85 Pharmaceutical Manager jobs in Kenya

Remote Pharmaceutical Product Manager

30200 Moiben KES400000 Annually WhatJobs

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full-time
Our client is seeking a highly analytical and strategic Remote Pharmaceutical Product Manager to lead the development and commercialization of innovative pharmaceutical products. This is a fully remote position, offering a unique opportunity to drive product strategy and market success from anywhere. You will be responsible for defining product vision, developing roadmaps, and guiding products through their entire lifecycle, from concept to market launch and beyond.

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.
This is a pivotal role for an experienced professional looking to make a significant contribution to the pharmaceutical sector.
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Pharmaceutical Quality Assurance Manager

01000 Mumbuni KES480000 Annually WhatJobs

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full-time
Our client, a prominent pharmaceutical company, is actively recruiting for a dedicated and experienced Pharmaceutical Quality Assurance Manager to join their fully remote team. This pivotal role will oversee and manage all aspects of the quality assurance program, ensuring compliance with global regulatory standards, including cGMP, ICH guidelines, and other relevant industry regulations. You will be responsible for developing, implementing, and maintaining quality systems, procedures, and documentation to support drug development, manufacturing, and post-market surveillance. Key duties include conducting internal audits, managing external audits from regulatory bodies and customers, overseeing deviation and CAPA systems, and ensuring the quality of raw materials, intermediates, and finished products. The ideal candidate will possess a deep understanding of pharmaceutical quality management systems, risk assessment methodologies, and validation principles. Strong leadership, communication, and interpersonal skills are essential, as you will guide and mentor a team of QA professionals. You will collaborate closely with various departments, including R&D, manufacturing, regulatory affairs, and supply chain, to foster a culture of quality across the organization. A bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science field is required, along with extensive experience in pharmaceutical quality assurance. This is a significant opportunity to make a substantial impact on patient safety and product quality within a respected and innovative pharmaceutical organization, offering the full benefits of remote work.
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Pharmaceutical Quality Assurance Manager

00100 Abothuguchi West KES170000 Annually WhatJobs

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full-time
Our client, a leading pharmaceutical company, is looking for a meticulous and experienced Pharmaceutical Quality Assurance Manager to join their team in Nairobi, Nairobi, KE . This hybrid role is critical in ensuring that all pharmaceutical products meet stringent quality standards and regulatory requirements throughout their lifecycle. The successful candidate will be responsible for developing, implementing, and maintaining the company's Quality Management System (QMS), which includes GMP (Good Manufacturing Practices) and GDP (Good Distribution Practices). Key responsibilities involve overseeing quality control processes, conducting internal audits, managing deviations and change controls, and ensuring proper documentation and record-keeping. You will lead and mentor a team of QA professionals, fostering a culture of quality and continuous improvement. The ideal candidate will have a Bachelor's or Master's degree in Pharmacy, Chemistry, Biotechnology, or a related life science field, with a minimum of 7 years of experience in pharmaceutical quality assurance or quality control, including significant experience in a management or supervisory role. A deep understanding of pharmaceutical regulations (e.g., FDA, EMA, WHO guidelines) is essential. Excellent analytical, problem-solving, and decision-making skills are required, along with strong leadership and communication abilities. You will collaborate closely with R&D, manufacturing, and regulatory affairs departments to ensure product quality and compliance. This position involves a blend of on-site responsibilities for audits and team oversight, with flexibility for remote work on specific tasks.

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.
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Pharmaceutical Quality Assurance Manager

10300 Bungoma, Western KES180000 Annually WhatJobs

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Job Description

full-time
Our client is actively recruiting a seasoned Pharmaceutical Quality Assurance Manager to ensure adherence to the highest industry standards. This role is office-based, requiring your presence at our state-of-the-art facility. You will be responsible for developing, implementing, and maintaining the company's Quality Management System (QMS) in compliance with regulatory requirements such as cGMP, ICH guidelines, and other relevant standards. Your duties will include conducting internal audits, reviewing batch records, managing deviations and CAPAs, and overseeing validation processes for equipment and manufacturing processes. The ideal candidate will have a strong background in pharmaceutical quality assurance or quality control, with a comprehensive understanding of regulatory affairs and compliance within the pharmaceutical industry. Excellent analytical skills, meticulous attention to detail, and proficiency in quality management software are essential. You will lead and mentor a team of QA professionals, fostering a culture of continuous improvement and quality excellence. Strong leadership, communication, and problem-solving skills are critical for effective collaboration with manufacturing, R&D, and regulatory departments. The ability to interpret complex regulations and translate them into practical operational procedures is paramount. We are seeking a proactive individual who is dedicated to upholding product integrity and patient safety. This is a key leadership position within our organization, offering significant responsibility and opportunities for professional growth in a vital sector.
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Pharmaceutical Quality Assurance Manager

80200 Nairobi, Nairobi KES9000000 Annually WhatJobs

Posted 2 days ago

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Job Description

full-time
Our client, a leading pharmaceutical company, is seeking a highly experienced and meticulous Pharmaceutical Quality Assurance Manager to ensure the highest standards of quality and compliance across their operations. This is a crucial fully remote position, enabling you to uphold critical quality protocols and manage QA systems from anywhere. You will be responsible for developing, implementing, and maintaining the company's Quality Management System (QMS) in accordance with regulatory requirements, including GMP, GCP, and GDP. Your role will involve overseeing quality control processes, conducting internal audits, and managing external audits and inspections.

