5,885 Remote Pharmaceutical Quality Control Analyst jobs in Kenya
Senior Pharmaceutical Quality Control Analyst (No Remote)
Posted 21 days ago
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Job Description
Responsibilities:
- Perform analytical testing on raw materials, intermediates, and finished pharmaceutical products using various techniques (e.g., HPLC, GC, UV-Vis, Karl Fischer titration).
- Develop, validate, and transfer analytical methods according to regulatory requirements.
- Operate, calibrate, and maintain laboratory equipment to ensure accuracy and reliability.
- Interpret analytical data, identify out-of-specification (OOS) results, and conduct investigations.
- Document all laboratory activities, results, and deviations in compliance with GMP and GxP guidelines.
- Prepare Certificates of Analysis (CoA) and technical reports.
- Collaborate with cross-functional teams, including R&D, Manufacturing, and Regulatory Affairs.
- Participate in internal and external audits.
- Contribute to process improvements and the implementation of new technologies in the QC lab.
- Ensure a safe working environment and adherence to all safety protocols.
- Mentor and train junior QC analysts.
- Stay current with relevant pharmacopoeias and regulatory updates.
- Bachelor's degree or Master's degree in Chemistry, Pharmaceutical Sciences, or a related discipline.
- Minimum of 5 years of hands-on experience in pharmaceutical quality control or analytical development.
- Extensive experience with analytical instrumentation such as HPLC, GC, and spectrophotometers.
- Thorough understanding of GMP, ICH guidelines, and pharmacopoeial standards (e.g., USP, EP).
- Proficiency in method development, validation, and troubleshooting.
- Strong data interpretation and analytical skills.
- Excellent documentation and report-writing abilities.
- Meticulous attention to detail and commitment to accuracy.
- Good laboratory practices (GLP) knowledge is a plus.
- Effective communication and teamwork skills.
Senior Pharmaceutical Quality Control Analyst - Remote
Posted 22 days ago
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Job Description
Key Responsibilities:
- Perform a wide range of analytical tests on raw materials, in-process samples, and finished pharmaceutical products using various laboratory techniques (e.g., HPLC, GC, spectroscopy).
- Develop, validate, and implement new analytical methods according to regulatory guidelines (e.g., FDA, EMA, WHO).
- Analyze test results, interpret data, and prepare detailed reports, ensuring accuracy and completeness.
- Ensure all laboratory activities comply with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).
- Maintain laboratory equipment, calibrate instruments, and troubleshoot any technical issues.
- Investigate out-of-specification (OOS) results and deviations, identifying root causes and implementing corrective and preventive actions (CAPAs).
- Collaborate with cross-functional teams, including R&D, manufacturing, and regulatory affairs.
- Contribute to the development and improvement of quality control procedures and protocols.
- Maintain accurate and up-to-date laboratory records and documentation.
- Participate in internal and external audits as required.
- Stay current with advancements in pharmaceutical analysis and regulatory requirements.
- Provide training and guidance to junior analysts as needed.
- Master's degree or PhD in Pharmacy, Chemistry, Analytical Chemistry, or a related life science field.
- Minimum of 7 years of experience in pharmaceutical quality control analysis.
- Extensive hands-on experience with analytical instrumentation (HPLC, GC, UV-Vis, IR, etc.).
- In-depth knowledge of pharmaceutical GMP, GLP, and relevant regulatory guidelines.
- Proven experience in method development and validation.
- Strong understanding of pharmacopeial standards (e.g., USP, EP).
- Excellent analytical, problem-solving, and critical-thinking skills.
- Proficiency in data analysis and statistical software.
- Strong written and verbal communication skills, essential for reporting and collaboration.
- Ability to work independently and manage time effectively in a remote setting.
- Meticulous attention to detail and a commitment to quality and accuracy.
Remote Quality Control Specialist - Sanitation
Posted 22 days ago
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Job Description
Your primary responsibility will be to develop, implement, and monitor quality control protocols for cleaning and sanitation services. This involves establishing clear operational standards, conducting virtual audits and assessments of cleaning procedures, and analyzing performance data to identify areas for improvement. You will be instrumental in ensuring compliance with health and safety regulations and company-specific hygiene policies. This role requires an in-depth understanding of best practices in cleaning, disinfection, and waste management.
The ideal candidate will possess excellent analytical skills, a keen eye for detail, and strong communication abilities. You will collaborate with on-site cleaning supervisors and management teams, providing remote guidance, training support, and feedback to maintain consistently high levels of cleanliness and hygiene. Proficiency in using digital tools for reporting, data analysis, and virtual assessments is essential. This position offers a unique opportunity to shape and uphold critical sanitation standards within the organization, contributing to a safe and healthy environment for all, while enjoying the flexibility of remote work.
