15 Quality Management jobs in Nairobi
Quality Control Supervisor
Posted 2 days ago
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Job Description
- Establishing and overseeing comprehensive quality control protocols and standard operating procedures (SOPs).
- Conducting regular remote audits and inspections of production processes, materials, and finished goods.
- Analyzing quality data to identify trends, root causes of defects, and opportunities for process improvement.
- Developing and implementing corrective and preventive actions (CAPA) to address quality issues.
- Ensuring compliance with relevant industry standards, certifications, and regulatory requirements.
- Training and guiding production teams on quality standards and best practices.
- Managing the quality control team, including performance reviews and professional development.
- Collaborating with R&D, production, and supply chain teams to integrate quality into product development and material sourcing.
- Preparing detailed quality reports for management, highlighting key performance indicators (KPIs) and improvement initiatives.
- Maintaining accurate records of all quality control activities and documentation.
Remote Pharmaceutical Quality Control Analyst
Posted today
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Job Description
Responsibilities:
- Perform a variety of analytical tests on pharmaceutical raw materials, intermediates, and finished products.
- Operate and maintain laboratory equipment such as HPLC, GC, UV-Vis spectrophotometers, and dissolution testers.
- Analyze test results, identify deviations, and report findings to management.
- Document all laboratory activities in compliance with GLP and GMP guidelines.
- Participate in the validation and qualification of analytical methods and equipment.
- Troubleshoot analytical procedures and equipment malfunctions.
- Collaborate with cross-functional teams to investigate quality issues and implement corrective/preventative actions (CAPA).
- Ensure the proper calibration and maintenance of laboratory instrumentation.
- Maintain detailed records and ensure data integrity.
- Stay updated on relevant regulatory requirements and industry best practices.
Qualifications:
- Bachelor's or Master's degree in Chemistry, Pharmacy, Pharmaceutical Sciences, or a related field.
- Minimum of 3 years of experience in pharmaceutical quality control or analytical development.
- Proficiency in various analytical techniques (e.g., HPLC, GC, Spectroscopy, Titration).
- Strong understanding of GLP, GMP, and relevant regulatory guidelines (e.g., ICH, FDA).
- Experience with laboratory information management systems (LIMS) is a plus.
- Excellent analytical, problem-solving, and documentation skills.
- Ability to work independently and manage time effectively in a remote environment.
- Strong written and verbal communication skills.
Remote Pharmaceutical Quality Control Analyst
Posted 1 day ago
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Job Description
Responsibilities:
- Review and interpret analytical data from raw materials, in-process samples, and finished products.
- Perform data integrity checks and ensure compliance with regulatory guidelines (e.g., FDA, EMA).
- Develop, validate, and transfer analytical methods for various pharmaceutical dosage forms.
- Troubleshoot analytical instrumentation and methods to resolve issues effectively.
- Prepare detailed analytical reports, summaries, and certificates of analysis.
- Contribute to the investigation of out-of-specification (OOS) results and deviations.
- Maintain accurate and organized laboratory records and documentation.
- Stay updated on current industry trends, regulatory requirements, and scientific advancements in pharmaceutical quality control.
- Collaborate with cross-functional teams, including R&D, manufacturing, and regulatory affairs.
- Participate in internal and external audits as required.
- Ensure adherence to all safety protocols and company policies.
- Bachelor's or Master's degree in Chemistry, Pharmacy, Pharmaceutical Sciences, or a closely related field.
- Minimum of 3-5 years of experience in pharmaceutical quality control or analytical development.
- Strong knowledge of analytical techniques such as HPLC, GC, UV-Vis, IR, and dissolution testing.
- Familiarity with GLP and GMP regulations.
- Excellent data interpretation and analytical skills.
- Proficiency in using laboratory information management systems (LIMS) and other relevant software.
- Strong written and verbal communication skills.
- Ability to work independently, manage time effectively, and meet deadlines in a remote setting.
- Experience with data review and electronic record-keeping is essential.
- Knowledge of the pharmaceutical landscape in regions like Malindi, Kilifi, KE is an added advantage.
Senior Pharmaceutical Quality Control Scientist
Posted 1 day ago
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Job Description
Senior Quality Control Specialist - Industrial Cleaning Solutions
Posted today
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Job Description
Key Responsibilities:
- Develop, implement, and refine comprehensive quality control plans and procedures for industrial cleaning services.
- Establish key performance indicators (KPIs) for service quality and monitor performance against targets.
- Conduct regular remote audits and assessments of cleaning processes, methodologies, and outcomes.
