85 Pharmaceutical Manager jobs in Kenya
Remote Pharmaceutical Product Manager
Posted today
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Key responsibilities include conducting market research, analyzing competitive landscapes, and identifying unmet medical needs. You will collaborate closely with R&D, clinical affairs, regulatory affairs, marketing, and sales teams to ensure successful product development and market penetration. This role requires a deep understanding of the pharmaceutical industry, regulatory pathways, and market dynamics. You will also be responsible for developing product positioning, messaging, and go-to-market strategies.
The ideal candidate will possess strong leadership, strategic thinking, and project management skills. Excellent communication and presentation abilities are crucial for effectively conveying product strategies to diverse stakeholders, including senior management and external partners. Experience in managing pharmaceutical products, preferably in a remote setting, is highly desirable. You should be adept at analyzing market data, forecasting sales, and making data-driven decisions to optimize product performance. This role offers the challenge of shaping the future of healthcare through impactful product management in a flexible, remote environment.
Qualifications:
- Bachelor's degree in Pharmacy, Life Sciences, Business, or a related field. Master's degree (MBA or relevant scientific degree) is highly preferred.
- Minimum of 5 years of experience in product management within the pharmaceutical industry.
- Proven experience in market analysis, product strategy development, and commercialization.
- Deep understanding of the pharmaceutical drug development process and regulatory affairs.
- Strong project management skills and ability to manage cross-functional teams.
- Excellent analytical, communication, and presentation skills.
- Experience with market access and reimbursement strategies is a plus.
- Ability to work independently and effectively in a remote team environment.
Pharmaceutical Quality Assurance Manager
Posted today
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Pharmaceutical Quality Assurance Manager
Posted today
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Job Description
Key Responsibilities:
- Develop and maintain the company's Quality Management System (QMS).
- Ensure compliance with GMP, GDP, and other relevant pharmaceutical regulations.
- Oversee quality control processes and testing procedures.
- Conduct internal audits and manage corrective and preventive actions (CAPAs).
- Manage deviation, investigation, and change control processes.
- Review and approve batch records and validation documentation.
- Lead and mentor the Quality Assurance team.
- Collaborate with cross-functional departments to maintain product quality.
Pharmaceutical Quality Assurance Manager
Posted today
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Pharmaceutical Quality Assurance Manager
Posted 2 days ago
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Key responsibilities include ensuring all pharmaceutical products meet stringent quality specifications and regulatory standards. You will lead investigations into quality deviations, implement corrective and preventive actions (CAPAs), and manage change control processes. The ideal candidate will possess extensive knowledge of pharmaceutical regulations, quality assurance methodologies, and risk management principles. Strong leadership, analytical, and problem-solving skills are essential. Excellent communication and interpersonal skills are required to collaborate effectively with various departments and regulatory bodies. Our client offers a supportive and compliant remote work environment, valuing the expertise and dedication of its Quality Assurance team. This role demands a rigorous, systematic, and compliance-driven professional committed to ensuring the safety and efficacy of pharmaceutical products.
Responsibilities:
- Develop, implement, and maintain the company's Quality Management System (QMS).
- Ensure compliance with pharmaceutical regulations, including GMP, GCP, and GDP.
- Oversee quality control testing and product release processes.
- Conduct internal audits and support external regulatory inspections.
- Lead investigations into quality deviations and implement CAPAs.
- Manage change control processes to ensure product integrity.
- Review and approve batch records, validation protocols, and quality-related documents.
- Monitor key quality metrics and provide regular reports to management.
- Train and mentor QA staff and other personnel on quality procedures.
- Master's or Ph.D. in Pharmacy, Chemistry, Biology, or a related scientific field.
- Minimum of 8 years of experience in Quality Assurance within the pharmaceutical industry.
- In-depth knowledge of cGMP, GCP, GDP, and other relevant regulatory guidelines.
- Proven experience in managing QMS, conducting audits, and leading investigations.
- Strong understanding of pharmaceutical manufacturing processes and product development.
- Excellent analytical, problem-solving, and decision-making skills.
- Exceptional written and verbal communication skills.
- Ability to manage complex quality systems and processes remotely.
- Strong leadership and team management capabilities.
Pharmaceutical Quality Assurance Manager
Posted 2 days ago
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Pharmaceutical Quality Assurance Manager
Posted 3 days ago
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Job Description
Responsibilities:
- Develop, implement, and maintain the company's Quality Management System (QMS) in compliance with GMP, ICH, and other relevant pharmaceutical regulations.
