What Quality Assurance Specialist Jobs are in Ibadan?

Our client, a renowned pharmaceutical company committed to producing high-quality medicines, is seeking a dedicated Quality Assurance Specialist to join their team in Abeokuta, Ogun, NG . This role is essential for maintaining and improving our quality management system, ensuring compliance with regulatory standards, and overseeing all aspects of quality assurance in pharmaceutical operations. The ideal candidate will have a strong understanding of QA principles, experience in the pharmaceutical industry, and a meticulous approach to quality control. This hybrid position offers a blend of in-office collaboration and remote flexibility, providing a balanced work environment. Join a team focused on upholding the highest standards of quality in pharmaceutical production.

• Develop, implement, and maintain the Quality Management System (QMS) in accordance with GMP and other applicable regulations.
• Conduct internal audits and support external audits by regulatory agencies and customers.
• Review and approve batch records, validation protocols, and other quality-related documents.
• Manage deviation investigations, CAPA (Corrective and Preventive Actions), and change control processes.
• Ensure compliance with all relevant regulatory requirements, including local and international pharmaceutical standards.
• Participate in supplier qualification and monitoring activities.
• Train personnel on quality assurance procedures and GMP principles.
• Monitor quality metrics and prepare reports for management review.
• Contribute to the continuous improvement of quality processes and systems.

• Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
• Minimum of 3 years of experience in Quality Assurance within the pharmaceutical industry.
• In-depth knowledge of GMP, ICH guidelines, and regulatory requirements.
• Experience with internal audits, deviation management, and CAPA implementation.
• Strong analytical and problem-solving skills.
• Excellent written and verbal communication skills.
• Proficiency in quality management software and standard office applications.
• Detail-oriented and highly organized.
• Ability to work effectively both independently and as part of a team in a hybrid work environment.

Our client offers a competitive salary and a comprehensive benefits package, including health insurance, retirement plans, and paid time off. The hybrid work model provides flexibility and a good work-life balance. Opportunities for professional development, training, and career advancement within a growing pharmaceutical company are readily available. Join our dedicated quality team in Abeokuta, Ogun, NG and contribute to the delivery of safe and effective medicines.

Our client, a highly respected pharmaceutical company, is seeking an innovative Pharmaceutical Formulation Scientist to contribute to their drug development efforts in Ibadan . This role focuses on the design, development, and optimization of drug delivery systems and dosage forms for novel and existing pharmaceutical products. The successful candidate will possess a strong understanding of pharmaceutics, drug delivery technologies, and pre-formulation studies. You will be instrumental in translating scientific concepts into viable, patient-friendly formulations. This is an exciting opportunity to work in a cutting-edge research environment and influence the future of our client's product pipeline. The role demands creativity, analytical rigor, and a collaborative spirit, working closely with various R&D departments. Embrace the challenge of developing effective and stable pharmaceutical formulations from your remote workspace, serving the innovation needs of our client.

• Design and develop various dosage forms, including oral solids, liquids, and sterile preparations.
• Conduct pre-formulation studies to characterize drug substances and excipients.
• Optimize formulations for stability, bioavailability, and manufacturability.
• Perform laboratory experiments, analyze data, and document findings comprehensively.
• Develop and validate analytical methods for formulation characterization.
• Troubleshoot formulation-related issues during development and scale-up.
• Collaborate with analytical development, process chemistry, and manufacturing teams.
• Stay current with emerging trends and technologies in pharmaceutical formulation and drug delivery.
• Prepare technical reports and contribute to regulatory filings.

• Master's or Ph.D. degree in Pharmaceutical Sciences, Pharmaceutics, Chemical Engineering, or a related field.
• Minimum of 4-6 years of experience in pharmaceutical formulation development.
• Proven experience with a range of dosage forms and drug delivery systems.
• Strong understanding of physical chemistry, material science, and biopharmaceutics.
• Proficiency in laboratory techniques and equipment used in formulation development.
• Excellent data analysis and interpretation skills.
• Strong written and verbal communication abilities.
• Experience with statistical software and design of experiments (DoE) is advantageous.

