What Jobs are available for Small Scale Manufacturing in Kenya?
Showing 5000+ Small Scale Manufacturing jobs in Kenya
Pharmaceutical Quality Control Specialist
Posted 2 days ago
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Job Description
Our client is seeking a highly meticulous and diligent Pharmaceutical Quality Control Specialist to uphold the highest standards of product integrity within their operations, operating in a fully remote capacity. This role is vital in ensuring that all pharmaceutical products meet rigorous quality specifications and regulatory requirements. The ideal candidate will possess a strong understanding of pharmaceutical manufacturing processes, quality assurance principles, and relevant regulatory guidelines (e.g., GMP, ICH). You will be responsible for reviewing and analyzing batch records, conducting laboratory data analysis, and performing validation testing. This position requires exceptional attention to detail, strong analytical skills, and the ability to interpret scientific data accurately in a remote environment. Key responsibilities include identifying deviations from quality standards, participating in investigations of quality issues, and contributing to the continuous improvement of quality systems. You will collaborate with R&D, manufacturing, and regulatory affairs teams to ensure product quality throughout its lifecycle. We are looking for a candidate with a Bachelor's degree in a relevant scientific field (e.g., Pharmacy, Chemistry, Biotechnology) and a proven track record in pharmaceutical quality control. If you are a proactive professional committed to ensuring patient safety and product efficacy, and seeking a rewarding remote career, we encourage you to apply. Your home office will serve as your operational base, requiring a stable internet connection for accessing quality management systems and collaborating with colleagues. This role offers a competitive salary and the opportunity to contribute to the development and manufacturing of essential medicines. Your dedication to quality assurance will be paramount in safeguarding public health and maintaining our client's reputation for excellence.
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Remote Pharmaceutical Quality Control Specialist
Posted 2 days ago
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Our client is seeking a meticulous and experienced Remote Pharmaceutical Quality Control Specialist to ensure the highest standards of product quality and regulatory compliance. This is a fully remote position, offering a unique opportunity to contribute to the pharmaceutical industry from anywhere. You will be responsible for developing, implementing, and executing quality control procedures throughout the manufacturing and production lifecycle. This includes conducting rigorous testing of raw materials, in-process samples, and finished products to verify they meet all specified quality attributes and regulatory requirements. The ideal candidate will possess a strong understanding of Good Manufacturing Practices (GMP) and relevant pharmaceutical quality standards. Experience with analytical instrumentation and laboratory techniques used in pharmaceutical testing is essential. You will be tasked with reviewing batch records, investigating deviations and out-of-specification results, and implementing corrective and preventive actions (CAPA). Furthermore, you will contribute to the development and validation of new analytical methods and maintain comprehensive documentation of all quality control activities. Excellent attention to detail, strong problem-solving skills, and the ability to work independently with minimal supervision in a remote environment are crucial. You should be proficient in using quality management software and possess excellent written and verbal communication skills for clear reporting and collaboration. A Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific discipline is required, along with demonstrable experience in pharmaceutical quality control. This role is pivotal in safeguarding product integrity and patient safety. This position is based in **Garissa, Garissa, KE**, but operates entirely remotely.
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Senior Pharmaceutical Quality Control Specialist
Posted 2 days ago
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Job Description
Our client is seeking a highly qualified Senior Pharmaceutical Quality Control Specialist to ensure the highest standards of pharmaceutical product quality. This is a fully remote position, allowing you to contribute your expertise from any location. You will be responsible for designing and implementing robust quality control protocols, analyzing raw materials and finished products, and ensuring compliance with regulatory requirements. Your duties will include performing analytical testing, validating testing methods, documenting quality control procedures, and investigating deviations from quality standards. The ideal candidate will have a strong background in pharmaceutical sciences, with extensive experience in quality assurance and quality control within the pharmaceutical industry. Proficiency in analytical techniques such as HPLC, GC, and spectroscopy is essential. You should possess exceptional attention to detail, strong problem-solving skills, and a thorough understanding of Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP). Experience with regulatory submissions and audits is highly desirable. This role offers an exciting opportunity to make a significant impact on patient safety and product efficacy, all within a flexible remote work arrangement. You will be a key player in upholding our client's commitment to quality and regulatory excellence. We are looking for a dedicated professional who can maintain meticulous records and drive continuous improvement in quality processes. This is an ideal role for a seasoned specialist looking for a senior-level remote opportunity, contributing to the pharmaceutical sector from the heart of Kakamega, Kakamega, KE .
