564 Quality Analyst jobs in Kenya
Remote Production Quality Analyst
00100 Njiru Village
KES75000 Annually
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Job Description
Our client is seeking a meticulous and analytical Remote Production Quality Analyst to ensure the highest standards in manufacturing processes and outputs. This fully remote role requires a keen eye for detail, a strong understanding of quality control methodologies, and the ability to analyze production data effectively. You will be responsible for reviewing production records, identifying deviations from quality standards, developing corrective actions, and contributing to continuous improvement initiatives. The ideal candidate will have experience in quality assurance within a manufacturing or production environment and proficiency in data analysis tools. Your role is vital in maintaining product integrity and operational excellence from a remote perspective.
Key Responsibilities:
Qualifications:
This is an excellent opportunity for a quality professional to contribute to manufacturing excellence through a remote role, impacting product quality and process improvement.
Key Responsibilities:
- Develop and implement quality control plans and procedures for production processes.
- Review production documentation, including batch records, test results, and inspection reports, for accuracy and compliance.
- Identify, document, and analyze non-conforming products or processes.
- Propose and implement corrective and preventive actions (CAPA) to address quality issues.
- Monitor key performance indicators (KPIs) related to production quality and efficiency.
- Conduct root cause analysis for quality failures and deviations.
- Collaborate with production, engineering, and R&D teams to resolve quality concerns.
- Stay updated on industry quality standards and regulatory requirements.
- Contribute to the development and improvement of quality management systems.
- Prepare quality reports and present findings to management.
Qualifications:
- Bachelor's degree in Engineering, Manufacturing Technology, Quality Management, or a related field, or equivalent practical experience.
- Minimum of 3 years of experience in quality assurance or quality control in a manufacturing or production setting.
- Solid understanding of quality management principles (e.g., ISO 9001, Six Sigma, Lean Manufacturing).
- Proficiency in data analysis, statistical process control (SPC), and quality tools.
- Experience with root cause analysis techniques (e.g., 5 Whys, Fishbone diagrams).
- Excellent attention to detail and accuracy.
- Strong analytical and problem-solving skills.
- Good written and verbal communication skills.
- Ability to work independently and manage time effectively in a remote environment.
- Familiarity with manufacturing execution systems (MES) or enterprise resource planning (ERP) systems is a plus.
This is an excellent opportunity for a quality professional to contribute to manufacturing excellence through a remote role, impacting product quality and process improvement.
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Remote Senior Sanitation Quality Analyst
00100 Mumbuni
KES80000 Annually
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Our client is seeking a highly motivated and experienced Remote Senior Sanitation Quality Analyst to join their dynamic team. This is a fully remote position, offering flexibility and the opportunity to contribute to maintaining the highest standards of hygiene and sanitation across diverse industries from the comfort of your home office. The ideal candidate will possess a strong understanding of sanitation protocols, quality assurance methodologies, and regulatory compliance.
Responsibilities:
Qualifications:
This role is critical in ensuring the safety and integrity of our client's operations. We are looking for a dedicated professional who is passionate about maintaining superior sanitation standards in a remote work environment.
Responsibilities:
- Develop, implement, and monitor sanitation quality assurance programs.
- Conduct remote audits and inspections of sanitation procedures and documentation.
- Analyze data related to sanitation effectiveness, identifying trends and areas for improvement.
- Provide expert guidance and training to teams on best practices in sanitation and hygiene.
- Ensure compliance with relevant health, safety, and environmental regulations.
- Collaborate with cross-functional teams to address sanitation challenges and implement corrective actions.
- Prepare detailed reports on sanitation quality performance and findings.
- Stay abreast of industry advancements and regulatory changes in sanitation and hygiene.
- Manage and maintain documentation related to sanitation procedures and compliance.
- Contribute to the continuous improvement of sanitation standards and protocols.
Qualifications:
- Bachelor's degree in Environmental Health, Public Health, Biology, Chemistry, or a related field.
- Minimum of 5 years of experience in sanitation, quality assurance, or a related role, preferably within a regulated industry.
- Proven experience in developing and implementing sanitation programs.
- In-depth knowledge of HACCP, GMP, and other relevant quality and food safety systems.
- Excellent analytical and problem-solving skills.
- Strong communication and interpersonal skills, with the ability to collaborate effectively with remote teams.
- Proficiency in data analysis software and Microsoft Office Suite.
- Ability to work independently and manage multiple priorities in a remote setting.
- Certification in relevant sanitation or quality assurance disciplines is a plus.
- Familiarity with remote auditing tools and technologies is advantageous.
This role is critical in ensuring the safety and integrity of our client's operations. We are looking for a dedicated professional who is passionate about maintaining superior sanitation standards in a remote work environment.