- Oversee all quality assurance activities, including batch record review, deviation investigations, CAPA management, change control, and internal audits.
- Ensure that all pharmaceutical products manufactured or distributed meet established specifications and regulatory standards.
- Review and approve validation protocols and reports for manufacturing processes, analytical methods, and equipment.
- Manage and mentor the QA team, providing guidance and support to ensure high performance and professional development.
- Act as the primary point of contact for regulatory agency inspections and audits, facilitating and coordinating responses.
- Monitor and assess the performance of suppliers and contract manufacturers, ensuring their compliance with quality agreements.
- Drive continuous improvement initiatives to enhance product quality, process efficiency, and regulatory compliance.
- Stay updated on current pharmaceutical regulations, industry trends, and best practices in quality assurance.
- Prepare and present quality metrics and reports to senior management.
Qualifications:
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
- Minimum of 7 years of experience in Quality Assurance within the pharmaceutical industry, with at least 3 years in a managerial or supervisory role.
- In-depth knowledge of Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and regulatory guidelines (e.g., FDA, EMA, ICH).
- Experience with pharmaceutical product development, manufacturing, and quality control.
- Proven ability to manage audits, inspections, and investigations.
- Excellent analytical, problem-solving, and decision-making skills.
- Strong leadership, communication, and interpersonal skills, with the ability to effectively manage a remote team.
- Proficiency in quality management software and tools.
- Detail-oriented with a strong commitment to quality and compliance.
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Pharmaceutical Quality Assurance Manager
Posted 4 days ago
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Pharmaceutical Quality Assurance Manager
Posted 5 days ago
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Key responsibilities include:
- Developing, implementing, and maintaining the company's Quality Management System (QMS) in accordance with regulatory guidelines (e.g., FDA, EMA, PIC/S).
- Leading and supervising the QA team, including quality control personnel.
- Conducting regular internal audits to ensure compliance with GMP and other relevant regulations.
- Managing and participating in external audits and inspections by regulatory authorities.
- Reviewing and approving batch records, validation protocols, and other quality-related documentation.
- Investigating deviations, out-of-specification (OOS) results, and customer complaints, and implementing corrective and preventive actions (CAPAs).
- Overseeing change control processes and ensuring that all changes are properly evaluated and documented.
- Developing and delivering training programs on GMP and quality assurance principles for all relevant personnel.
- Monitoring key quality indicators (KQIs) and providing reports to senior management on the overall quality performance.
- Ensuring that all materials and products released meet the required quality specifications.
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) in accordance with cGMP (current Good Manufacturing Practices) and other relevant regulatory guidelines.
- Oversee all Quality Assurance operations, including batch record review, deviation management, change control, and CAPA (Corrective and Preventive Actions).
- Ensure that all pharmaceutical products manufactured meet specified quality standards and regulatory requirements.
- Conduct internal audits and participate in external audits by regulatory agencies and customers.
- Manage and mentor the QA team, providing guidance and fostering professional development.
- Review and approve validation protocols and reports for manufacturing processes, equipment, and analytical methods.
- Develop and maintain Standard Operating Procedures (SOPs) and other quality-related documentation.
- Investigate product quality complaints and implement appropriate corrective actions.
- Monitor and analyze quality data to identify trends and opportunities for improvement.
- Ensure compliance with relevant national and international pharmaceutical regulations.
- Liaise with regulatory authorities on quality-related matters.
- Manage the supplier qualification program to ensure the quality of incoming materials.
- Lead quality risk assessments and implement mitigation strategies.
- Prepare for and participate in regulatory inspections and customer audits.
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific field. A Ph.D. is a plus.
- Minimum of 8 years of progressive experience in Quality Assurance within the pharmaceutical industry, with at least 3 years in a managerial or supervisory role.
- In-depth knowledge of cGMP, ICH guidelines, and other relevant pharmaceutical regulations (e.g., FDA, EMA).
- Proven experience in developing and implementing robust Quality Management Systems.
- Strong understanding of pharmaceutical manufacturing processes, analytical testing, and quality control procedures.
- Excellent leadership, team management, and communication skills.
- Strong analytical and problem-solving abilities.
- Proficiency in risk management principles and tools.
- Experience with regulatory inspections and audits.
- Ability to manage multiple projects and priorities in a fast-paced environment.
- Excellent documentation and report-writing skills.
- Familiarity with electronic quality management systems (eQMS) is desirable.