, GLP, and ICH.
- Prepare and review quality control documentation, including test reports and certificates of analysis.
- Participate in internal and external audits as required.
- Collaborate with R&D, Production, and Regulatory Affairs departments to address quality-related issues.
- Maintain a safe and organized laboratory environment.
- Contribute to continuous improvement initiatives within the quality control department.
- Bachelor's degree in Chemistry, Pharmaceutical Sciences, Biochemistry, or a related scientific discipline.
- Minimum of 3-5 years of experience in pharmaceutical quality control or analytical laboratory setting.
- Hands-on experience with HPLC, GC, and other common analytical instrumentation.
- Thorough understanding of pharmaceutical quality systems, GMP, and GLP.
- Proficiency in data analysis and interpretation.
- Excellent laboratory notebook keeping and documentation skills.
- Strong problem-solving abilities and attention to detail.
- Good written and verbal communication skills.
- Ability to work effectively both independently and as part of a hybrid team.
- Familiarity with pharmacopoeias (e.g., USP, EP, BP) is advantageous.
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2
Pharmaceutical Quality Control Analyst
40100 Kisumu
KES100000 Annually
WhatJobs
Posted 13 days ago
Job Viewed
Job Description
Our client is seeking a meticulous and dedicated Pharmaceutical Quality Control Analyst to join their team in a fully remote capacity. This role is vital in ensuring the quality and safety of pharmaceutical products through rigorous testing and analysis. You will be responsible for performing a wide range of analytical tests on raw materials, in-process samples, and finished products according to established protocols and regulatory guidelines. This includes utilizing various laboratory techniques and instrumentation such as HPLC, GC, UV-Vis spectroscopy, and titration. You will meticulously document all testing procedures, results, and deviations in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). The role involves reviewing and approving analytical data, preparing Certificates of Analysis (CoAs), and troubleshooting analytical methods when necessary. You will also participate in method validation and transfer activities, and contribute to the investigation of out-of-specification (OOS) results. Maintaining laboratory equipment, ensuring proper calibration, and managing laboratory supplies will be part of your responsibilities. The ideal candidate will possess a Bachelor's or Master's degree in Pharmacy, Chemistry, Biochemistry, or a related life science field. A minimum of 3 years of experience in pharmaceutical quality control or quality assurance is required. Hands-on experience with analytical instrumentation and adherence to regulatory standards (e.g., ICH, FDA) are essential. Strong attention to detail, excellent organizational skills, and proficiency in data analysis and scientific documentation are paramount. As this is a remote role, you must be self-motivated, disciplined, and capable of managing your workload effectively without direct supervision. Excellent written and verbal communication skills are necessary for reporting and collaborating with team members. Join our forward-thinking pharmaceutical company and contribute to delivering high-quality medicines.
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3
Pharmaceutical Quality Control Analyst
41102 Kisumu
KES250000 Annually
WhatJobs
Posted 14 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is seeking a meticulous and experienced Pharmaceutical Quality Control Analyst to join their manufacturing facility. This position requires dedicated on-site presence to ensure the highest standards of quality in our pharmaceutical products. The successful candidate will be responsible for conducting a wide range of laboratory tests and analyses to ensure raw materials, in-process samples, and finished products meet stringent quality specifications and regulatory requirements. This role demands a strong understanding of analytical chemistry, Good Manufacturing Practices (GMP), and quality assurance principles within the pharmaceutical industry. The ideal candidate will possess excellent attention to detail, a systematic approach to work, and the ability to perform complex analytical procedures accurately and efficiently.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- 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.
Qualifications:
- 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.
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4
Quality Control Analyst (Pharmaceutical)
20300 Abothuguchi West
KES180000 Annually
WhatJobs
Posted 14 days ago
Job Viewed
Job Description
Our client is seeking a meticulous and detail-oriented Quality Control Analyst to join their pharmaceutical division. This role plays a crucial part in ensuring the safety, efficacy, and quality of our pharmaceutical products. The position offers a hybrid work model, combining remote flexibility with essential on-site laboratory work. The successful candidate will be responsible for performing a range of analytical tests and procedures according to established protocols and regulatory standards.
