What Jobs are available for Quality Assurance Manager in Kenya?
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Pharmaceutical Quality Assurance Manager
Posted 1 day ago
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Key Responsibilities:
- Develop, implement, and maintain the company's Quality Management System (QMS).
- Oversee all quality assurance activities, including internal and external audits.
- Ensure compliance with Good Manufacturing Practices (GMP) and other relevant regulatory standards.
- Manage the investigation of deviations, out-of-specification (OOS) results, and customer complaints.
- Develop and implement corrective and preventive actions (CAPAs).
- Review and approve batch records, validation protocols, and other quality-related documents.
- Lead and mentor the QA team, fostering a culture of quality and compliance.
- Interface with regulatory agencies during inspections and audits.
- Conduct risk assessments and implement risk mitigation strategies.
- Drive continuous improvement initiatives within the quality assurance function.
This role requires exceptional leadership, analytical, and problem-solving skills. The ideal candidate will possess a Bachelor's or Master's degree in Pharmacy, Chemistry, or a related scientific field, with extensive experience in pharmaceutical quality assurance. Proficiency in quality management software and a thorough understanding of regulatory documentation are crucial. As a fully remote position, strong self-discipline, excellent communication skills, and the ability to manage projects autonomously are essential. You will be expected to collaborate effectively with cross-functional teams across different time zones. Our client is dedicated to producing high-quality pharmaceuticals and seeks a proactive leader to uphold their commitment to excellence.
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Principal Pharmaceutical Quality Assurance Manager
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Lead Pharmaceutical Quality Assurance Manager
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Senior Pharmaceutical Quality Assurance Manager
Posted 1 day ago
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Responsibilities:
- Develop, implement, and maintain the company's Quality Management System (QMS) in compliance with cGMP, ICH, and other relevant global regulatory standards.
- Oversee all QA activities, including batch record review and release, deviation investigations, CAPA management, change control, and internal/external audits.
- Lead and mentor a team of QA professionals, fostering a culture of quality and continuous improvement.
- Ensure all pharmaceutical manufacturing processes, documentation, and training meet rigorous quality standards.
- Manage regulatory inspections and audits, acting as the primary point of contact for health authorities.
- Review and approve validation protocols and reports for manufacturing processes, equipment, and analytical methods.
- Develop and manage quality agreements with contract manufacturers and suppliers.
- Monitor key quality metrics and KPIs, reporting on quality performance to senior management.
- Stay current with evolving pharmaceutical regulations and industry best practices.
- Participate in product development teams, providing QA input from early stages through to commercialization.
- Conduct risk assessments and implement mitigation strategies to ensure product quality and patient safety.
- Master's degree or Ph.D. in Pharmacy, Chemistry, Biology, or a related life science discipline.
- Minimum of 10 years of progressive experience in Quality Assurance within the pharmaceutical industry, with at least 5 years in a management role.
- In-depth knowledge of cGMP regulations, pharmaceutical manufacturing processes, and quality control principles.
- Proven experience in managing regulatory inspections (e.g., FDA, EMA, local authorities) and successful audit outcomes.
- Strong experience with QMS elements: CAPA, change control, deviation management, batch release, and validation.
- Excellent leadership, team management, analytical, and problem-solving skills.
- Exceptional communication, negotiation, and interpersonal skills.
- Ability to work independently, manage multiple priorities, and drive results in a remote setting.
- Proficiency in pharmaceutical quality documentation and regulatory submission processes.
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Remote Pharmaceutical Quality Assurance Manager
Posted 1 day ago
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Pharmaceutical Quality Assurance Manager - Remote
Posted 1 day ago
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Location: Thika, Kiambu, KE (Remote)
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Quality Assurance Manager - Manufacturing Standards
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Senior Pharmaceutical Quality Assurance Manager
Posted 5 days ago
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Job Description
Responsibilities:
- Develop, implement, and maintain the company's Quality Management System (QMS).
- Ensure compliance with all relevant pharmaceutical regulations (GMP, FDA, EMA, etc.).
- Lead and conduct internal and external quality audits.
- Investigate quality deviations, out-of-specification (OOS) results, and customer complaints.
- Develop and manage Corrective and Preventive Actions (CAPA) plans.
- Oversee quality control processes for raw materials, in-process, and finished products.
- Review and approve batch records, validation protocols, and reports.
- Manage product lifecycle quality, from development to post-market.
- Lead and mentor the quality assurance team.
- Promote a culture of quality and continuous improvement throughout the organization.
- Liaise with regulatory agencies during inspections and inquiries.
- Master's or Ph.D. in Pharmacy, Chemistry, Biology, or a related scientific field.
- Minimum of 10 years of experience in pharmaceutical quality assurance and quality control.
- Extensive knowledge of GMP, ICH guidelines, and global regulatory requirements.
- Proven experience in developing and managing QMS.
- Strong understanding of pharmaceutical manufacturing processes.
- Excellent leadership, communication, and interpersonal skills.
- Ability to conduct thorough investigations and implement effective CAPA.
- Experience with risk management principles and tools.
- Proficiency in quality management software is a plus.
- Demonstrated ability to work autonomously and lead teams in a remote environment.
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Lead Quality Assurance Manager - Manufacturing
Posted 1 day ago
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