Key Responsibilities:
- Develop, implement, and refine quality control standards for cleaning and sanitation services.
- Conduct virtual audits and assessments of cleaning operations and procedures.
- Analyze performance data and identify trends to drive continuous improvement.
- Ensure adherence to health and safety regulations and industry best practices.
- Provide remote guidance and support to on-site cleaning teams and supervisors.
- Develop training materials and resources for cleaning staff.
- Investigate and resolve quality-related issues and customer complaints.
- Prepare regular reports on quality performance, compliance, and areas for enhancement.
- Stay updated on the latest advancements in cleaning technologies and sanitation protocols.
- Maintain accurate records and documentation of quality control activities.
Qualifications:
- High school diploma or equivalent; Bachelor's degree in Environmental Health, Public Health, Hospitality Management, or a related field is a plus.
- Minimum of 4 years of experience in quality control, sanitation management, or a related field within the cleaning or hospitality industry.
- Demonstrated knowledge of cleaning chemicals, equipment, and best practices in sanitation and hygiene.
- Experience in developing and implementing quality assurance programs.
- Proficiency in using digital tools for data analysis, reporting, and virtual communication.
- Strong analytical and problem-solving skills.
- Excellent written and verbal communication skills.
- Ability to work independently and manage time effectively in a remote setting.
- Attention to detail and a commitment to maintaining high standards.
- Understanding of relevant health and safety regulations (e.g., OSHA, WHO guidelines).
Remote Quality Control Specialist - Cleaning Services
Posted 21 days ago
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Job Description
Key Responsibilities:
- Develop and refine comprehensive quality control standards and inspection protocols for all cleaning services.
- Create detailed checklists and scoring systems for evaluating cleaning performance, hygiene, and safety.
- Conduct remote quality inspections by reviewing detailed reports, photographic evidence, and client feedback from field teams.
- Analyze performance data to identify trends, recurring issues, and areas requiring improvement.
- Collaborate with Area Managers and Site Supervisors to implement corrective action plans and ensure adherence to quality standards.
- Provide constructive feedback and training recommendations to cleaning staff and management teams based on quality assessments.
- Monitor client satisfaction surveys and feedback to gauge service quality and identify areas for enhancement.
- Ensure compliance with health, safety, environmental, and industry-specific regulations.
- Maintain accurate records of quality control inspections, findings, and corrective actions taken.
- Research and recommend innovative tools, technologies, and methods to improve cleaning quality and efficiency.
- Stay updated on the latest cleaning industry standards and best practices.
- Prepare regular quality assurance reports for senior management.
- Act as a point of contact for escalated quality-related issues from clients or operations teams.
Qualifications:
- Bachelor's degree in a relevant field such as Operations Management, Business Administration, or Facilities Management is preferred.
- Minimum of 5 years of experience in quality control, quality assurance, or a related role within the cleaning services, hospitality, or facilities management industry.
- Demonstrated experience in developing and implementing quality management systems.
- Strong understanding of cleaning processes, sanitation standards, and health and safety regulations.
- Excellent analytical and problem-solving skills, with a keen eye for detail.
- Proficiency in data analysis and reporting, preferably with quality management software or tools.
- Exceptional written and verbal communication skills, with the ability to communicate complex information clearly.
- Proven ability to work independently and manage tasks effectively in a remote work environment.
- Experience in remote supervision or auditing is a significant advantage.
- Strong organizational skills and the ability to prioritize effectively.
This position is fully remote, offering the flexibility to work from anywhere. Our client is committed to delivering exceptional cleaning services and maintaining the highest standards. While the company has a strong presence in Nairobi, Nairobi, KE , this role supports operations remotely. Join our client and ensure operational excellence through rigorous quality control.
Remote Quality Control Specialist - Sanitation Standards
Posted 22 days ago
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Job Description
Responsibilities:
- Develop, review, and update cleaning and sanitation policies and procedures.
- Create and deliver comprehensive training programs for cleaning and maintenance staff, conducted virtually.
- Establish and implement rigorous quality control checklists and audit procedures for sanitation services.
- Conduct remote assessments and audits by reviewing submitted reports, photos, and video evidence from on-site teams.
- Monitor adherence to health, safety, and environmental regulations.
- Analyze data from audits and inspections to identify trends, systemic issues, and areas requiring corrective action.
- Recommend and implement improvements to cleaning methodologies, equipment, and supplies.
- Maintain detailed records of audits, training, and corrective actions taken.
- Collaborate with facilities management and operational teams to address sanitation concerns.
- Stay abreast of best practices, new technologies, and regulatory changes in cleaning and sanitation.