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Senior Remote Manufacturing Quality Analyst
90104 Mumbuni
KES90000 Annually
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Our client is seeking a meticulous and experienced Senior Remote Manufacturing Quality Analyst to join their production team. This fully remote role is dedicated to upholding and improving the quality standards of our manufactured products. You will be responsible for developing and implementing quality control procedures, analyzing production data, and identifying areas for improvement in the manufacturing process. Key responsibilities include conducting root cause analysis for quality defects, preparing quality reports, and collaborating with production and engineering teams to implement corrective actions. You will also be involved in ensuring compliance with industry standards and regulatory requirements. The ideal candidate will have a Bachelor's degree in Engineering, Manufacturing Technology, or a related field, with at least 5 years of experience in quality assurance or quality control within a manufacturing environment. Strong analytical skills, proficiency in statistical process control (SPC), and experience with quality management systems (e.g., ISO 9001) are essential. Knowledge of Lean Manufacturing or Six Sigma methodologies is highly preferred. This role demands excellent attention to detail, strong problem-solving abilities, and effective communication skills to liaise with remote teams. You must be self-driven, organized, and capable of working independently while meeting strict deadlines. If you are a seasoned quality professional looking for a remote opportunity to make a significant impact on product quality, we encourage you to apply.
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2
Remote Senior Sanitation Quality Analyst
20200 Kapsuser
KES230000 Annually
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Our client, a leader in providing advanced cleaning and sanitation solutions for commercial and industrial sectors, is seeking a meticulous and experienced Remote Senior Sanitation Quality Analyst. This position is entirely remote, allowing you to contribute your expertise from anywhere. You will be responsible for developing and implementing rigorous quality control standards and procedures to ensure the effectiveness and safety of our sanitation products and services. Your core responsibilities will include analyzing quality data, identifying trends and root causes of non-compliance, recommending corrective actions, and developing training materials for sanitation protocols. You will also conduct remote audits and assessments of client sites (via video conferencing and documentation review) to ensure adherence to quality standards and regulatory requirements. The ideal candidate will possess a Bachelor's degree in Chemistry, Environmental Science, Public Health, or a related field, with a minimum of 5 years of experience in quality assurance, sanitation, or a related field. Strong knowledge of cleaning chemicals, disinfection techniques, and relevant health and safety regulations is crucial. Excellent analytical, problem-solving, and documentation skills are required, as is the ability to work independently and manage multiple projects effectively in a remote setting. Familiarity with quality management systems (e.g., ISO 9001) and data analysis software is highly desirable. Join us in upholding the highest standards of cleanliness and public health through meticulous quality assurance.
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3
Pharmaceutical Quality Control Analyst
01002 Gathiruini
KES75000 month
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Our client, a leading pharmaceutical company, is seeking a meticulous and detail-oriented Pharmaceutical Quality Control Analyst to join their team in Mlolongo, Machakos, KE . This role is critical in ensuring the quality and safety of pharmaceutical products through rigorous testing and analysis. The ideal candidate will possess a strong foundation in pharmaceutical sciences, analytical chemistry, and regulatory compliance. Responsibilities include performing in-process and finished product testing using various analytical techniques (e.g., HPLC, GC, UV-Vis spectrophotometry), preparing and analyzing raw materials, intermediate products, and finished goods, documenting all testing procedures and results accurately in compliance with Good Manufacturing Practices (GMP), maintaining laboratory equipment and ensuring calibration, troubleshooting analytical methods, investigating out-of-specification (OOS) results, and contributing to the continuous improvement of quality control processes. You will work closely with production, R&D, and regulatory affairs departments to ensure product integrity and adherence to industry standards. A Bachelor's or Master's degree in Pharmacy, Chemistry, Biotechnology, or a related life science field, along with at least two years of experience in a pharmaceutical QC laboratory setting, is required. Familiarity with pharmacopeial methods (e.g., USP, EP) and a thorough understanding of GMP and quality management systems are essential. Excellent analytical skills, precision, and a commitment to upholding the highest standards of quality are paramount for success in this role.