This position offers a competitive salary, comprehensive health benefits, and opportunities for professional growth within a dynamic and supportive organization. As a remote role, it provides significant flexibility and work-life balance. Our client is committed to fostering an environment where scientific curiosity and innovation thrive, allowing you to make a meaningful impact on healthcare from wherever you work best, while supporting operations relevant to Ibadan .

• Develop, optimize, and validate analytical methods (e.g., HPLC, GC, UV-Vis, KF) for raw materials, intermediates, and finished drug products.
• Perform routine quality control testing according to established protocols and regulatory guidelines.
• Investigate and troubleshoot analytical method deviations and out-of-specification results.
• Characterize drug substances and drug products, including purity, potency, and dissolution testing.
• Prepare detailed analytical reports, method validation protocols, and validation reports.
• Ensure compliance with Good Manufacturing Practices (GMP) and other relevant regulatory standards.
• Operate and maintain analytical instrumentation, ensuring proper calibration and performance.
• Collaborate with formulation scientists, process chemists, and quality assurance personnel.
• Stay updated on current trends and advancements in pharmaceutical analytical chemistry.
• Mentor junior analytical chemists and provide technical guidance.

• Master's or PhD degree in Analytical Chemistry, Pharmaceutical Sciences, or a related field.
• Minimum of 5 years of hands-on experience in pharmaceutical analytical development and quality control.
• Proficiency with chromatographic techniques such as HPLC, UPLC, and GC, including method development and validation.
• Experience with spectroscopic techniques (e.g., UV-Vis, FTIR) and wet chemistry methods.
• Thorough understanding of pharmaceutical regulatory guidelines (e.g., ICH, FDA, EMA).
• Experience with stability testing programs and data analysis.
• Strong analytical and problem-solving skills with meticulous attention to detail.
• Excellent written and verbal communication skills.
• Ability to manage multiple projects and prioritize tasks effectively.
• Experience with Mass Spectrometry (MS) is a plus.

• Design and synthesize novel small molecules with potential therapeutic activity using a range of modern organic chemistry techniques.
• Optimize lead compounds through iterative cycles of synthesis and biological testing to improve potency, selectivity, and pharmacokinetic properties.
• Characterize synthesized compounds using analytical techniques such as NMR, Mass Spectrometry, HPLC, and LC-MS.
• Collaborate closely with biologists, pharmacologists, and other scientists to design and interpret experimental results and guide SAR studies.
• Develop efficient and scalable synthetic routes for promising drug candidates.
• Maintain detailed and accurate laboratory notebooks and prepare scientific reports and presentations.
• Stay abreast of the latest advancements in medicinal chemistry, synthetic methodologies, and drug discovery trends.
• Contribute to the intellectual property strategy by identifying patentable inventions.
• Participate in team meetings, project reviews, and scientific discussions.
• Ensure adherence to laboratory safety protocols and best practices.

• Ph.D. in Organic Chemistry, Medicinal Chemistry, or a closely related field.
• A minimum of 3-5 years of postdoctoral or industry experience in drug discovery and medicinal chemistry.
• Proven track record of synthesizing and characterizing novel small molecules.
• Extensive knowledge of modern synthetic organic chemistry techniques and reaction mechanisms.
• Experience with SAR exploration and lead optimization strategies.
• Proficiency in using analytical instrumentation (NMR, MS, HPLC) for compound characterization.
• Familiarity with computational chemistry tools and techniques is a plus.
• Strong problem-solving abilities and excellent scientific judgment.
• Effective written and verbal communication skills for reporting findings and collaborating with team members.
• Ability to work independently and contribute effectively within a multidisciplinary research team.

• Competitive salary and potential for performance-based bonuses.
• Comprehensive health, dental, and vision insurance.
• Generous paid time off and holidays.
• Opportunities for professional development and attendance at scientific conferences.
• Retirement savings plan.
• Life insurance.
• Access to cutting-edge research facilities and equipment.
• A collaborative and stimulating scientific environment.
• Support for career growth and advancement.
• Employee wellness programs.

