6,417 Remote Quality Assurance Specialist Sanitation Standards jobs in Kenya

• Develop, refine, and implement robust quality assurance programs and standard operating procedures (SOPs) for cleaning and sanitation services.
• Conduct remote assessments and audits of cleaning quality through photographic evidence, video submissions, and detailed reporting from on-site personnel.
• Analyze inspection data and performance metrics to identify areas for improvement and implement corrective action plans.
• Train and guide on-site cleaning teams on best practices, new techniques, and adherence to quality standards via virtual platforms.
• Stay updated on industry trends, regulations (e.g., HACCP, WHO guidelines), and emerging technologies in cleaning and sanitation.
• Collaborate with operations managers and regional supervisors to ensure consistent application of quality standards across all locations.
• Develop and maintain detailed quality control documentation, checklists, and reporting templates.
• Investigate and resolve quality-related complaints or issues reported by stakeholders or clients.
• Monitor the effectiveness of cleaning products, equipment, and methodologies, recommending upgrades or changes as needed.
• Prepare regular quality performance reports for senior management, highlighting key findings and improvement initiatives.
• Foster a culture of continuous improvement and excellence in sanitation services.
• Ensure compliance with health, safety, and environmental regulations related to cleaning operations.

• Bachelor's degree in Environmental Health, Public Health, Hospitality Management, or a related field.
• A minimum of 7 years of progressive experience in quality assurance, quality control, or operations management within the cleaning, sanitation, or hospitality industry.
• Proven experience in developing and implementing quality management systems.
• Strong knowledge of cleaning science, disinfection protocols, and relevant health and safety regulations.
• Excellent analytical and problem-solving skills, with a keen attention to detail.
• Proficiency in using digital tools for remote auditing, data analysis, and reporting (e.g., MS Office Suite, specialized QA software, communication platforms).
• Strong communication and interpersonal skills, with the ability to provide clear and constructive feedback remotely.
• Experience in training and mentoring teams virtually.
• Ability to work independently and manage multiple tasks effectively in a remote setting.
• Proactive approach to identifying and addressing potential quality issues.
• Certification in a relevant field (e.g., Certified Infection Control Professional) is an advantage.

• Develop, implement, and maintain comprehensive Quality Assurance (QA) and Quality Control (QC) systems.
• Oversee the execution of analytical testing for raw materials, in-process samples, and finished products.
• Ensure compliance with cGMP, ICH guidelines, and other relevant regulatory standards.
• Write, review, and approve Standard Operating Procedures (SOPs), batch records, and validation protocols.
• Manage deviations, Out-of-Specification (OOS) results, and CAPA investigations.
• Conduct internal audits and support external regulatory inspections.
• Train and mentor QA/QC personnel.
• Analyze quality data to identify trends and implement continuous improvement initiatives.
• Collaborate with R&D, manufacturing, and regulatory affairs teams to ensure product quality and compliance.
• Stay current with evolving regulatory requirements and industry best practices in pharmaceutical quality management.

• Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific discipline. M.Sc. or Ph.D. is a plus.
• Minimum of 7 years of progressive experience in pharmaceutical Quality Assurance and/or Quality Control.
• In-depth knowledge of cGMP regulations, ICH guidelines, and pharmaceutical manufacturing processes.
• Proven experience in managing analytical testing, method validation, and stability studies.
• Strong understanding of quality management systems, including deviation management, CAPA, and change control.
• Excellent documentation, analytical, and problem-solving skills.
• Strong leadership and team management capabilities.
• Exceptional communication and interpersonal skills, with the ability to collaborate effectively in a remote setting.
• Experience with electronic quality management systems (eQMS) is beneficial.
• Detail-oriented with a strong commitment to quality and compliance.

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Job Description
We're committed to bringing passion and customer focus to the business.

If you like wild growth and working with happy, enthusiastic over-achievers, you'll enjoy your career with us.

