1,038 Senior Analytical Chemist Pharmaceutical Development jobs in Kenya
Senior Analytical Chemist - Pharmaceutical Development
Posted 14 days ago
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Job Description
Our client, a leading pharmaceutical research and development organization, is seeking a highly skilled Senior Analytical Chemist to contribute to their drug discovery and development pipeline. This is a fully remote position, allowing you to work from your preferred location while making critical contributions. You will be responsible for developing, validating, and implementing analytical methods for the characterization of active pharmaceutical ingredients (APIs) and drug products. This involves utilizing a wide range of advanced analytical techniques, including High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), Mass Spectrometry (MS), Spectroscopy (UV-Vis, FTIR, NMR), and dissolution testing. You will play a key role in method development, transfer, and troubleshooting, ensuring robustness and compliance with regulatory guidelines (e.g., ICH, FDA). A significant part of this role involves analyzing preclinical and clinical study samples, interpreting complex data, and preparing comprehensive reports. Collaboration with formulation scientists, process chemists, and quality control teams is essential to support seamless drug development. The ideal candidate will have a deep understanding of analytical chemistry principles, extensive hands-on experience with analytical instrumentation, and a proven ability to solve challenging analytical problems. Experience with data analysis software and statistical methods is also crucial. We are looking for a meticulous, detail-oriented individual with excellent scientific judgment and strong communication skills. This is an outstanding opportunity to join a cutting-edge research environment and contribute to the advancement of novel therapeutics in a flexible, remote setting.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Develop, optimize, and validate analytical methods for APIs and drug products.
- Perform qualitative and quantitative analysis using a variety of advanced analytical techniques.
- Operate and maintain analytical instrumentation (e.g., HPLC, GC, MS, Spectrophotometers).
- Analyze samples from preclinical and clinical studies.
- Interpret complex analytical data and generate comprehensive reports.
- Troubleshoot analytical methods and instrumentation issues.
- Ensure compliance with Good Laboratory Practice (GLP) and ICH guidelines.
- Collaborate with R&D, formulation, and QC teams.
- Contribute to regulatory submissions by providing analytical data and documentation.
- Stay updated on the latest advancements in analytical chemistry and pharmaceutical sciences.
Qualifications:
- Ph.D. or M.Sc. in Analytical Chemistry, Pharmaceutical Chemistry, or a related field.
- Minimum of 6 years of experience in pharmaceutical analytical development.
- Extensive hands-on experience with HPLC, GC, MS, and various spectroscopic techniques.
- Strong knowledge of method validation principles and regulatory guidelines (ICH, FDA).
- Experience with dissolution testing and other relevant pharmaceutical analysis techniques.
- Proficiency in data analysis software (e.g., ChemStation, Empower, MassHunter) and statistical tools.
- Excellent scientific problem-solving and critical thinking skills.
- Strong written and verbal communication skills.
- Ability to work independently and manage time effectively in a remote environment.
- Detail-oriented with a commitment to data integrity and accuracy.
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Remote Pharmaceutical Formulation Scientist - Drug Development
Posted 19 days ago
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Job Description
Our client, a rapidly growing pharmaceutical company dedicated to developing life-changing therapies, is seeking a highly skilled and innovative Remote Pharmaceutical Formulation Scientist. This is a fully remote position, enabling you to contribute to groundbreaking drug development from anywhere. You will be responsible for designing, developing, and optimizing novel drug delivery systems and formulations for both small molecules and biologics. Your expertise will be critical in translating preclinical research into viable, manufacturable drug products. This role involves extensive laboratory work (potentially through collaboration with external labs or supported home labs), data analysis, and scientific documentation. You will collaborate closely with chemists, pharmacologists, and manufacturing teams to advance drug candidates through the development pipeline. A strong understanding of pharmaceutics, physical chemistry, and regulatory requirements is essential.
Responsibilities:
Responsibilities:
- Design and develop stable, effective, and manufacturable pharmaceutical formulations for various routes of administration.