- Analyze quality data, identify trends, and pinpoint areas for improvement.
- Develop and deliver training materials for cleaning teams on quality standards, safety protocols, and best practices.
- Investigate and resolve quality-related complaints or issues from clients, working collaboratively with operations teams.
- Ensure compliance with all relevant health, safety, and environmental regulations (e.g., OSHA, local environmental laws).
- Maintain detailed records of quality control activities, audit findings, and corrective actions taken.
- Collaborate with operations management to implement process improvements and enhance service efficiency.
- Stay updated on new cleaning technologies, chemicals, and equipment to ensure the highest standards of service.
- Prepare regular quality reports for senior management, highlighting key findings and recommendations.
- Champion a culture of quality and continuous improvement throughout the organization.
- Participate in client meetings to discuss service quality and address any concerns.
- Bachelor's degree in a relevant field (e.g., Chemistry, Environmental Science, Business Administration) or equivalent practical experience.
- Minimum of 5 years of experience in quality control, quality assurance, or operations management, preferably within the cleaning or facilities management industry.
- Proven track record of developing and implementing successful quality control systems.
- Strong understanding of industrial cleaning processes, chemicals, equipment, and safety procedures.
- Excellent analytical and problem-solving skills, with a keen eye for detail.
- Proficiency in data analysis and reporting.
- Exceptional written and verbal communication skills.
- Ability to work independently, manage time effectively, and maintain high productivity in a remote setting.
- Strong knowledge of health, safety, and environmental regulations related to cleaning services.
- Experience in training and development is a plus.
- Familiarity with ISO 9001 or other quality management systems is desirable.
Remote Quality Assurance Engineer - Manufacturing
Posted 1 day ago
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Job Description
Key Responsibilities:
- Develop, implement, and maintain quality assurance protocols and standards for manufacturing.
- Conduct virtual inspections and audits of manufacturing processes and finished products.
- Analyze product defects and identify root causes, proposing corrective and preventive actions.
- Collaborate with production, engineering, and R&D teams to ensure product quality throughout the lifecycle.
- Develop and manage quality control documentation, including SOPs, work instructions, and inspection plans.
- Monitor key quality metrics and KPIs, reporting on performance and trends.
- Ensure compliance with relevant industry standards and regulatory requirements.
- Train production staff on quality standards and procedures.
- Participate in the review of new product designs and manufacturing processes for quality implications.
- Manage non-conformance reporting and resolution processes.
- Drive continuous improvement initiatives to enhance product quality and reduce waste.
- Stay updated on emerging quality management techniques and technologies.
- Facilitate quality review meetings with cross-functional teams.
- Contribute to the development and implementation of quality management systems (e.g., ISO 9001).
Qualifications:
- Bachelor's degree in Engineering (Mechanical, Industrial, or relevant field), Quality Management, or a related discipline.
- Minimum of 5-7 years of experience in Quality Assurance within a manufacturing environment.
- Proven expertise in quality control methodologies and tools (e.g., Six Sigma, Lean, SPC).
- Strong understanding of manufacturing processes and best practices.
- Experience with quality management systems (e.g., ISO 9001, GMP).
- Excellent analytical, problem-solving, and critical thinking skills.
- Proficiency in data analysis and statistical tools.
- Strong written and verbal communication skills, with the ability to document technical information clearly.
- Ability to work independently, manage multiple projects, and meet deadlines in a remote setting.
- Experience with quality inspection equipment and techniques.
- Familiarity with product testing and validation processes.
- Ability to interpret technical drawings and specifications.
This remote Quality Assurance Engineer position offers a critical role in ensuring the high standards of our client's manufactured products, allowing you to apply your expertise from anywhere. If you are a dedicated QA professional with a passion for quality and a proven track record in manufacturing environments, we encourage you to apply. You will play a vital role in maintaining product integrity, customer satisfaction, and regulatory compliance. Your ability to drive quality initiatives and resolve complex issues remotely will be highly valued. We are seeking a self-motivated, detail-oriented individual who can effectively implement and oversee quality processes from a distance, contributing to the overall success and reputation of our client's manufacturing operations. Your commitment to excellence will be key in this challenging and rewarding role.
Senior Pharmaceutical Quality Assurance Specialist
Posted 4 days ago
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Job Description
Responsibilities:
- Develop, implement, and maintain robust Quality Assurance systems and procedures.
- Review and approve pharmaceutical batch records and associated documentation.
