2,004 Pharmaceutical Science jobs in Kenya
Biopharmaceutical Research Scientist
Posted 7 days ago
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Job Location: Mlolongo, Machakos, KE
Lead Pharmaceutical Formulation Scientist (Pharmaceutical)
Posted 15 days ago
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Lead Pharmaceutical Research Scientist (Biotechnology)
Posted 20 days ago
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Principal Pharmaceutical Scientist - Drug Discovery and Development
Posted 19 days ago
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Responsibilities:
- Lead and direct research projects focused on identifying and validating novel drug targets and developing innovative small molecule or biologic drug candidates.
- Design, synthesize, and characterize novel chemical entities with therapeutic potential.
- Conduct rigorous preclinical studies, including in vitro and in vivo pharmacology, toxicology, and pharmacokinetic assessments.
- Develop and optimize drug delivery systems and formulation strategies.
- Collaborate effectively with a globally distributed, remote team of chemists, biologists, pharmacologists, and clinicians.
- Analyze and interpret complex experimental data, providing strategic direction for drug discovery programs.
- Author scientific publications, patents, and regulatory documents.
- Mentor and guide junior scientists, fostering a collaborative and innovative research environment.
- Stay at the forefront of scientific advancements in relevant therapeutic areas and drug discovery technologies.
- Contribute to the strategic planning and portfolio management of drug development projects, considering various markets including Embu, Embu, KE , for future commercialization.
- Manage external collaborations with academic institutions and contract research organizations (CROs).
- Ph.D. in Medicinal Chemistry, Pharmacology, Pharmaceutical Sciences, or a closely related field.
- Minimum of 10 years of relevant industry experience in drug discovery and preclinical development.
- Demonstrated expertise in a specific therapeutic area (e.g., oncology, infectious diseases, CNS disorders).
- Strong understanding of drug metabolism and pharmacokinetics (DMPK), toxicology, and regulatory requirements for drug development.
- Proven track record of successfully leading drug discovery projects and advancing candidates into clinical trials.
- Excellent scientific judgment, critical thinking, and problem-solving skills.
- Exceptional written and verbal communication skills, essential for remote collaboration and scientific dissemination.
- Experience with scientific literature databases (e.g., SciFinder, PubMed) and data analysis software.
- Ability to work independently and manage multiple research projects concurrently in a remote setting.
- A strong publication record in peer-reviewed journals and relevant patent filings is highly advantageous.
Principal Scientist - Pharmaceutical Drug Discovery
Posted 13 days ago
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Lead Pharmaceutical Quality Control Scientist
Posted 9 days ago
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Principal Pharmaceutical Quality Control Scientist
Posted 22 days ago
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Key Responsibilities:
- Develop, validate, and implement analytical methods for raw materials, in-process samples, and finished pharmaceutical products using techniques such as HPLC, GC, UV-Vis, FTIR, and dissolution testing.
- Oversee and conduct stability studies according to ICH guidelines to assess product shelf-life and storage conditions.
- Review and approve batch records, analytical data, and quality control reports to ensure product quality and regulatory compliance.
- Investigate deviations, out-of-specification (OOS) results, and out-of-trend (OOT) data, determining root causes and implementing corrective and preventive actions (CAPAs).
- Contribute to the design and execution of validation protocols for analytical methods and equipment.
- Ensure that all quality control activities comply with cGMP, FDA, and other relevant regulatory agency requirements.
- Train and mentor junior QC scientists and technicians, providing technical guidance and support.
- Collaborate with R&D, manufacturing, and regulatory affairs departments to resolve quality issues and support product lifecycle management.
- Maintain laboratory equipment, ensuring proper calibration, maintenance, and documentation.
- Stay abreast of new scientific advancements, regulatory changes, and industry best practices in pharmaceutical quality control.
Qualifications:
- Master's or Ph.D. in Pharmaceutical Sciences, Chemistry, Analytical Chemistry, or a related field.
- A minimum of 10 years of experience in pharmaceutical quality control, with at least 3 years in a lead or principal scientist role.
- Extensive hands-on experience with a variety of analytical techniques relevant to pharmaceutical quality control.
- Strong knowledge of cGMP regulations, ICH guidelines, and pharmacopeial standards (USP, EP).
- Proven experience in method validation, OOS investigations, and CAPA management.
- Excellent analytical, problem-solving, and critical thinking skills.
- Strong leadership, communication, and interpersonal skills, with the ability to effectively manage remote teams and projects.
- Proficiency in laboratory information management systems (LIMS) and other relevant software.
- Detail-oriented with a commitment to accuracy and quality.
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Senior Pharmaceutical Quality Control Scientist
Posted 13 days ago
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Key responsibilities include:
- Developing, validating, and implementing analytical methods for raw materials, intermediates, and finished pharmaceutical products using techniques such as HPLC, GC, UV-Vis, and dissolution testing.
- Performing routine quality control testing according to established protocols and regulatory guidelines (e.g., GMP, ICH).
- Investigating and troubleshooting Out-of-Specification (OOS) results and deviations, providing detailed root cause analysis.
- Maintaining laboratory equipment, ensuring proper calibration, and adhering to all safety procedures.
- Reviewing and approving analytical data, batch records, and method validation reports.
- Participating in regulatory inspections and audits, ensuring compliance with all relevant standards.
- Collaborating with R&D, manufacturing, and regulatory affairs departments to resolve quality-related issues.
- Staying current with the latest advancements in pharmaceutical analysis and quality control.
- Contributing to the continuous improvement of quality systems and processes.
- Training and mentoring junior QC analysts on analytical techniques and procedures.
The ideal candidate will possess a Master's or Ph.D. in Pharmaceutical Sciences, Chemistry, Analytical Chemistry, or a related field, with a minimum of 5 years of experience in pharmaceutical quality control. Extensive hands-on experience with analytical instrumentation (HPLC, GC, spectroscopy) and method validation is essential. A thorough understanding of Good Manufacturing Practices (GMP), ICH guidelines, and other relevant regulatory requirements is mandatory. Excellent analytical, problem-solving, and documentation skills are critical. Strong communication and interpersonal skills are necessary for effective remote collaboration with cross-functional teams. You will be remotely contributing to ensuring the highest standards of quality for our pharmaceutical products, supporting operations that may involve **Machakos, Machakos, KE**. This is an exceptional opportunity to make a significant impact in ensuring drug safety and efficacy. We are looking for a detail-oriented scientist with a passion for quality and a commitment to excellence in pharmaceutical manufacturing.
Remote Pharmaceutical Quality Control Scientist
Posted 12 days ago
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Remote Pharmaceutical Formulation Scientist - Drug Development
Posted 17 days ago
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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.