NHC Pharmaceuticals Limited is a Pharma wholesales distribution company that is dedicated to empowering healthcare providers by bridging supply gaps. With branches across multiple states in Western Nigeria, we ensure that pharmacies, hospitals and other healthcare institutions have access to essential healthcare products through reliable and efficient service. We are more than just a supplier; we’re a trusted partner, helping healthcare providers meet their patients’ needs with confidence.

• Design and execute laboratory experiments to develop and optimize chemical synthesis routes for active pharmaceutical ingredients (APIs) and intermediates.
• Perform process characterization studies, including reaction kinetics, impurity profiling, and polymorph screening.
• Develop robust and scalable processes suitable for pilot plant and commercial manufacturing.
• Operate and troubleshoot laboratory and pilot-scale equipment.
• Analyze experimental data using statistical methods and interpret results to guide process improvements.
• Prepare technical reports, research summaries, and process documentation.
• Collaborate with analytical development, formulation, and manufacturing teams to ensure successful process transfer and implementation.
• Conduct risk assessments and implement appropriate safety measures for all experimental procedures.
• Stay current with advancements in synthetic organic chemistry, process chemistry, and chemical engineering.
• Contribute to intellectual property generation through novel process development.

• PhD or Master's degree in Organic Chemistry, Chemical Engineering, or a related field with a strong emphasis on process development.
• Minimum of 4 years of hands-on experience in chemical process development, preferably in the pharmaceutical or fine chemicals industry.
• Proficiency in synthetic organic chemistry techniques and laboratory practices.
• Experience with process analytical technology (PAT) and design of experiments (DoE) is highly desirable.
• Strong understanding of chemical engineering principles related to scale-up, thermodynamics, and mass transfer.
• Experience with analytical techniques such as HPLC, GC, MS, NMR, and KF titration.
• Excellent data analysis, documentation, and technical writing skills.
• Ability to work effectively both independently and as part of a multidisciplinary team.
• Good communication skills for reporting findings and collaborating with colleagues.
• Must be able to commute to Ibadan, Oyo, NG for hybrid work requirements.

• Competitive annual salary of NGN.
• Hybrid work model offering flexibility.
• Comprehensive health, dental, and vision insurance.
• Performance-based annual bonus.
• Generous paid time off and company holidays.
• Support for professional development, including conference attendance.
• Retirement savings plan.
• Access to cutting-edge laboratory facilities and equipment.
• Employee assistance program.
• Opportunity to contribute to life-changing pharmaceutical products.

Our client, a significant operator in the Oil & Gas sector, is seeking a skilled Production Chemist Specialist to join their team in Ibadan, Oyo, Nigeria . This role is integral to optimizing production processes by ensuring the effective management and application of production chemicals. You will be responsible for the technical evaluation, selection, and monitoring of chemicals used in upstream operations, aiming to enhance oil and gas recovery, prevent corrosion, and mitigate scale formation. This hybrid position requires a blend of laboratory analysis, field support, and technical consultation. The ideal candidate possesses a strong understanding of production chemistry, emulsion breaking, hydrate inhibition, and flow assurance. You will work closely with production engineers and operations teams to troubleshoot issues and implement chemical solutions that improve asset performance and longevity. This is a great opportunity to make a tangible impact on operational efficiency and hydrocarbon recovery.

• Develop and implement chemical management programs for production facilities.
• Conduct laboratory analysis to evaluate the performance of production chemicals (e.g., corrosion inhibitors, scale inhibitors, demulsifiers, biocides).
• Troubleshoot production chemistry-related issues, identifying root causes and recommending appropriate solutions.
• Monitor chemical injection rates, concentrations, and system effectiveness.
• Collaborate with production engineers to optimize chemical treatment strategies for wells and facilities.
• Review and recommend new chemical technologies and vendors.
• Ensure compliance with chemical handling, storage, and disposal regulations.
• Prepare technical reports on chemical performance, system integrity, and recommendations for improvement.
• Participate in field visits to production sites to provide technical support and gather operational data.

