67 Testing jobs in Kenya
Quality Assurance Supervisor
Posted 27 days ago
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Senior Quality Assurance Engineer
Posted today
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Key Responsibilities:
- Develop and execute comprehensive quality assurance plans and test strategies for manufacturing processes.
- Lead and mentor a team of QA technicians in conducting rigorous product testing and inspections.
- Analyze production data and quality metrics to identify trends, root causes of defects, and areas for improvement.
- Implement and maintain quality control systems and procedures to ensure compliance with industry standards.
- Collaborate with engineering and production teams to resolve quality issues and implement corrective actions.
- Conduct audits of manufacturing processes and supplier quality to ensure adherence to standards.
- Stay updated on the latest advancements in quality assurance and manufacturing technologies.
- Prepare detailed reports on quality performance and recommend improvements.
- Bachelor's degree in Engineering, Manufacturing Technology, or a related field.
- Minimum 5 years of experience in quality assurance within the manufacturing sector.
- Proven experience in leading and managing QA teams.
- In-depth knowledge of quality management systems (e.g., ISO 9001).
- Familiarity with statistical process control (SPC) and other quality tools.
- Strong analytical, problem-solving, and decision-making skills.
- Excellent communication and collaboration abilities in a remote setting.
- Certification in Six Sigma or Lean Manufacturing is a plus.
Lead Quality Assurance Engineer
Posted today
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Quality Assurance (QA) Analyst
Posted 15 days ago
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Remote Pharmaceutical Quality Assurance Specialist
Posted today
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Key Responsibilities:
- Develop, implement, and maintain the Quality Management System (QMS) in compliance with regulatory requirements.
- Conduct internal and external audits of manufacturing sites, suppliers, and laboratories to assess compliance with GMP, GLP, and other standards.
- Review and approve quality-related documents, including batch records, validation protocols, and change controls.
- Investigate deviations, out-of-specification results, and customer complaints, implementing corrective and preventive actions (CAPA).
- Prepare and review documentation for regulatory submissions and inspections.
- Monitor and analyze quality metrics, identifying trends and areas for continuous improvement.
- Collaborate with cross-functional teams, including R&D, Manufacturing, and Regulatory Affairs, to ensure quality is integrated into all processes.
- Provide training to personnel on quality systems, GMP, and other relevant topics.
- Stay current with pharmaceutical regulations and industry best practices.
- Participate in quality risk assessments and manage risk mitigation strategies.
Qualifications:
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
- Minimum of 5 years of experience in pharmaceutical quality assurance or quality control.
- In-depth knowledge of GMP, GLP, GDP, and other relevant pharmaceutical quality standards.
- Experience with regulatory filings and inspections (e.g., FDA, EMA).
- Strong understanding of pharmaceutical manufacturing processes.
- Excellent analytical, problem-solving, and documentation skills.
- Proficiency in quality management software and standard office applications.
- Ability to work independently, manage time effectively, and meet deadlines in a remote setting.
- Strong communication and interpersonal skills for collaboration with diverse teams.
- Detail-oriented with a commitment to accuracy and compliance.
Remote Pharmaceutical Quality Assurance Specialist
Posted today
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Key Responsibilities:
- Review and approve manufacturing batch records, analytical test results, and other quality-related documents.
- Investigate deviations, out-of-specification (OOS) results, and customer complaints, implementing corrective and preventive actions (CAPA).
- Manage and maintain the change control system, ensuring all changes are properly documented and assessed for impact.
- Participate in internal and external audits (e.g., regulatory inspections, customer audits) and ensure timely closure of audit findings.
- Develop, review, and update Standard Operating Procedures (SOPs) and other quality system documents.
- Conduct risk assessments and implement strategies to mitigate quality risks.
- Monitor and analyze quality metrics and trends to identify areas for continuous improvement.
- Ensure compliance with all applicable regulatory requirements (e.g., FDA, EMA, local health authorities).
- Collaborate with R&D, Manufacturing, and Regulatory Affairs departments to ensure quality throughout the product lifecycle.