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.
Qualifications:
  • 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.
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Pharmaceutical Quality Assurance Manager

60200 Meru , Eastern KES7500000 Annually WhatJobs

Posted 2 days ago

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full-time
Our client, a leading pharmaceutical company, is seeking a highly qualified and experienced Pharmaceutical Quality Assurance Manager to oversee and implement robust quality systems. This role offers a hybrid work arrangement, combining remote flexibility with essential on-site presence for critical operations. You will be responsible for ensuring that all pharmaceutical products manufactured and distributed by the company meet stringent quality standards and comply with national and international regulatory requirements (e.g., GMP, ISO). Your key responsibilities will include developing, implementing, and maintaining the Quality Management System (QMS), conducting internal audits, managing external audits, and ensuring all quality-related documentation is accurate and up-to-date. You will lead investigations into quality deviations, implement corrective and preventive actions (CAPA), and oversee product release processes. The ideal candidate will possess a strong scientific background in pharmacy, chemistry, or a related life science field, with significant experience in pharmaceutical quality assurance and regulatory affairs. Proven expertise in GMP principles and a thorough understanding of the pharmaceutical drug development and manufacturing lifecycle are essential. You must have excellent analytical, problem-solving, and decision-making skills, with a keen eye for detail. Strong leadership and people management capabilities are required to guide the QA team effectively. Excellent communication and interpersonal skills are necessary for collaborating with various departments and regulatory bodies. This role requires an individual who can balance strategic quality oversight with hands-on operational involvement, ensuring the highest standards of product quality and patient safety in a dynamic pharmaceutical environment. This is an exceptional opportunity to make a significant contribution to the quality and compliance of life-saving medications within a respected organization.
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Pharmaceutical Quality Assurance Manager

80100 Moiben KES300000 Annually WhatJobs

Posted 3 days ago

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Job Description

full-time
Our client, a growing pharmaceutical company dedicated to advancing healthcare, is seeking a highly motivated and experienced Pharmaceutical Quality Assurance Manager for a fully remote role. This position is crucial for maintaining the highest standards of quality across our product lines, ensuring compliance with regulatory requirements, and fostering a culture of continuous improvement. The ideal candidate will leverage their deep understanding of pharmaceutical manufacturing processes and quality systems to oversee all QA activities. You will play a key role in ensuring product safety, efficacy, and consistency from development through to market release. This role offers the unique benefit of being entirely remote, allowing you to contribute to our mission from the comfort of your home office while collaborating with a global team.

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.
This role demands a proactive individual with a strategic approach to quality management. If you are passionate about ensuring pharmaceutical quality and thrive in a remote work environment, we encourage you to apply.
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Pharmaceutical Quality Assurance Manager

20117 Naivasha, Rift Valley KES160000 Annually WhatJobs

Posted 4 days ago

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full-time
Our client is looking for a highly experienced and detail-oriented Pharmaceutical Quality Assurance Manager to oversee quality control processes at their facility in **Naivasha, Nakuru, KE**. This critical role ensures that all products meet stringent regulatory standards and internal quality specifications. You will be responsible for developing, implementing, and maintaining comprehensive quality management systems. Key responsibilities include creating and reviewing Standard Operating Procedures (SOPs), conducting internal audits, managing documentation, and ensuring compliance with Good Manufacturing Practices (GMP) and other relevant pharmaceutical regulations. You will also lead investigations into deviations and out-of-specification results, implement corrective and preventive actions (CAPA), and manage the batch release process. The ideal candidate possesses a strong background in pharmaceutical quality assurance, with in-depth knowledge of regulatory requirements from agencies like the FDA and EMA. Excellent leadership, communication, and problem-solving skills are essential. You should have a proven ability to manage teams, drive quality initiatives, and foster a culture of quality throughout the organization. Experience with risk management and validation processes is highly desirable. We seek a dedicated professional committed to upholding the highest standards of quality and safety in pharmaceutical manufacturing. Your expertise will be crucial in maintaining product integrity and ensuring patient safety.
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Pharmaceutical Quality Assurance Manager

50201 Bungoma, Western KES150000 Annually WhatJobs

Posted 5 days ago

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full-time
Our client is seeking a highly experienced and meticulous Pharmaceutical Quality Assurance Manager to oversee quality systems and compliance in **Bungoma, Bungoma, KE**. This critical role ensures that all pharmaceutical products manufactured by our client meet rigorous quality standards and regulatory requirements. The ideal candidate will have a strong background in pharmaceutical manufacturing, GMP (Good Manufacturing Practices), and quality control. You will be responsible for developing, implementing, and maintaining the Quality Management System (QMS), conducting internal audits, and managing external regulatory inspections.

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.
A Master's degree in Pharmacy, Chemistry, Biology, or a related scientific field is required, along with a minimum of 7 years of experience in the pharmaceutical industry, with at least 3 years in a management or supervisory role within Quality Assurance or Quality Control. In-depth knowledge of GMP, ICH guidelines, and regulatory requirements is essential. Strong leadership, analytical, problem-solving, and communication skills are required. This hybrid role allows for collaboration with the on-site team while maintaining flexibility.
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Pharmaceutical Quality Assurance Manager

30100 Moiben KES220000 month WhatJobs

Posted 5 days ago

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full-time
Our client, a leading pharmaceutical company committed to producing high-quality medicines, is seeking a seasoned Pharmaceutical Quality Assurance Manager for their facility in **Eldoret, Uasin Gishu, KE**. The successful candidate will be responsible for establishing, implementing, and maintaining the company's Quality Management System (QMS) to ensure compliance with regulatory standards and industry best practices. This role involves overseeing quality control processes and providing leadership in all QA-related activities, with a hybrid approach to work balancing on-site responsibilities and remote strategic planning.

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.
Qualifications:
  • 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.
This is a pivotal role for our client's operations in **Eldoret, Uasin Gishu, KE**, ensuring the integrity and safety of their pharmaceutical products. Join a company dedicated to health and innovation.
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