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Lead Pharmaceutical Formulation Scientist (Pharmaceutical)
Posted 2 days ago
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Our client is actively recruiting a highly accomplished Lead Pharmaceutical Formulation Scientist for a fully remote, full-time position. This role is central to the innovation and development of novel pharmaceutical products, from concept through to clinical trials and commercialization. The ideal candidate will possess an advanced degree (M.Sc. or Ph.D.) in Pharmaceutical Sciences, Chemistry, or a related field, coupled with extensive experience in drug formulation, pre-formulation studies, and dosage form design. You will lead the formulation development of new chemical entities (NCEs) and the improvement of existing drug products, ensuring optimal bioavailability, stability, and patient compliance. Key responsibilities include designing and executing experimental plans for solid dosage forms, sterile injectables, or other relevant dosage types, as well as troubleshooting formulation challenges. You will interpret complex analytical data, conduct characterization studies, and ensure all activities comply with regulatory guidelines (e.g., GMP, ICH). This role involves close collaboration with analytical development, regulatory affairs, and manufacturing teams. The successful applicant will have a strong understanding of physical chemistry, material science, and their application in pharmaceutical development. Excellent project management, leadership, and communication skills are essential, enabling effective collaboration in a remote setting. If you are passionate about advancing drug development and have a proven ability to drive formulation projects from bench to clinic, we invite you to apply. This remote position allows you to contribute your expertise to our client's mission, supporting their drug discovery and development efforts potentially impacting areas around Machakos, Machakos, KE .
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Pharmaceutical Quality Control Manager
Posted 2 days ago
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Job Description
Our client is seeking a highly experienced and meticulous Pharmaceutical Quality Control Manager to oversee all aspects of quality assurance and control within their state-of-the-art facility located in Ruiru, Kiambu, KE . This critical role involves ensuring that all pharmaceutical products meet stringent regulatory standards and internal quality benchmarks before release to the market. You will be responsible for developing, implementing, and maintaining robust quality management systems, including SOPs, validation protocols, and deviation management processes. Key responsibilities include leading and mentoring the QC team, managing laboratory operations, and ensuring the accurate and timely execution of analytical testing for raw materials, in-process samples, and finished products. The ideal candidate will possess a deep understanding of Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and relevant pharmaceutical regulations (e.g., FDA, EMA). You will conduct regular audits, manage change control processes, and investigate out-of-specification (OOS) results to identify root causes and implement corrective and preventive actions (CAPA). Strong leadership, analytical thinking, and excellent communication skills are essential for this position. You will collaborate closely with Production, R&D, and Regulatory Affairs departments to ensure product quality and compliance throughout the entire lifecycle. Experience with various analytical techniques such as HPLC, GC, spectroscopy, and dissolution testing is required. The ability to drive continuous improvement initiatives within the QC department and foster a culture of quality excellence is paramount. Your contribution will be vital in safeguarding public health by ensuring the highest standards of pharmaceutical quality and safety.
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Lead Pharmaceutical Quality Control Scientist
Posted 2 days ago
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Our client, a prominent pharmaceutical firm, is searching for a seasoned Lead Pharmaceutical Quality Control Scientist to spearhead their remote quality assurance operations. This role demands a meticulous and experienced professional dedicated to upholding the highest standards of pharmaceutical quality and compliance. You will be responsible for overseeing all aspects of quality control testing, method validation, and stability studies for a diverse range of pharmaceutical products. This includes developing and implementing robust quality control procedures, ensuring adherence to Good Manufacturing Practices (GMP) and other regulatory requirements. The Lead Scientist will manage a team of quality control analysts, providing technical guidance, training, and performance management. Your expertise will be crucial in troubleshooting analytical issues, investigating deviations, and implementing corrective and preventive actions (CAPA). You will also be involved in the review and approval of batch records, analytical reports, and quality agreements. A significant part of this role involves collaborating with R&D, manufacturing, and regulatory affairs departments to ensure seamless product development and lifecycle management. This is a remote position, offering the flexibility to work from anywhere while making a critical contribution to public health. The successful candidate will possess a deep understanding of analytical techniques, instrumentation (e.g., HPLC, GC, MS), and pharmacopeial standards. Experience in pharmaceutical formulation and process development is highly desirable. You should demonstrate excellent leadership, communication, and problem-solving skills. Your commitment to quality and patient safety will be paramount. We are looking for individuals who are passionate about advancing pharmaceutical science and who can thrive in a virtual, collaborative environment. The ability to interpret complex data and translate it into actionable insights is essential.Naivasha, Nakuru, KE is the designated regional hub, but the role is fully remote.