- Conduct internal audits to ensure compliance with Good Manufacturing Practices (GMP) and regulatory guidelines.
- Investigate deviations, out-of-specification (OOS) results, and customer complaints.
- Manage the change control process, assessing the impact of proposed changes on product quality.
- Ensure adherence to all applicable national and international pharmaceutical regulations.
- Collaborate with cross-functional teams (e.g., R&D, Manufacturing, Regulatory Affairs) to address quality issues.
- Participate in the qualification and validation of equipment and processes.
- Prepare and present quality-related reports and metrics.
- Contribute to the continuous improvement of quality processes and systems.
- Bachelor'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, ICH guidelines, and regulatory requirements for pharmaceuticals.
- Experience with quality management systems (QMS) and electronic documentation systems.
- Strong analytical, problem-solving, and decision-making skills.
- Excellent written and verbal communication skills.
- Ability to work independently and manage multiple tasks effectively in a remote setting.
- Meticulous attention to detail and commitment to accuracy.
- Experience with auditing and inspection readiness is highly desirable.
- Proficiency in using virtual collaboration and documentation tools.
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Senior Pharmaceutical Quality Assurance Manager
Posted 6 days ago
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Job Description
Key Responsibilities:
- Develop, implement, and maintain comprehensive Quality Management Systems (QMS).
- Ensure compliance with cGMP, ICH, FDA, and other relevant global regulatory guidelines.
- Conduct internal audits and participate in external audits of vendors and partners.
- Manage deviations, out-of-specifications (OOS), and out-of-trend (OOT) investigations and implement Corrective and Preventive Actions (CAPA).
- Review and approve batch records, validation protocols, and reports.
- Develop and manage QA documentation, including SOPs, specifications, and change controls.
- Provide training to personnel on quality systems and regulatory compliance.
- Monitor and analyze quality metrics, identifying trends and areas for continuous improvement.
- Oversee product release activities and ensure products meet all release criteria.
- Collaborate with R&D, manufacturing, and regulatory affairs departments to ensure quality throughout product development.
- Manage product complaints and recalls, if necessary.
- Lead and mentor the QA team, fostering a culture of quality excellence.
- Stay updated on changes in regulatory requirements and industry best practices.
- Participate in regulatory submissions and inspections.
- Review analytical methods and validation.
Senior Pharmaceutical Quality Assurance Specialist
Posted 6 days ago
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Job Description
Responsibilities:
- Develop, implement, and maintain robust Quality Management Systems (QMS) in accordance with cGMP, ICH guidelines, and other relevant regulatory standards.
- Oversee and conduct quality audits, both internal and external, to ensure compliance and identify areas for improvement.
- Review and approve critical quality documents, including batch records, validation protocols, SOPs, and change controls.
- Investigate deviations, out-of-specification results, and customer complaints, implementing effective corrective and preventive actions (CAPA).
- Participate in regulatory inspections and respond to queries from health authorities.
- Lead and mentor junior QA team members, fostering a culture of quality and continuous improvement.
- Ensure that all pharmaceutical products meet predefined quality attributes and regulatory requirements.
- Collaborate with R&D, manufacturing, and regulatory affairs departments to ensure seamless quality integration.
- Monitor and analyze quality metrics and trends, reporting findings to senior management.
- Manage vendor qualification and ongoing supplier quality agreements.
- Stay current with evolving pharmaceutical regulations and industry best practices.
- Contribute to the validation of manufacturing processes, analytical methods, and equipment.
- Act as a key stakeholder in product lifecycle management, ensuring quality considerations are integrated at every stage.
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field.
- Minimum of 7 years of experience in pharmaceutical quality assurance or quality control.
- In-depth knowledge of cGMP, FDA regulations, ICH guidelines, and other relevant pharmaceutical quality standards.
- Proven experience with QMS implementation, audit management, and CAPA systems.
- Strong understanding of pharmaceutical manufacturing processes and analytical testing.
- Excellent analytical, problem-solving, and critical thinking skills.
- Exceptional written and verbal communication skills, with the ability to clearly articulate complex quality-related issues.
- Detail-oriented with a high degree of accuracy.
- Ability to manage multiple projects simultaneously and meet deadlines.
- Experience in regulatory affairs is a plus.
- Proficiency in using quality management software and data analysis tools.
- Ability to work independently and collaboratively in a remote team environment.
Join our dedicated team and contribute to delivering safe and effective pharmaceutical products to patients worldwide.
Senior Pharmaceutical Quality Assurance Specialist
Posted 7 days ago
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