• Develop, implement, and manage comprehensive Quality Assurance (QA) programs for pharmaceutical products and processes.
• Ensure compliance with Good Manufacturing Practices (GMP), Good Distribution Practices (GDP), and other relevant regulatory guidelines (e.g., FDA, EMA).
• Conduct internal and external audits of manufacturing sites, suppliers, and contract manufacturers.
• Review and approve batch records, validation protocols, and other critical quality documentation.
• Investigate deviations, out-of-specifications (OOS) results, and customer complaints, implementing corrective and preventive actions (CAPA).
• Develop and maintain the company's Quality Management System (QMS), including SOPs, work instructions, and quality agreements.
• Provide training to personnel on QA principles, GMP, and regulatory requirements.
• Collaborate with R&D, manufacturing, and regulatory affairs departments to ensure product quality throughout the lifecycle.
• Manage the release of finished pharmaceutical products.
• Stay current with evolving regulatory landscapes and industry best practices.
• Lead quality improvement initiatives and contribute to the continuous enhancement of quality systems.
• Prepare for and host regulatory inspections.

• Master's degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Biotechnology, or a related scientific field.
• A minimum of 8 years of experience in Pharmaceutical Quality Assurance and Quality Control, with a strong focus on GMP compliance.
• In-depth knowledge of pharmaceutical manufacturing processes, analytical testing, and stability studies.
• Proven experience in conducting audits and managing CAPA systems.
• Familiarity with global regulatory requirements and submission processes.
• Excellent understanding of quality risk management principles.
• Strong analytical, problem-solving, and decision-making skills.
• Exceptional written and verbal communication skills, with the ability to present complex information clearly and concisely.
• Demonstrated leadership capabilities and the ability to manage projects and teams remotely.
• Proficiency in using quality management software and standard office applications.
• Relevant professional certifications (e.g., ASQ CQA) are a plus.

• Develop and maintain pharmaceutical quality assurance systems and SOPs.
• Ensure compliance with GMP, GDP, and other relevant pharmaceutical regulations.
• Lead internal and external audits, including supplier audits.
• Manage deviation investigations, CAPA implementation, and change control processes.
• Analyze quality data, identify trends, and implement corrective and preventive actions.
• Oversee risk management activities related to product quality.
• Train staff on quality assurance procedures and regulatory requirements.
• Collaborate with manufacturing, R&D, and regulatory affairs teams.
• Champion a strong quality culture throughout the organization.

• Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science discipline.
• Advanced degree or relevant certifications (e.g., ASQ CQA) are a plus.
• Minimum of 10 years of experience in pharmaceutical quality assurance.
• In-depth knowledge of GMP, GDP, ICH guidelines, and regulatory submission processes.
• Proven experience in conducting audits, managing deviations, and implementing CAPAs.
• Strong analytical and problem-solving skills.
• Excellent leadership, communication, and interpersonal skills.
• Ability to interpret complex regulatory requirements and drive compliance.
• Experience leading quality initiatives in a remote environment.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field.
• Minimum of 5 years of experience in pharmaceutical quality assurance or quality control.
• In-depth knowledge of GMP regulations (e.g., FDA, EMA) and quality management systems.
• Proven experience in batch record review, deviation investigation, and CAPA management.
• Experience with internal and external audits, including preparation for regulatory inspections.
• Strong understanding of pharmaceutical manufacturing processes and analytical testing.
• Excellent analytical, problem-solving, and critical thinking skills.
• Demonstrated ability to work independently and manage time effectively in a remote setting.
• Exceptional attention to detail and commitment to accuracy.
• Strong written and verbal communication skills.
• Familiarity with quality risk management principles.

• Develop, implement, and maintain Quality Management Systems (QMS).
• Ensure compliance with GMP, GLP, and other relevant pharmaceutical regulations.
• Review and approve batch manufacturing records and associated documentation.
• Investigate deviations, OOS results, and customer complaints, implementing CAPA plans.
• Conduct internal audits and support external regulatory inspections.
• Collaborate with R&D, manufacturing, and regulatory affairs teams on quality-related matters.
• Develop and deliver training programs on quality standards and procedures.
• Monitor and analyze quality metrics to identify trends and areas for improvement.
• Participate in supplier qualification and quality agreements.
• Maintain accurate and organized quality records.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field.
• Minimum of 5 years of experience in pharmaceutical quality assurance or quality control.
• In-depth knowledge of GMP, GLP, ICH guidelines, and other relevant regulatory standards.
• Experience with QMS, CAPA, deviation management, and change control processes.
• Proficiency in quality management software and statistical analysis tools.
• Strong analytical, problem-solving, and critical thinking skills.
• Excellent documentation and communication skills.
• Ability to work independently, manage priorities, and meet deadlines in a remote environment.
• Detail-oriented with a strong commitment to quality and compliance.