- Prepare reports for senior management on sanitation quality and compliance status.
- Troubleshoot and provide guidance on complex sanitation challenges.
Qualifications:
- Bachelor's degree in Environmental Health, Public Health, Biology, Chemistry, or a related field is preferred.
- Proven experience (5+ years) in quality control, sanitation management, or a related role, preferably within a multi-site environment.
- Strong knowledge of cleaning chemicals, disinfection processes, and infection control principles.
- Experience in developing and delivering training programs.
- Excellent auditing and inspection skills, with the ability to assess and report remotely.
- Proficiency in data analysis and report writing.
- Strong understanding of relevant health and safety regulations (e.g., HACCP, OSHA standards where applicable).
- Exceptional communication, interpersonal, and problem-solving skills.
- Ability to work independently and manage time effectively in a remote setting.
- Familiarity with technology platforms for remote auditing and communication is essential.
This remote role is critical for ensuring high standards of cleanliness and safety, supporting operations in areas such as Nakuru, Nakuru, KE and beyond.
Remote Pharmaceutical Research Scientist (Remote)
Posted 22 days ago
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Job Description
Responsibilities:
- Design, execute, and analyze complex experiments related to drug discovery and development in line with project goals.
- Conduct in-depth literature reviews and stay abreast of the latest scientific advancements in relevant therapeutic areas.
- Develop and validate new assays and methodologies to support preclinical and clinical research.
- Interpret experimental data, troubleshoot technical challenges, and propose solutions.
- Prepare detailed reports, scientific manuscripts, and presentations on research findings for internal and external stakeholders.
- Collaborate effectively with cross-functional teams, including chemists, biologists, pharmacologists, and toxicologists, in a virtual environment.
- Ensure strict adherence to laboratory safety protocols, regulatory guidelines (e.g., GLP), and company policies.
- Manage research timelines, resources, and budgets efficiently.
- Contribute to the intellectual property portfolio through patent applications and scientific publications.
- Mentor junior researchers and contribute to a culture of scientific excellence and continuous learning.
- Participate actively in virtual team meetings, scientific seminars, and collaborative discussions.
- Ph.D. in Pharmacology, Biochemistry, Molecular Biology, or a closely related life science discipline.
- Minimum of 5 years of post-doctoral or industry research experience in pharmaceutical R&D.
- Demonstrated expertise in (specific area of expertise, e.g., small molecule drug discovery, biologics development, assay development).
- Strong understanding of drug discovery and development processes.
- Proficiency in relevant experimental techniques and instrumentation.
- Excellent analytical, problem-solving, and critical thinking skills.
- Proven ability to work independently and collaboratively in a remote setting.
- Exceptional written and oral communication skills, with a track record of scientific publication.
- Experience with data analysis software (e.g., GraphPad Prism, R) is highly desirable.
- Familiarity with regulatory requirements in the pharmaceutical industry.
- Must have a stable internet connection and a suitable home office environment conducive to scientific research discussions and data analysis.
- While the role is fully remote, proximity to **Garissa, Garissa, KE** may be beneficial for potential future collaborations or local networking events.
Remote Pharmaceutical Research Scientist
Posted 22 days ago
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Job Description
Key responsibilities include designing and conducting experiments to identify and validate potential drug targets and lead compounds. You will perform in-depth analysis of experimental data, interpret results, and draw scientifically sound conclusions. This involves utilizing a range of laboratory techniques and instrumentation relevant to drug discovery and development, as well as staying abreast of the latest scientific literature and technological advancements in the field.
The Remote Pharmaceutical Research Scientist will be responsible for documenting research activities thoroughly, maintaining accurate laboratory notebooks, and preparing detailed reports on findings. You will collaborate with cross-functional teams, including medicinal chemists, biologists, and pharmacologists, to advance drug candidates through the development pipeline. This involves actively participating in team meetings, contributing to project planning, and presenting research progress and findings.
Further duties may include contributing to the preparation of patent applications, regulatory submissions, and scientific publications. The ideal candidate will possess a Ph.D. or Master's degree in Pharmaceutical Sciences, Pharmacology, Biochemistry, Chemistry, or a related discipline, with a proven track record of research accomplishments in drug discovery. Hands-on experience with relevant research methodologies and analytical techniques is essential. Strong critical thinking, problem-solving skills, and excellent written and oral communication abilities are required. The ability to work independently, manage multiple research projects concurrently, and thrive in a remote, collaborative scientific environment is crucial. This is an exciting opportunity for a dedicated scientist to make a significant impact on pharmaceutical innovation from a remote setting.
