What Pharmaceutical Jobs are in Kenya?

Our client, a leading pharmaceutical manufacturer, is seeking a dedicated Pharmaceutical Microbiologist to join their Quality Control department in Garissa, Kenya . This vital role involves ensuring the microbial quality and safety of pharmaceutical products by conducting a range of microbiological tests and analyses. You will be responsible for maintaining a sterile laboratory environment, validating microbiological methods, and investigating any microbial contamination issues. The ideal candidate possesses strong technical skills in microbiology, a thorough understanding of pharmaceutical quality standards, and a commitment to upholding product integrity. This is an excellent opportunity to contribute to public health by ensuring the safety of essential medicines.

• Perform routine microbiological testing on raw materials, in-process samples, and finished products.
• Conduct environmental monitoring of manufacturing areas and cleanrooms.
• Perform microbial identification and contamination investigations.
• Develop, validate, and transfer new microbiological test methods.
• Maintain accurate laboratory records and prepare test results reports.
• Ensure compliance with Good Manufacturing Practices (GMP) and other relevant regulatory guidelines.
• Calibrate and maintain laboratory equipment, ensuring proper functioning.
• Assist in the qualification of new equipment and utilities.
• Stay updated on the latest advancements in pharmaceutical microbiology and regulatory requirements.
• Participate in internal audits and support regulatory inspections as needed.

• Bachelor's degree in Microbiology, Biology, Biochemistry, or a related life science discipline.
• Minimum of 3 years of experience in pharmaceutical quality control microbiology or a related laboratory setting.
• Hands-on experience with various microbiological techniques, including aseptic sampling, microbial enumeration, and identification methods.
• Proficiency in microbial limit testing, sterility testing, and endotoxin testing.
• Familiarity with GMP requirements and regulatory guidelines for pharmaceutical manufacturing.
• Strong analytical, problem-solving, and critical thinking skills.
• Excellent attention to detail and meticulous record-keeping abilities.
• Good communication and interpersonal skills.
• Ability to work independently and as part of a team in a laboratory environment.
• Experience working in Garissa, Kenya or a similar regional setting is a plus.

Our client offers a competitive salary and a comprehensive benefits package, including health insurance, paid time off, and retirement savings plans. Employees benefit from opportunities for professional development through internal training programs and workshops. We foster a collaborative and safe work environment where your contributions are valued. This role provides the opportunity to work with a dedicated team focused on ensuring the highest standards of pharmaceutical quality and safety. Join a company committed to making a difference in healthcare.

• Develop and implement effective sales strategies to achieve and exceed sales targets for the assigned territory.
• Build and maintain strong, long-lasting relationships with healthcare professionals and key opinion leaders.
• Present and articulate the features and benefits of pharmaceutical products clearly and persuasively.
• Organize and conduct product presentations, and educational meetings for healthcare providers.
• Monitor competitor activities and market trends to adapt sales strategies accordingly.
• Maintain accurate records of sales activities, customer interactions, and expenses using the company's CRM system.
• Collaborate with the marketing team to provide feedback on market needs and product performance.
• Ensure compliance with all company policies, ethical standards, and regulatory requirements.
• Achieve territory sales quotas and call objectives.
• Attend regional and national sales meetings and training sessions.

• Bachelor's degree in Pharmacy, Pharmacology, Biology, or a related science field. A business or marketing degree with relevant experience will also be considered.
• Minimum of 3 years of experience in pharmaceutical sales, preferably within the **pharmaceutical** sector.
• Proven track record of meeting or exceeding sales targets.
• Excellent understanding of the Kenyan healthcare system and the pharmaceutical market, especially in the coastal region.
• Strong negotiation, communication, and interpersonal skills.
• Ability to travel extensively within the assigned territory and manage time effectively.
• Familiarity with CRM software and reporting tools.
• Valid driver's license and a clean driving record.
• Reside in or be willing to relocate to the Mombasa, Mombasa, KE area.
• Professional appearance and demeanor.