- Investigate and characterize drug substances and excipients to understand their impact on formulation performance.
- Conduct formulation development studies, including pre-formulation, formulation screening, optimization, and stability testing.
- Utilize various drug delivery technologies and approaches to enhance bioavailability, targeted delivery, or patient compliance.
- Perform analytical testing to characterize formulations, such as dissolution, particle size analysis, and viscosity.
- Scale-up formulation processes from laboratory bench to pilot scale.
- Prepare comprehensive technical reports, research summaries, and regulatory submission documents.
- Collaborate with analytical development, process development, and regulatory affairs teams.
- Stay current with scientific literature, emerging technologies, and regulatory guidelines in pharmaceutics and drug delivery.
- Troubleshoot formulation-related challenges and provide scientific insights.
- Ph.D. or Master's degree in Pharmaceutical Sciences, Pharmaceutics, Chemical Engineering, Chemistry, or a related discipline.
- Minimum of 5 years of experience in pharmaceutical formulation development within the industry.
- Proven track record of successful formulation development for small molecules and/or biologics.
- Hands-on experience with various dosage forms (e.g., oral solids, injectables, topical).
- Proficiency in analytical techniques relevant to formulation characterization.
- Strong understanding of physical chemistry, materials science, and biopharmaceutics.
- Familiarity with Good Manufacturing Practices (GMP) and regulatory submission requirements (e.g., FDA, EMA).
- Excellent problem-solving, critical thinking, and data analysis skills.
- Strong written and verbal communication skills, with the ability to present complex scientific information clearly.
- Demonstrated ability to work independently and manage research projects effectively in a remote setting.
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Senior Pharmaceutical Formulation Scientist - Drug Development
Posted 11 days ago
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Job Description
Our client, a progressive pharmaceutical company, is looking for a Senior Pharmaceutical Formulation Scientist to join our dynamic drug development team. This is a fully remote position, allowing you to contribute to groundbreaking pharmaceutical research from your home office. The successful candidate will be responsible for the design, development, and optimization of novel drug formulations for a wide range of therapeutic areas. You will conduct pre-formulation studies, select appropriate excipients, and develop robust manufacturing processes for both solid and liquid dosage forms. Key responsibilities include performing stability studies, characterizing formulations using various analytical techniques, and preparing documentation for regulatory submissions. You will collaborate closely with analytical development, quality control, and regulatory affairs departments to ensure successful product development. This role requires a deep understanding of pharmaceutical sciences, drug delivery systems, and regulatory guidelines. The ideal candidate holds a Master's or Ph.D. in Pharmaceutical Sciences, Chemistry, Chemical Engineering, or a related discipline, with at least 5 years of hands-on experience in pharmaceutical formulation development. Proven expertise in developing various dosage forms, including oral solid, parenteral, and topical formulations, is essential. Experience with controlled-release technologies and bioavailability enhancement is highly desirable. Strong analytical, problem-solving, and project management skills are critical. Excellent written and verbal communication abilities are necessary for effective collaboration and documentation in this remote setting. This opportunity offers the chance to significantly contribute to the pipeline of innovative medicines and advance your career in pharmaceutical research and development, working remotely with a collaborative and forward-thinking team. You will be at the forefront of creating new therapeutic solutions that can improve patient outcomes globally. The position demands a meticulous approach to scientific investigation and a commitment to delivering high-quality, effective pharmaceutical products.