Responsibilities:
Responsibilities:
- 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.
This advertiser has chosen not to accept applicants from your region.
5
Pharmaceutical Quality Control Analyst
00200 Ongata Rongai, Rift Valley
KES70000 Annually
WhatJobs
Posted 14 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is seeking a meticulous and detail-oriented Pharmaceutical Quality Control Analyst to join their team. This role is crucial in ensuring the quality, safety, and efficacy of pharmaceutical products manufactured by our client. The successful candidate will be responsible for performing a wide range of analytical tests on raw materials, in-process samples, and finished products using various laboratory instruments and techniques. This includes, but is not limited to, High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), UV-Vis Spectrophotometry, and titration methods. You will meticulously document all test results, prepare Certificates of Analysis (CoAs), and maintain accurate laboratory records in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). Furthermore, you will be involved in method validation and transfer activities, ensuring that analytical procedures are robust and reliable. Identifying and investigating out-of-specification (OOS) results, deviations, and customer complaints will be a key responsibility, requiring strong problem-solving skills and a thorough understanding of pharmaceutical quality systems. You will also participate in internal and external audits and contribute to the continuous improvement of quality control processes. The ideal candidate will possess a Bachelor's or Master's degree in Chemistry, Pharmacy, or a related scientific field, coupled with significant hands-on experience in a pharmaceutical QC laboratory setting. Strong knowledge of analytical chemistry principles, instrumentation, and regulatory guidelines (e.g., FDA, EMA) is essential. Excellent written and verbal communication skills, along with strong organizational and time-management abilities, are required. This role offers a hybrid work arrangement, balancing essential on-site laboratory work with remote administrative and data analysis tasks. You will be expected to work collaboratively with R&D, manufacturing, and regulatory affairs teams to ensure product quality throughout the lifecycle. This position is based in **Ongata Rongai, Kajiado, KE**, and involves a combination of on-site and remote responsibilities.
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6
Pharmaceutical Quality Control Analyst
80200 Shella
KES120000 Annually
WhatJobs
Posted 14 days ago
Job Viewed
Job Description
Our client is seeking a meticulous and detail-oriented Pharmaceutical Quality Control Analyst to join their team. This role plays a critical part in ensuring the quality and safety of pharmaceutical products. You will be responsible for conducting a wide range of analytical tests on raw materials, in-process samples, and finished products using various laboratory instruments and methodologies. Accurate documentation and adherence to strict quality standards and regulatory guidelines are paramount.
Key Responsibilities:
Qualifications:
This position offers a hybrid work arrangement, combining essential on-site laboratory work with remote flexibility for data analysis and reporting.
Key Responsibilities:
- Perform routine and non-routine analytical testing of pharmaceutical materials using techniques such as HPLC, GC, UV-Vis, FTIR, and Karl Fischer titration.
- Prepare reagents, solutions, and standards required for testing.
- Document all testing procedures and results accurately and promptly in accordance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
- Analyze and interpret test data, comparing results against established specifications.
- Investigate out-of-specification (OOS) results and deviations, participating in root cause analysis.
- Calibrate and maintain laboratory equipment, ensuring proper functioning and performance.
- Participate in method validation and verification activities.
- Maintain a clean and organized laboratory environment.
- Assist in the preparation of Certificates of Analysis (CoA).
- Stay updated with relevant pharmacopoeial standards (e.g., USP, EP) and regulatory requirements.
Qualifications:
- Bachelor's degree in Chemistry, Pharmacy, Biotechnology, or a related scientific field.
- 1-3 years of experience in a pharmaceutical quality control laboratory setting.
- Hands-on experience with common analytical instruments (HPLC, GC, UV-Vis).
- Knowledge of GMP, GLP, and relevant regulatory guidelines.
- Strong analytical and problem-solving skills.
- Meticulous attention to detail and accuracy in data recording.
- Good written and verbal communication skills.
- Ability to work effectively both independently and as part of a team.
- Proficiency in using laboratory information management systems (LIMS) is a plus.
This position offers a hybrid work arrangement, combining essential on-site laboratory work with remote flexibility for data analysis and reporting.
This advertiser has chosen not to accept applicants from your region.