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Pharmaceutical Quality Control Manager
Posted 5 days ago
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Job Description
Our client, a reputable pharmaceutical manufacturer, is actively seeking a highly experienced and detail-oriented Pharmaceutical Quality Control Manager to oversee their quality assurance and control operations at their facility in Thika, Kiambu, KE . This critical role ensures that all manufactured pharmaceutical products meet the highest standards of quality, safety, and efficacy, in strict adherence to national and international regulatory guidelines (e.g., GMP, ISO). You will be responsible for developing, implementing, and maintaining robust quality management systems throughout the entire production process, from raw material inspection to finished product release.
Key responsibilities include managing and leading the Quality Control laboratory team, including chemists and technicians. You will oversee routine testing of raw materials, in-process samples, and finished products using various analytical techniques. This involves setting testing specifications, validating analytical methods, and ensuring the proper calibration and maintenance of laboratory equipment. You will also investigate deviations, out-of-specification (OOS) results, and customer complaints, implementing corrective and preventive actions (CAPAs) as necessary. Collaboration with Production, Regulatory Affairs, and R&D departments is essential to ensure seamless integration of quality protocols.
The ideal candidate will hold a Bachelor's or Master's degree in Pharmacy, Chemistry, Biotechnology, or a closely related scientific field. A minimum of 8 years of progressive experience in Quality Control or Quality Assurance within the pharmaceutical industry is required, with at least 4 years in a managerial or supervisory capacity. Strong knowledge of GMP regulations, analytical testing methodologies (HPLC, GC, spectroscopy, etc.), and quality management systems is essential. Excellent leadership, problem-solving, decision-making, and communication skills are necessary. Experience with regulatory inspections and audits is highly desirable. This role requires a proactive approach to quality management and a commitment to maintaining the integrity and compliance of pharmaceutical products.
Key responsibilities include managing and leading the Quality Control laboratory team, including chemists and technicians. You will oversee routine testing of raw materials, in-process samples, and finished products using various analytical techniques. This involves setting testing specifications, validating analytical methods, and ensuring the proper calibration and maintenance of laboratory equipment. You will also investigate deviations, out-of-specification (OOS) results, and customer complaints, implementing corrective and preventive actions (CAPAs) as necessary. Collaboration with Production, Regulatory Affairs, and R&D departments is essential to ensure seamless integration of quality protocols.
The ideal candidate will hold a Bachelor's or Master's degree in Pharmacy, Chemistry, Biotechnology, or a closely related scientific field. A minimum of 8 years of progressive experience in Quality Control or Quality Assurance within the pharmaceutical industry is required, with at least 4 years in a managerial or supervisory capacity. Strong knowledge of GMP regulations, analytical testing methodologies (HPLC, GC, spectroscopy, etc.), and quality management systems is essential. Excellent leadership, problem-solving, decision-making, and communication skills are necessary. Experience with regulatory inspections and audits is highly desirable. This role requires a proactive approach to quality management and a commitment to maintaining the integrity and compliance of pharmaceutical products.
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Remote Production Supervisor - Quality Control
Posted 2 days ago
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Job Description
Our client is seeking a meticulous and experienced Remote Production Supervisor specializing in Quality Control to oversee manufacturing operations from a virtual setting. In this fully remote role, you will be responsible for establishing and maintaining stringent quality standards throughout the production process. Your primary duties will include developing and implementing comprehensive quality control protocols, conducting remote audits of manufacturing processes, and analyzing production data to identify trends and areas for improvement. You will work closely with on-site production teams, providing virtual guidance on quality procedures, defect prevention, and corrective actions. This role requires a deep understanding of manufacturing principles, statistical process control (SPC), and various quality management systems (e.g., ISO 9001). You will leverage advanced data analysis tools and software to monitor product quality, identify root causes of defects, and implement effective solutions. The ideal candidate will possess excellent analytical and problem-solving skills, with a keen eye for detail and a commitment to upholding the highest quality standards. Strong communication and leadership abilities are essential to effectively guide and motivate remote and on-site teams. A Bachelor's degree in Engineering, Manufacturing, or a related field is preferred, along with significant experience in quality control within a manufacturing environment. You must be adept at using virtual collaboration tools and communicating effectively across distances. This is an exciting opportunity for a quality control expert to contribute to operational excellence in a remote-first capacity. You will be instrumental in driving continuous improvement initiatives, reducing waste, and ensuring customer satisfaction through superior product quality. Your ability to interpret technical specifications, conduct root cause analysis, and implement robust quality assurance programs will be critical. You will also be responsible for training on-site personnel on quality standards and procedures. The successful candidate will be a self-starter, highly organized, and capable of managing complex projects independently. Familiarity with Six Sigma methodologies is a strong asset. You will play a key role in ensuring that all products meet or exceed regulatory and customer expectations, contributing significantly to the company's reputation for quality and reliability. Experience in the specific industry of the client (e.g., electronics, automotive, consumer goods) will be highly valued.
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