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Remote Pharmaceutical Research Associate
Posted 22 days ago
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Job Description
Your Responsibilities Will Include:
- Designing and conducting laboratory experiments or in-silico studies related to drug discovery and development.
- Collecting, analyzing, and interpreting complex research data using statistical software and bioinformatics tools.
- Preparing detailed research reports, manuscripts for publication, and presentations.
- Collaborating with cross-functional teams, including chemists, biologists, and clinicians, in a virtual environment.
- Maintaining accurate and organized records of experimental procedures, results, and observations.
- Ensuring compliance with all relevant regulatory guidelines and company SOPs.
- Troubleshooting experimental issues and developing innovative solutions.
- Contributing to the development of new research methodologies and protocols.
- Staying abreast of the latest scientific literature and advancements in pharmaceutical sciences.
- Presenting research findings at virtual scientific conferences or internal meetings.
- Master's degree or Ph.D. in Pharmacology, Biochemistry, Molecular Biology, Chemistry, or a related life science field.
- Proven experience in pharmaceutical research, with a strong understanding of drug development processes.
- Proficiency in relevant research techniques and methodologies (e.g., cell culture, PCR, Western blotting, chromatography, molecular modeling).
- Strong analytical skills and experience with statistical analysis and data interpretation.
- Excellent written and verbal communication skills, essential for remote collaboration.
- Ability to work independently with minimal supervision and manage multiple projects simultaneously.
- Proficiency in relevant software (e.g., GraphPad Prism, R, Python, Schrödinger Suite).
- A meticulous approach to record-keeping and experimental execution.
- Demonstrated ability to critically evaluate scientific data and draw sound conclusions.
- Experience with regulatory affairs and Good Laboratory Practice (GLP) is a plus.
Remote Sanitation Quality Control Specialist
Posted 22 days ago
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Job Description
Responsibilities:
- Develop and implement comprehensive sanitation quality control protocols.
- Conduct remote audits and inspections of sanitation standards.
- Ensure compliance with all relevant health, safety, and environmental regulations.
- Analyze sanitation data and generate detailed reports on findings and recommendations.
- Provide virtual guidance and training to on-site cleaning teams.
- Identify and document non-compliance issues and develop corrective action plans.
- Maintain accurate and up-to-date sanitation records and documentation.
- Collaborate with management to continuously improve sanitation processes and performance.
- Stay informed about best practices and advancements in sanitation and hygiene.
- Communicate effectively with diverse teams and stakeholders through various digital channels.
- Proven experience in sanitation, quality control, or a related field.
- Strong understanding of hygiene standards and public health regulations.
- Excellent analytical and problem-solving skills.
- Proficiency in using digital tools for reporting, data analysis, and remote collaboration.
- Exceptional written and verbal communication skills.
- Ability to work independently and manage time effectively in a remote setting.
- Attention to detail and commitment to maintaining high standards.
- Experience in developing training materials is a plus.
Remote Pharmaceutical Research Scientist (Computational)
Posted 8 days ago
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Job Description
Responsibilities:
- Perform in silico drug design, virtual screening, and hit-to-lead optimization.
- Apply molecular modeling, docking, and simulation techniques.
- Utilize cheminformatics and bioinformatics tools for data analysis and interpretation.
- Develop and implement machine learning models for predicting drug properties.
- Analyze large datasets from high-throughput screening and omics studies.
- Collaborate with medicinal chemists and biologists on drug discovery projects.
- Contribute to the design of experimental validation studies.
- Prepare high-quality scientific reports, publications, and presentations.
- Stay current with advancements in computational drug discovery and related fields.
- Maintain and manage research databases and computational infrastructure.
- Propose innovative computational approaches to address research challenges.
- Ensure data integrity and reproducibility of computational workflows.
- Mentor junior computational scientists or research associates (as applicable).
- Engage in intellectual property discussions and patent development.
- Contribute to team meetings and strategic planning for drug discovery programs.
- Ph.D. or Master's degree in Computational Chemistry, Bioinformatics, Cheminformatics, Pharmaceutical Sciences, or a related quantitative discipline.
- Proven experience in computational drug discovery within the pharmaceutical industry or academia.
- Proficiency in programming languages such as Python, R, or Java.
- Expertise in molecular modeling software (e.g., Schrodinger, MOE, Discovery Studio) and simulation tools.
- Strong knowledge of biological targets, pharmacology, and drug action mechanisms.
- Experience with large-scale data analysis, databases, and machine learning frameworks.
- Excellent analytical, problem-solving, and critical thinking skills.
- Strong written and verbal communication skills for scientific collaboration.
- Ability to work independently, manage projects, and meet deadlines in a remote environment.
- A strong publication record in peer-reviewed journals is highly desirable.