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4
Pharmaceutical Quality Control Analyst
20117 Naivasha, Rift Valley
KES70000 Annually
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Our client, a leading pharmaceutical company, is looking for a meticulous and detail-oriented Pharmaceutical Quality Control Analyst to join their team in Naivasha, Nakuru, KE . This role is crucial for ensuring the quality and safety of our pharmaceutical products. The successful candidate will be responsible for performing a variety of laboratory tests on raw materials, in-process samples, and finished products according to established protocols and regulatory guidelines. You will operate and maintain sophisticated analytical instruments, including HPLC, GC, UV-Vis spectrophotometers, and titration equipment. Accurate documentation of all testing procedures, results, and deviations in laboratory notebooks and electronic systems is a key responsibility. The analyst will also participate in method validation activities, ensuring that analytical methods are accurate, precise, and reliable. You will conduct investigations into out-of-specification (OOS) results, identify root causes, and recommend corrective and preventive actions (CAPAs). Collaboration with the R&D and Production departments to address quality issues and support product development is essential. Maintaining a clean and safe laboratory environment, adhering to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP), is paramount. The ability to interpret data, generate reports, and present findings to management is required. We are seeking individuals with a strong understanding of pharmaceutical quality systems and regulatory requirements. This hybrid role offers a blend of laboratory work and data analysis, providing a stimulating and rewarding career path within the pharmaceutical industry. The ideal candidate will have a Bachelor's degree in Chemistry, Pharmacy, or a related life science discipline, with prior experience in a pharmaceutical QC laboratory setting. Proficiency in analytical techniques and a commitment to quality excellence are essential. Join us in ensuring the highest standards of quality for life-saving medications in Naivasha .
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5
Pharmaceutical Quality Control Analyst
00204 Gathiruini
KES60000 Annually
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Our client, a leading pharmaceutical company, is seeking a meticulous and experienced Pharmaceutical Quality Control Analyst for their facility in **Mlolongo, Machakos, KE**. This role is integral to ensuring the safety, efficacy, and quality of our pharmaceutical products. You will be responsible for performing a variety of analytical tests on raw materials, in-process samples, and finished products using advanced laboratory equipment. Key duties include operating analytical instruments such as HPLC, GC, UV-Vis spectrophotometers, and dissolution testers; meticulously documenting all test results; and adhering strictly to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). The ideal candidate will have a strong background in analytical chemistry and a thorough understanding of pharmaceutical quality control principles. Excellent attention to detail, a commitment to accuracy, and the ability to work effectively in a fast-paced laboratory environment are essential. You will play a crucial role in maintaining compliance with regulatory standards and contributing to the overall quality assurance of our products. Collaboration with R&D, production, and regulatory affairs departments will be part of your responsibilities. We are looking for a dedicated professional with a passion for pharmaceutical sciences and a commitment to upholding the highest standards of quality and safety.
Key Responsibilities:
Key Responsibilities:
- Perform analytical tests on raw materials, intermediates, and finished products.
- Operate and maintain laboratory equipment (HPLC, GC, UV-Vis, etc.).
- Document test results accurately and maintain laboratory notebooks.
- Ensure compliance with GLP, GMP, and relevant regulatory guidelines.
- Analyze and interpret test data, preparing analytical reports.
- Participate in method validation and qualification activities.
- Investigate out-of-specification (OOS) results.
- Collaborate with cross-functional teams to resolve quality issues.
- Bachelor's degree in Pharmacy, Chemistry, Biotechnology, or a related life science field.
- Proven experience in pharmaceutical quality control laboratory.
- Hands-on experience with analytical instruments and methods.
- Knowledge of GMP, GLP, and regulatory requirements.
- Strong analytical, problem-solving, and critical thinking skills.
- Excellent attention to detail and documentation practices.
- Ability to work independently and as part of a team.
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Pharmaceutical Quality Control Analyst
20100 Mwembe
KES180000 Annually
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Job Description
Our client, a reputable pharmaceutical company, is seeking a meticulous and experienced Pharmaceutical Quality Control Analyst to join their team. This is a fully remote role, requiring a dedicated professional to perform essential quality checks and analyses on pharmaceutical products and raw materials from a distance. You will be responsible for ensuring that all products meet stringent quality standards and regulatory requirements, contributing to the safety and efficacy of our medications. The ideal candidate will possess a strong scientific background and a keen eye for detail.
Key Responsibilities:
Key Responsibilities:
- Perform analytical testing on raw materials, in-process samples, and finished pharmaceutical products using various laboratory techniques (e.g., HPLC, GC, UV-Vis spectroscopy, Karl Fischer titration).
- Develop, validate, and transfer analytical methods according to regulatory guidelines (e.g., ICH, FDA, EMA).
- Prepare and review analytical reports, ensuring accuracy and completeness of data.
- Maintain laboratory equipment and instruments, ensuring calibration and proper functioning.
- Document all experimental procedures, results, and observations in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
- Investigate out-of-specification (OOS) results and deviations, recommending and implementing corrective and preventive actions (CAPAs).
- Conduct stability studies for pharmaceutical products and analyze the results.
- Review and approve batch records and analytical documentation.
- Collaborate with R&D, manufacturing, and regulatory affairs departments to resolve quality issues.
- Stay updated on the latest advancements in analytical techniques and regulatory requirements.
