Quality Control Supervisor

80201 Nairobi, Nairobi KES110000 Annually WhatJobs

Posted 2 days ago

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full-time
Our client, a rapidly expanding manufacturing firm specializing in consumer goods, is seeking a meticulous and proactive Quality Control Supervisor to lead its remote quality assurance operations. This pivotal role will involve developing, implementing, and monitoring quality control systems across all production stages, ensuring adherence to stringent international standards and client specifications. You will be responsible for identifying areas for improvement, driving defect reduction initiatives, and fostering a culture of quality excellence within the organization. This position requires a keen analytical mind, a deep understanding of quality management methodologies, and the ability to manage teams effectively in a virtual setting. Responsibilities include:
  • 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.
The successful candidate will possess a Bachelor's degree in Engineering, Quality Management, or a related technical field. A minimum of 5 years of experience in quality control or quality assurance within a manufacturing environment is required, with supervisory experience being essential. Strong knowledge of ISO 9001 or other relevant quality management systems is mandatory. Proficiency in statistical process control (SPC) and data analysis tools is highly desirable. Excellent leadership, problem-solving, and communication skills are crucial for success in this remote role. This is an excellent opportunity to shape the quality framework of a growing company from a remote location, influencing product integrity and customer satisfaction. The operational oversight will be for production facilities near **Malindi, Kilifi, KE**, though the role is fully remote.
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Remote Pharmaceutical Quality Control Analyst

80202 Nairobi, Nairobi KES120000 Annually WhatJobs

Posted today

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full-time
Our client is seeking a dedicated and meticulous Pharmaceutical Quality Control Analyst to join their fully remote team. In this crucial role, you will be instrumental in ensuring the quality and integrity of pharmaceutical products through rigorous testing and analysis. Your primary responsibilities will include performing various laboratory tests on raw materials, in-process samples, and finished products using a range of analytical techniques and instrumentation. You will meticulously document all test results, prepare detailed reports, and identify any deviations from established specifications. A key part of your role will involve troubleshooting analytical methods and instrumentation to ensure accuracy and reliability. You will also participate in the validation of new analytical methods and equipment. Collaboration with other departments, such as Research & Development and Manufacturing, will be essential to address quality issues and implement corrective actions. This position demands a deep understanding of Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and relevant regulatory guidelines (e.g., FDA, EMA). You will be responsible for maintaining laboratory equipment, ensuring its calibration and functionality. A strong grasp of data integrity principles is paramount. This is an excellent opportunity for a skilled analyst to contribute to the development and production of safe and effective medicines from the comfort of their home office. We are looking for candidates who are highly organized, detail-oriented, and possess excellent problem-solving skills. The ability to work independently and manage time effectively in a remote setting is critical. You will be expected to maintain a professional and efficient remote workspace. Our client is committed to fostering a culture of quality and continuous improvement, and this role is central to achieving those goals. Successful applicants will demonstrate a passion for pharmaceutical science and a commitment to upholding the highest standards of quality. Opportunities for professional growth and development within a forward-thinking pharmaceutical organization are available.

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.
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Remote Pharmaceutical Quality Control Analyst

80101 Nairobi, Nairobi KES100000 Annually WhatJobs

Posted 1 day ago

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full-time
Our client, a reputable pharmaceutical company, is seeking a meticulous and experienced Remote Pharmaceutical Quality Control Analyst. This role is crucial for ensuring the quality, safety, and efficacy of pharmaceutical products through rigorous testing and analysis. As a fully remote position, you will primarily conduct laboratory data review, develop and validate analytical methods, and contribute to quality assurance processes from your home office. The ideal candidate possesses a strong background in analytical chemistry or a related pharmaceutical science, exceptional attention to detail, and a thorough understanding of Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). You will play a vital role in maintaining regulatory compliance and upholding the highest standards of product quality.