- Maintain accurate and organized quality records.
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field.
- Minimum of 4 years of experience in Quality Assurance or Quality Control within the pharmaceutical industry.
- In-depth knowledge of GMP, GLP, and ICH guidelines.
- Experience with quality management systems, including deviation investigations, change control, and CAPA.
- Strong analytical skills and attention to detail.
- Excellent written and verbal communication skills, with the ability to document findings clearly and concisely.
- Proficiency in Microsoft Office Suite and quality management software.
- Ability to work independently, manage priorities, and meet deadlines in a remote setting.
- Must have a reliable high-speed internet connection and a dedicated home office environment.
Remote Pharmaceutical Quality Assurance Specialist
Posted today
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Remote Pharmaceutical Quality Assurance Specialist
Posted today
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Responsibilities:
- Review and approve pharmaceutical documentation, including batch records and SOPs.
- Investigate deviations, out-of-specification results, and customer complaints.
- Ensure compliance with Good Manufacturing Practices (GMP) and other relevant regulations.
- Participate in internal and external audits and inspections.
- Develop, implement, and maintain quality control procedures.
- Conduct risk assessments and implement mitigation strategies.
- Manage change control processes for pharmaceutical products and processes.
- Prepare and review quality-related reports and documentation.
- Support validation activities for equipment, processes, and systems.
- Promote a quality-focused culture throughout the organization.
- Proven experience in Pharmaceutical Quality Assurance or Quality Control.
- In-depth knowledge of GMP, ICH guidelines, and regulatory requirements.
- Experience with quality management systems (QMS) and CAPA systems.
- Strong analytical and problem-solving skills.
- Proficiency in documentation review and investigation procedures.
- Excellent written and verbal communication skills.
- Ability to work independently and manage multiple priorities.
- Experience with validation processes is a plus.
- Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science field.
Senior Pharmaceutical Quality Assurance Manager
Posted today
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Key Responsibilities:
- Develop, implement, and maintain the company's Quality Management System (QMS).
- Ensure compliance with all relevant pharmaceutical regulations (e.g., cGMP, ICH guidelines).
- Oversee and manage quality control testing and release processes.
- Conduct internal audits and support external regulatory inspections.
- Manage deviation investigations, CAPA implementation, and change control processes.
- Review and approve batch records, validation protocols, and other critical documentation.
- Provide training and guidance to quality assurance personnel and other staff on quality-related matters.
- Collaborate with R&D, manufacturing, and regulatory affairs teams to ensure product quality.
- Monitor and analyze quality metrics and provide reports to senior management.
- Drive continuous improvement initiatives to enhance product quality and process efficiency.
Senior Pharmaceutical Quality Assurance Manager
Posted today
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Job Description
Responsibilities:
- Develop and implement comprehensive pharmaceutical quality assurance programs.
- Ensure compliance with GMP, GDP, ICH guidelines, and other relevant regulations.
- Conduct internal and external quality audits of manufacturing sites and suppliers.
- Manage deviation investigations, root cause analysis, and CAPA implementation.
- Oversee batch record review, release, and stability testing processes.
- Review and approve validation protocols and reports for equipment and processes.
- Manage change control procedures and ensure effective implementation of changes.
- Train and mentor QA personnel, fostering a strong quality culture.
- Liaise with regulatory agencies during inspections and inquiries.
- Drive continuous improvement initiatives within the quality system.
- Master's degree in Pharmacy, Pharmaceutical Sciences, Chemistry, or a related field.
- Minimum of 10 years of experience in pharmaceutical quality assurance and quality control.
- Extensive knowledge of GMP, GDP, ICH guidelines, and regulatory affairs.
- Proven experience in managing quality systems, audits, and regulatory inspections.
- Strong understanding of pharmaceutical manufacturing processes and analytical methods.
- Excellent leadership, communication, and problem-solving skills.
- Proficiency in quality management software and regulatory compliance tools.
- Ability to work independently and manage multiple priorities in a remote setting.
- Commitment to upholding the highest standards of pharmaceutical quality.