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Biopharmaceutical Research Scientist
Posted 9 days ago
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Job Description
Our client is seeking a highly motivated and skilled Biopharmaceutical Research Scientist to contribute to groundbreaking research and development projects. This is a hybrid role, offering a blend of remote work flexibility and essential on-site laboratory collaboration. You will play a crucial role in designing, executing, and analyzing experiments aimed at discovering and developing novel therapeutics. Your responsibilities will include performing advanced cell-based assays, molecular biology techniques, and evaluating drug candidates. You will be expected to interpret complex experimental data, draw meaningful conclusions, and present findings to research teams and senior management. The ideal candidate will possess a strong understanding of immunology, molecular pharmacology, or a related field, with hands-on experience in relevant laboratory techniques. Proficiency in data analysis software and scientific report writing is essential. You will collaborate closely with a multidisciplinary team of scientists and researchers, contributing to project planning and strategy. The ability to troubleshoot experimental challenges and develop innovative solutions is highly valued. Strong written and verbal communication skills are necessary for effective team collaboration and presentation of results. This role requires a meticulous approach to experimental design, execution, and documentation, ensuring scientific rigor and reproducibility. Familiarity with Good Laboratory Practices (GLP) and regulatory requirements in drug development is a plus. As part of the hybrid model, you will need to effectively manage your time between remote data analysis and on-site laboratory work, demonstrating excellent organizational skills and proactivity. We are looking for a passionate scientist eager to make a significant impact in the field of biopharmaceutical innovation and contribute to the advancement of life-saving medicines. This is a stimulating environment for intellectual growth and career advancement within a forward-thinking research organization.
Job Location: Mlolongo, Machakos, KE
Job Location: Mlolongo, Machakos, KE
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Formulation & Development Manager
Posted today
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Job Description
Company Description
Dawa Life Sciences is a Life Sciences company specializing in health care, founded in 1994 by Dr. Raju Mohindra and Dr. Ajay Patel. We focus on providing affordable, high-quality pharmaceuticals and animal health products to improve communities' quality of life. Our operations are divided into Pharmaceuticals, which ensures access to treatment for various therapeutic areas in 25 African markets, and Animal Health, which markets products for livestock and companion animals. Dawa Life Sciences is committed to making a significant positive impact across the region.
Role Description
- Formulation and Product Development
: Lead the development of new formulations, processes, and packaging materials to ensure our products remain competitive and aligned with market demands. - Process Optimization:
Oversee the scale-up and optimization of manufacturing processes, ensuring efficiency and quality standards are met, while training manufacturing and quality control teams. - SOP Development:
Create, review, and implement Standard Operating Procedures (SOPs) for the F&D department to maintain consistency and compliance. - Project Management:
Plan, coordinate, and manage all activities and projects within the F&D department, ensuring timely delivery and adherence to budgets. - Analytical Method Development:
Lead the development of analytical methods for new products to ensure accuracy and reliability in testing and quality assurance. - Data Management:
Provide data and technical support for regulatory dossier preparation for both new and existing formulations.
Must-Have: Minimum Requirements
To be considered, these minimum requirements must be evident on your resume.
- Bachelor's degree in Pharmacy, Chemistry-related field, and Master's in a relevant field. Doctorate in a relevant field is an added advantage Minimum ten (10) years' experience in research and development in the pharmaceutical field three of which should be at managerial level.
- Knowledge of regulatory requirements, new product introduction and packaging technology within the pharmaceutical industry.
- Prior experience in product development and formulation in the pharmaceutical industry.
Skills and Attributes
· Innovative and good problem-solving skills
· Passion for science/formulation in pharmaceuticals
· Keep abreast with technological advancements in the pharmaceutical industry
· Management and leadership skills
· Strategic decision-making approach in response to business needs
· Good report writing skills
· Computer Literacy, i.e. Ms. Word, Excel, PowerPoint, Access etc.