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.
Qualifications:
  • 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.
This fully remote position offers a significant opportunity for a dedicated QC professional to contribute to the pharmaceutical industry's integrity and innovation. You will work on critical aspects of product quality assurance, ensuring that patients receive safe and effective medications. The flexibility of remote work allows for a better work-life balance while performing essential scientific duties.
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Senior Pharmaceutical Quality Control Scientist

80200 Nairobi, Nairobi KES7000000 Annually WhatJobs

Posted 1 day ago

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full-time
Our client is seeking a highly skilled and dedicated Senior Pharmaceutical Quality Control Scientist to ensure the highest standards of product quality and regulatory compliance. This is a fully remote position, allowing you to contribute to vital research and development from anywhere. The ideal candidate will possess a strong background in analytical chemistry, pharmaceutical sciences, and Good Manufacturing Practices (GMP). You will be responsible for developing, validating, and implementing analytical methods for raw materials, in-process samples, and finished products. This role involves conducting complex testing, troubleshooting analytical issues, and interpreting data to ensure product integrity. Key responsibilities include operating and maintaining advanced analytical instrumentation (e.g., HPLC, GC, Mass Spectrometry), managing laboratory operations, and preparing detailed technical reports. You will also play a crucial role in deviation investigations, change control management, and ensuring compliance with regulatory guidelines from bodies such as the FDA and EMA. The successful candidate must have excellent analytical, problem-solving, and documentation skills. A thorough understanding of quality systems and regulatory requirements in the pharmaceutical industry is essential. Experience with statistical analysis and data integrity principles is highly desirable. This remote position offers a unique opportunity to contribute to the development and manufacturing of life-saving medicines. We are looking for a meticulous, detail-oriented professional with a passion for quality and a commitment to scientific excellence. A Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or a related discipline, along with at least 5 years of relevant experience in pharmaceutical quality control, is required. Join our client and be instrumental in upholding the quality and safety of pharmaceutical products on a global scale, all while enjoying the convenience and flexibility of remote work.
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Senior Quality Control Specialist - Industrial Cleaning Solutions

80100 Nairobi, Nairobi KES85000 Annually WhatJobs

Posted today

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full-time
Our client, a leading provider of specialized industrial cleaning services, is seeking an experienced Senior Quality Control Specialist to enhance their operational excellence from a fully remote capacity. This critical role will be responsible for developing, implementing, and monitoring stringent quality assurance protocols across all service delivery platforms. You will be instrumental in ensuring that our cleaning solutions meet and exceed industry standards, client expectations, and regulatory requirements. This is a fantastic opportunity to contribute to a vital sector, driving standards and best practices through a remote-first approach.

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.
Qualifications:
  • 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.
This remote role is essential for maintaining our reputation for excellence in industrial cleaning services.
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Remote Quality Assurance Engineer - Manufacturing

80100 Nairobi, Nairobi KES140000 Annually WhatJobs

Posted 1 day ago

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full-time
Our client is seeking a meticulous and experienced Remote Quality Assurance Engineer specializing in manufacturing processes. This is a fully remote role, where you will be instrumental in ensuring the quality and consistency of manufactured goods by developing and implementing robust quality control systems and procedures from your home office. You will work closely with production teams to identify potential defects, troubleshoot issues, and drive continuous improvement in product quality. The ideal candidate possesses a deep understanding of manufacturing quality standards, analytical skills, and a commitment to upholding excellence.

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.
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Senior Pharmaceutical Quality Assurance Specialist

80100 Nairobi, Nairobi KES100000 Annually WhatJobs

Posted 4 days ago

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Job Description

full-time
Our client, a distinguished pharmaceutical company at the forefront of medical innovation, is seeking a meticulous and experienced Senior Pharmaceutical Quality Assurance Specialist to join their fully remote quality team. This role is paramount in ensuring that our client's pharmaceutical products meet the highest standards of quality, safety, and efficacy. The ideal candidate will possess a strong understanding of regulatory requirements (e.g., GMP, FDA, EMA), a keen eye for detail, and extensive experience in quality assurance within the pharmaceutical industry. As a remote specialist, you will leverage digital tools to review documentation, conduct internal audits virtually, and contribute to the continuous improvement of quality systems. Your responsibilities will include developing and implementing quality control procedures, reviewing batch records, investigating deviations and out-of-specification results, managing change control processes, and ensuring compliance with all relevant pharmaceutical regulations. This is an exceptional opportunity for a dedicated quality professional seeking a challenging and rewarding remote role where their contributions directly impact patient safety and product integrity. The ability to meticulously analyze data, write clear and concise reports, and collaborate effectively with global teams is essential. If you are a detail-oriented individual with a passion for upholding the highest quality standards in pharmaceuticals and desire a flexible remote work arrangement, we encourage you to apply. Join us in our commitment to delivering life-saving medicines through unwavering quality assurance.