7
Pharmaceutical Quality Control Analyst
00200 Ongata Rongai, Rift Valley
KES75000 Annually
WhatJobs
Posted 14 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is looking for a meticulous and analytical Pharmaceutical Quality Control Analyst to join their team in **Ongata Rongai, Kajiado, KE**. This role is integral to ensuring the quality, safety, and efficacy of our pharmaceutical products. The successful candidate will perform a wide range of laboratory tests and analyses on raw materials, in-process samples, and finished products using sophisticated analytical techniques and equipment. Responsibilities include developing, validating, and implementing analytical methods, maintaining detailed and accurate laboratory records, and preparing comprehensive reports on test results. You will be expected to adhere strictly to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP), as well as relevant regulatory guidelines. Troubleshooting instrument malfunctions and identifying deviations from established specifications will be a key part of the role. Collaboration with research and development, production, and regulatory affairs teams will be essential to address quality issues and implement corrective actions. The ideal candidate will possess a strong understanding of pharmaceutical quality systems, a keen eye for detail, and the ability to work independently as well as part of a team. Proficiency in using analytical instruments such as HPLC, GC, UV-Vis spectrophotometers, and dissolution testers is required. A proactive approach to identifying potential quality risks and contributing to process improvements is highly valued. This position offers a dynamic work environment and the opportunity to contribute significantly to the pharmaceutical industry.
This advertiser has chosen not to accept applicants from your region.
8
Pharmaceutical Quality Control Analyst
80300 Shella
KES120000 Annually
WhatJobs
Posted 14 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is seeking a meticulous and dedicated Pharmaceutical Quality Control Analyst to join their esteemed team. This is an on-site position where you will play a critical role in ensuring the highest standards of quality for all manufactured pharmaceutical products. Your responsibilities will encompass performing a wide range of analytical tests, meticulously documenting results, and contributing to the overall quality assurance framework of the company.
The ideal candidate will possess a strong foundation in analytical chemistry and a comprehensive understanding of pharmaceutical quality control principles and regulatory requirements (e.g., GMP). You should be proficient in using various laboratory equipment, such as HPLC, GC, UV-Vis spectrophotometers, and titration apparatus. Excellent attention to detail, accuracy, and a commitment to maintaining a safe and compliant laboratory environment are paramount. You will be responsible for testing raw materials, in-process samples, and finished products against established specifications. The ability to interpret analytical data, troubleshoot laboratory issues, and contribute to method validation activities is essential. Strong record-keeping skills and the ability to work effectively within a team are also highly valued.
Key responsibilities include:
The ideal candidate will possess a strong foundation in analytical chemistry and a comprehensive understanding of pharmaceutical quality control principles and regulatory requirements (e.g., GMP). You should be proficient in using various laboratory equipment, such as HPLC, GC, UV-Vis spectrophotometers, and titration apparatus. Excellent attention to detail, accuracy, and a commitment to maintaining a safe and compliant laboratory environment are paramount. You will be responsible for testing raw materials, in-process samples, and finished products against established specifications. The ability to interpret analytical data, troubleshoot laboratory issues, and contribute to method validation activities is essential. Strong record-keeping skills and the ability to work effectively within a team are also highly valued.
Key responsibilities include:
- Performing analytical tests on raw materials, intermediate products, and finished pharmaceutical goods.
- Utilizing various analytical instruments (e.g., HPLC, GC, FTIR, UV-Vis) to conduct tests.
- Ensuring all testing is performed in accordance with established Standard Operating Procedures (SOPs) and regulatory guidelines.
- Accurately documenting all test results, observations, and deviations in laboratory notebooks and electronic systems.
- Investigating out-of-specification (OOS) results and participating in root cause analysis.
- Calibrating and maintaining laboratory equipment to ensure accurate performance.
- Participating in method validation and transfer activities.
- Preparing and standardizing reagents and solutions.
- Maintaining a clean, organized, and safe laboratory environment.
- Collaborating with production and quality assurance departments to resolve quality issues.
- Contributing to continuous improvement initiatives within the quality control laboratory.
This advertiser has chosen not to accept applicants from your region.
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