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4
Lead Pharmaceutical Formulation Scientist (Pharmaceutical)
Posted 17 days ago
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Job Description
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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5
Pharmaceutical Quality Control Manager
Posted 23 days ago
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Job Description
Join our esteemed pharmaceutical company as a Pharmaceutical Quality Control Manager, based at our state-of-the-art facility in **Mlolongo, Machakos, KE**. In this pivotal role, you will be responsible for ensuring that all pharmaceutical products meet the highest standards of quality and safety. Your duties will encompass the development, implementation, and maintenance of robust quality control systems and procedures. You will lead a team of quality control analysts, overseeing all aspects of laboratory testing, from raw material analysis to finished product release. This includes validating analytical methods, ensuring compliance with Good Manufacturing Practices (GMP) and other relevant regulatory requirements (e.g., WHO, FDA guidelines). You will conduct regular audits, identify areas for improvement, and implement corrective and preventive actions (CAPA). Your expertise will be crucial in troubleshooting quality issues and driving continuous improvement initiatives across the manufacturing process. We are looking for a candidate with a strong background in pharmaceutical quality assurance and control, excellent leadership abilities, and a meticulous attention to detail. A Bachelor's or Master's degree in Pharmacy, Chemistry, or a related life science discipline is required, coupled with substantial experience in pharmaceutical quality management. A thorough understanding of regulatory frameworks and quality standards within the pharmaceutical industry is essential. You must be adept at data analysis, risk assessment, and report generation. This non-remote position requires your presence on-site to directly supervise operations and ensure operational excellence. If you are dedicated to upholding the highest quality standards and possess the leadership acumen to manage a critical function, we invite you to apply for this challenging opportunity.
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Pharmaceutical Quality Control Manager
Posted today
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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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7
Principal Scientist - Pharmaceutical Drug Discovery
Posted 15 days ago
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Job Description
Our client, a leading innovator in the pharmaceutical industry, is looking for a highly accomplished Principal Scientist to lead critical initiatives in drug discovery, operating within a fully remote, research-focused environment. This senior role demands exceptional scientific acumen, a deep understanding of molecular biology, medicinal chemistry, or a related field, and a proven track record of successfully advancing drug candidates through preclinical stages. You will be responsible for designing and executing complex research programs, mentoring a team of scientists, and collaborating with internal and external partners to achieve therapeutic breakthroughs. The ideal candidate will possess strong leadership qualities, excellent communication skills, and the ability to think strategically and creatively. Expertise in target identification and validation, assay development, high-throughput screening, and lead optimization is crucial. Experience with specific therapeutic areas or disease targets will be a significant advantage. This position offers a unique opportunity to shape the future of medicine and make a tangible difference in patient lives, all from the convenience of a remote work setup. While the operational hub may be associated with **Malindi, Kilifi, KE**, the role is entirely remote, allowing top-tier talent to contribute irrespective of geographical constraints. We expect candidates to demonstrate a high degree of scientific rigor, independence, and the ability to foster innovation within a virtual research team. Your contributions will be vital in identifying novel therapeutic targets and developing promising drug candidates for unmet medical needs. The successful applicant will be a visionary scientist capable of guiding complex projects to fruition in a collaborative, decentralized setting.
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Pharmaceutical Quality Control Analyst
Posted 8 days ago
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Job Description
Our client, a leading pharmaceutical company, is looking for a meticulous and experienced Pharmaceutical Quality Control Analyst to join their team. This role requires a blend of remote work and on-site presence, ensuring flexibility while maintaining critical laboratory operations. You will be responsible for performing a range of analytical tests on raw materials, in-process samples, and finished pharmaceutical products to ensure they meet stringent quality standards and regulatory requirements. Your duties will include operating and maintaining laboratory equipment, developing and validating analytical methods, documenting test results accurately, and investigating any deviations or out-of-specification results. The ideal candidate will possess a Bachelor's degree in Pharmacy, Chemistry, or a related scientific discipline, with proven experience in pharmaceutical quality control. Strong knowledge of GMP (Good Manufacturing Practices) and relevant analytical techniques (e.g., HPLC, GC, spectroscopy) is essential. Excellent analytical, problem-solving, and documentation skills are paramount. You must be highly organized, detail-oriented, and capable of working effectively both independently and as part of a collaborative team in a hybrid work model. This role offers a fantastic opportunity to contribute to the quality and safety of pharmaceutical products, supporting operations in the **Garissa, Garissa, KE** area.
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