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.
Qualifications:
  • 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

80202 Nairobi, Nairobi KES420000 Annually WhatJobs

Posted 6 days ago

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Job Description

full-time
Our client, a respected pharmaceutical company committed to high standards of healthcare, is seeking an experienced Senior Pharmaceutical Quality Assurance Manager for a fully remote role. This position is critical in ensuring that all pharmaceutical products meet stringent quality and regulatory requirements throughout their lifecycle, from development to manufacturing and distribution. You will be responsible for establishing and maintaining robust quality management systems, conducting internal audits, managing deviations and CAPAs, and ensuring compliance with Good Manufacturing Practices (GMP) and other relevant international standards. The ideal candidate will have extensive experience in the pharmaceutical industry with a deep understanding of QA/QC principles.

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.
A minimum of 8 years of experience in Quality Assurance within the pharmaceutical or biotechnology industry is required, with at least 4 years in a management or lead role. A strong understanding of cGMP, pharmaceutical manufacturing processes, and regulatory affairs is essential. Experience with quality risk management, validation (process, cleaning, analytical), and electronic QMS is highly desirable. A Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field is required. Excellent leadership, communication, problem-solving, and analytical skills are necessary. This is a significant opportunity to uphold and advance pharmaceutical quality standards in a flexible, remote setting, supporting our client's operations relevant to Malindi, Kilifi, KE .
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Senior Pharmaceutical Quality Assurance Specialist

80200 Nairobi, Nairobi KES200000 Annually WhatJobs

Posted 6 days ago

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Job Description

full-time
Our client, a leading pharmaceutical organization, is seeking a highly experienced Senior Pharmaceutical Quality Assurance Specialist to join their esteemed, fully remote team. This role is crucial for ensuring the highest standards of quality and compliance throughout the pharmaceutical lifecycle, from development to market. We are committed to a remote-first work environment, offering flexibility and a collaborative platform for professionals dedicated to excellence in pharmaceutical quality.

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.
Qualifications:
  • 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.
This position is based in Malindi, Kilifi, KE , but operates on a fully remote basis, providing flexibility and the ability to work from any location.

Join our dedicated team and contribute to delivering safe and effective pharmaceutical products to patients worldwide.
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Senior Pharmaceutical Quality Assurance Specialist

80200 Nairobi, Nairobi KES260000 Annually WhatJobs

Posted 7 days ago

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Job Description

full-time
Our client is seeking a meticulous and experienced Senior Pharmaceutical Quality Assurance Specialist to oversee and enhance quality management systems within a remote operational framework. This critical role involves ensuring adherence to stringent regulatory standards (e.g., GMP, FDA) and industry best practices throughout the pharmaceutical product lifecycle. You will be responsible for developing, implementing, and maintaining quality assurance procedures, conducting internal audits, reviewing batch records, and managing deviations and CAPAs (Corrective and Preventive Actions). Your expertise will also extend to participating in external audits, assessing vendor quality systems, and contributing to risk management initiatives. Collaboration with R&D, manufacturing, regulatory affairs, and other key departments is essential to ensure product quality and compliance. The ideal candidate will hold a Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field, with a minimum of 7 years of experience in pharmaceutical quality assurance. A thorough understanding of GxP regulations, quality control principles, and documentation practices is paramount. Excellent analytical, problem-solving, and critical thinking skills are required, along with strong written and verbal communication abilities. Experience with electronic quality management systems (eQMS) and a proven ability to manage complex QA projects in a remote setting are highly desirable. This is a significant opportunity to contribute to the integrity and safety of pharmaceutical products while enjoying the flexibility of remote work.
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