• Develop and execute regulatory strategies for product registration and lifecycle management in various markets.
• Prepare, review, and submit regulatory dossiers to health authorities (e.g., NMPA, FDA, EMA).
• Ensure compliance with all relevant national and international pharmaceutical regulations and guidelines.
• Act as the primary point of contact with regulatory agencies and health authorities.
• Monitor changes in the regulatory environment and assess their impact on the company's products and operations.
• Provide regulatory guidance and support to R&D, manufacturing, and commercial teams.
• Oversee the review of labeling, promotional materials, and advertising for regulatory compliance.
• Manage regulatory inspections and audits.
• Contribute to the development and implementation of regulatory policies and procedures.
• Lead and mentor a team of regulatory affairs professionals.

• Master's degree or Ph.D. in Pharmacy, Chemistry, Biology, or a related scientific discipline.
• Minimum of 7 years of progressive experience in regulatory affairs within the **pharmaceutical** industry.
• Proven track record of successfully managing product registrations and regulatory submissions in diverse markets.
• In-depth knowledge of global regulatory requirements, including ICH guidelines.
• Strong understanding of drug development, manufacturing, and quality assurance processes.
• Excellent leadership, project management, and communication skills.
• Ability to think strategically and provide practical solutions to complex regulatory challenges.
• Proficiency in regulatory information management systems.
• Experience working in a remote or hybrid environment is advantageous.
• Must be based in Kenya, with the capacity to work remotely from **Eldoret, Uasin Gishu, KE** or any other suitable location.

• Assist CRAs and investigators with the preparation, maintenance, and filing of essential trial documents (e.g., Investigator Site Files - ISF).
• Manage and track study supplies and investigational medicinal products at trial sites.
• Assist in the preparation and distribution of study-related materials.
• Schedule and coordinate investigator meetings, site initiation visits, and monitoring visits.
• Assist with data entry and management, ensuring accuracy and completeness of trial data.
• Communicate with investigative sites to gather required information or documentation.
• Ensure compliance with Good Clinical Practice (GCP) and company SOPs.
• Prepare site visit reports and follow-up on action items.
• Support the setup and maintenance of Electronic Data Capture (EDC) systems.
• Perform administrative tasks as needed to support the clinical operations team.

• High school diploma or equivalent; a Bachelor's degree in a life science, healthcare, or related field is a plus.
• Previous experience in an administrative role, preferably within a clinical research or **pharmaceutical** setting.
• Familiarity with clinical trial processes and terminology is advantageous.
• Strong organizational skills and meticulous attention to detail.
• Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook).
• Excellent communication and interpersonal skills.
• Ability to multitask and prioritize workload effectively in a fast-paced environment.
• Proactive attitude and willingness to learn.
• Knowledge of GCP principles is a plus.
• Must be based in or willing to relocate to **Malindi, Kilifi, KE**.

Our client, a distinguished pharmaceutical company dedicated to patient safety, is actively seeking a meticulous and knowledgeable Pharmaceutical Pharmacovigilance Specialist to join their team in Garissa . This crucial role involves the monitoring, detection, assessment, and prevention of adverse effects and other medicine-related problems. You will be responsible for managing adverse event reports, ensuring regulatory compliance, and contributing to the overall safety profile of our client's pharmaceutical products. The ideal candidate possesses a strong understanding of pharmacovigilance principles, regulatory requirements, and a keen eye for detail. This hybrid position offers a dynamic work environment, balancing essential on-site responsibilities with potential remote strategic contributions and reporting.