- Participate in internal and external audits as required.
- Ensure the safe handling and disposal of chemicals and laboratory waste.
- Bachelor's or Master's degree in Chemistry, Pharmacy, Pharmaceutical Sciences, or a related discipline.
- Minimum of 3-5 years of hands-on experience in pharmaceutical quality control or assurance.
- Proficiency in various analytical techniques commonly used in the pharmaceutical industry (HPLC, GC, AAS, IR, UV-Vis).
- Strong understanding of GMP, GLP, and relevant regulatory guidelines (ICH, FDA, EMA).
- Excellent data analysis, interpretation, and documentation skills.
- Proficiency in laboratory information management systems (LIMS) and electronic lab notebooks (ELN).
- Strong problem-solving skills and the ability to work independently.
- Excellent written and verbal communication skills.
- Ability to manage multiple projects and prioritize tasks effectively in a remote work environment.
- Attention to detail and a commitment to accuracy.
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7
Pharmaceutical Quality Control Analyst
00300 Kakamega, Western
KES78000 Annually
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Posted 1 day ago
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Job Description
Our client is seeking a meticulous and experienced Pharmaceutical Quality Control Analyst to join their esteemed team. This hybrid role requires a keen eye for detail and a strong understanding of pharmaceutical manufacturing processes and regulatory standards. You will be responsible for conducting a wide range of tests on raw materials, in-process samples, and finished products to ensure they meet stringent quality specifications and comply with Good Manufacturing Practices (GMP). Your duties will include performing physical, chemical, and microbiological analyses using various laboratory techniques and sophisticated instrumentation. Accurate record-keeping and meticulous documentation of all testing procedures and results are paramount.
The successful candidate will work collaboratively with the Quality Assurance department to identify and address any deviations from quality standards. You will also be involved in method validation, stability testing, and the investigation of out-of-specification results. This position requires a strong foundation in analytical chemistry, pharmaceutics, and relevant regulatory guidelines (e.g., FDA, WHO). The ability to troubleshoot laboratory equipment and analytical methods is essential. You will contribute to maintaining the highest standards of product quality and safety, ensuring that all pharmaceutical products are safe and effective for patient use. This role offers a blend of laboratory-based work and opportunities for contribution to quality system improvements. A proactive approach to identifying potential quality risks and contributing to risk mitigation strategies will be highly valued. Continuous learning and staying updated with the latest advancements in pharmaceutical quality control methodologies are crucial. You will play a vital role in upholding the company's commitment to excellence and regulatory compliance within the pharmaceutical industry.
Responsibilities:
Qualifications:
The successful candidate will work collaboratively with the Quality Assurance department to identify and address any deviations from quality standards. You will also be involved in method validation, stability testing, and the investigation of out-of-specification results. This position requires a strong foundation in analytical chemistry, pharmaceutics, and relevant regulatory guidelines (e.g., FDA, WHO). The ability to troubleshoot laboratory equipment and analytical methods is essential. You will contribute to maintaining the highest standards of product quality and safety, ensuring that all pharmaceutical products are safe and effective for patient use. This role offers a blend of laboratory-based work and opportunities for contribution to quality system improvements. A proactive approach to identifying potential quality risks and contributing to risk mitigation strategies will be highly valued. Continuous learning and staying updated with the latest advancements in pharmaceutical quality control methodologies are crucial. You will play a vital role in upholding the company's commitment to excellence and regulatory compliance within the pharmaceutical industry.
Responsibilities:
- Perform quality control testing on raw materials, intermediates, and finished pharmaceutical products.
- Conduct assays using various analytical techniques such as HPLC, GC, UV-Vis, and Karl Fischer titration.
- Document all laboratory activities, results, and deviations accurately in compliance with cGMP.
- Prepare reagents and maintain laboratory equipment in good working order.
- Participate in method validation and transfer activities.
- Investigate out-of-specification (OOS) results and identify root causes.
- Ensure compliance with all relevant regulatory guidelines and internal SOPs.
- Contribute to the continuous improvement of quality control processes.
- Collaborate with production and quality assurance teams on quality-related matters.
- Maintain a safe and organized laboratory environment.
Qualifications:
- Bachelor's degree in Pharmacy, Chemistry, Microbiology, or a related science field.
- Minimum 3 years of experience in pharmaceutical quality control or assurance.
- Proficiency in analytical instrumentation (HPLC, GC, Spectrophotometry).
- Knowledge of cGMP, ICH guidelines, and pharmaceutical regulatory requirements.
- Strong understanding of laboratory techniques and data analysis.
- Excellent documentation and record-keeping skills.
- Ability to work effectively in a team and independently.
- Problem-solving and critical thinking abilities.
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