• Collect, process, and assess adverse event reports from various sources (e.g., healthcare professionals, patients, literature).
• Ensure timely and accurate reporting of adverse events to regulatory authorities in accordance with global requirements.
• Maintain the pharmacovigilance database, ensuring data integrity and completeness.
• Perform case narrative writing and safety data analysis.
• Contribute to the preparation of Periodic Safety Update Reports (PSURs) and other safety documents.
• Monitor safety literature for relevant publications and emerging safety signals.
• Collaborate with internal departments (e.g., Clinical, Regulatory, Medical Information) to ensure comprehensive safety surveillance.
• Assist in the development and review of pharmacovigilance SOPs and guidelines.
• Participate in regulatory inspections and internal audits related to pharmacovigilance activities.
• Stay up-to-date with evolving global pharmacovigilance regulations and guidelines.

• Bachelor's degree in Pharmacy, Nursing, Medicine, Life Sciences, or a related healthcare field.
• Minimum of 3 years of experience in pharmacovigilance or drug safety.
• Solid understanding of pharmacovigilance principles, methodologies, and regulatory requirements (e.g., FDA, EMA guidelines).
• Experience with adverse event reporting systems and databases.
• Proficiency in analyzing and interpreting safety data.
• Excellent written and verbal communication skills, with the ability to write clear and concise case narratives.
• Strong organizational skills and meticulous attention to detail.
• Ability to manage multiple tasks and meet strict deadlines.
• Proficiency in Microsoft Office Suite.
• Experience with medical coding (MedDRA) is highly desirable.

Our client offers a competitive salary, comprehensive health, dental, and vision insurance, and a strong retirement savings plan. Employees are provided with opportunities for professional development, continuous learning, and career advancement within the organization. The company fosters a collaborative and patient-centric culture, valuing the contributions of each team member.

Our client, a forward-thinking pharmaceutical company, is seeking an experienced Senior Pharmaceutical Development Scientist to join their innovative team in Kakamega, Kenya . This hybrid role involves leading the development of new pharmaceutical products, from early-stage formulation design through to process optimization for clinical and commercial manufacturing. You will play a key role in translating drug candidates into viable dosage forms, ensuring product stability, efficacy, and manufacturability. The ideal candidate possesses a strong scientific background in pharmaceutical sciences, extensive experience in formulation and process development, and excellent leadership skills. This is a significant opportunity to drive product innovation and contribute to the company's growth.

• Lead the formulation development of solid dosage forms (tablets, capsules) and potentially other dosage forms.
• Design and execute pre-formulation studies, including solid-state characterization and solubility enhancement.
• Develop robust and scalable manufacturing processes for new drug products.
• Conduct stability studies and interpret results to define shelf-life and storage conditions.
• Oversee technology transfer activities to manufacturing sites and external partners.
• Troubleshoot formulation and process-related challenges during development and scale-up.
• Collaborate with analytical development, regulatory affairs, and manufacturing teams.
• Prepare development reports, protocols, and sections of regulatory submissions.
• Mentor junior scientists and provide technical guidance to the development team.
• Stay abreast of new technologies and scientific advancements in pharmaceutical development.

• Ph.D. or Master's degree in Pharmaceutical Sciences, Pharmaceutics, Chemical Engineering, or a related field.
• Minimum of 6 years of progressive experience in pharmaceutical product development.
• Proven expertise in formulation design, process development, and scale-up of oral solid dosage forms.
• Strong understanding of drug delivery principles, excipient science, and material characterization techniques.
• Experience with GMP manufacturing environments and regulatory requirements is essential.
• Excellent analytical, problem-solving, and project management skills.
• Strong leadership capabilities and the ability to mentor team members.
• Effective written and verbal communication skills, with the ability to present complex scientific information clearly.
• Ability to work effectively in a hybrid environment in Kakamega, Kenya .
• Experience with advanced manufacturing technologies is a plus.

Our client offers a highly competitive salary and benefits package, including performance-based bonuses, comprehensive health insurance, and retirement savings plans. Employees are provided with ample opportunities for professional growth, including training, attendance at scientific conferences, and career advancement pathways. We cultivate a collaborative and innovative work environment that supports work-life balance. Additional benefits include generous paid vacation, potential for relocation assistance, and access to state-of-the-art research facilities. Join a company dedicated to developing innovative therapies that improve patient lives.