• Bachelor's degree in Chemistry, Chemical Engineering, or a related field.
• Minimum of 5 years of experience in production chemistry within the Oil & Gas industry, preferably with experience in Nigerian operational environments.
• Strong knowledge of hydrocarbon production processes and associated chemical challenges.
• Hands-on experience with laboratory testing of production chemicals.
• Familiarity with corrosion, scale, and emulsion control principles.
• Understanding of flow assurance principles and hydrate management is a plus.
• Good analytical and problem-solving skills.
• Effective communication and interpersonal skills for collaborating with multidisciplinary teams.
• Ability to interpret technical data and generate clear, concise reports.
• Proficiency in relevant software for data analysis and reporting.

Our client offers a competitive salary, comprehensive health and wellness benefits, and retirement savings plan. This hybrid role provides a balance between working from home and in the office in Ibadan . Opportunities for professional development, including specialized training courses and participation in industry forums, are available. Employees benefit from paid time off and a supportive work environment that encourages collaboration and innovation within the Oil & Gas sector. The company is committed to operational excellence and employee growth, making this a rewarding career opportunity.

• Perform a wide range of analytical tests on raw materials, in-process samples, and finished products using techniques such as HPLC, GC, UV-Vis, FTIR, and titrations.
• Develop, validate, and transfer analytical methods according to ICH guidelines and regulatory requirements.
• Calibrate and maintain laboratory equipment, ensuring optimal performance and accuracy.
• Troubleshoot analytical methods and instrumentation issues.
• Review and approve analytical data, ensuring accuracy, completeness, and compliance with specifications.
• Prepare detailed analytical reports, certificates of analysis, and other required documentation.
• Participate in stability studies, including sample management and data analysis.
• Ensure all laboratory activities are conducted in compliance with GMP and GLP standards.
• Train and mentor junior analysts in laboratory techniques and procedures.
• Contribute to the continuous improvement of laboratory operations and quality systems.

• Bachelor's or Master's degree in Chemistry, Pharmaceutical Chemistry, Analytical Chemistry, or a related scientific discipline.
• A minimum of 6 years of hands-on experience in a pharmaceutical Quality Control laboratory setting.
• Extensive experience with HPLC and GC is essential; knowledge of other spectroscopic techniques is highly desirable.
• Proficiency in method development and validation according to ICH guidelines.
• Strong understanding of GMP regulations and pharmacopeial standards (e.g., USP, EP).
• Excellent analytical, problem-solving, and troubleshooting skills.
• Meticulous attention to detail and strong documentation practices.
• Ability to work effectively both independently and as part of a collaborative team in **Ibadan**.
• Good communication skills, both written and verbal.
• Experience with LIMS (Laboratory Information Management System) is a plus.

• Competitive salary based on experience and qualifications.
• Comprehensive health and wellness benefits package.
• Opportunities for professional growth and advancement within the company.
• Access to advanced analytical instrumentation and technology.
• A supportive and collaborative laboratory environment in **Ibadan**.
• Contribution to the development and production of life-saving medicines.
• Paid time off and annual leave.

• Prepare, review, and submit regulatory dossiers (e.g., CTD, NDA, ANDA) to health authorities.
• Ensure compliance with local and international regulatory guidelines, including GMP, GCP, and GLP.
• Manage the lifecycle of regulatory submissions, including post-approval variations and annual reports.
• Liaise with regulatory agencies, respond to queries, and facilitate inspections.
• Provide regulatory guidance and support to internal departments, including R&D, manufacturing, and marketing.
• Monitor changes in regulatory requirements and assess their impact on company products and processes.
• Maintain regulatory databases and ensure accurate record-keeping of all submissions and approvals.
• Conduct regulatory intelligence activities to stay informed about global regulatory trends and requirements.
• Review product labeling and promotional materials for regulatory compliance.

• Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science field.
• Minimum of 4 years of experience in pharmaceutical regulatory affairs.
• Proven experience in preparing and submitting regulatory dossiers to health authorities.
• In-depth knowledge of pharmaceutical regulations (e.g., FDA, EMA, NAFDAC) and guidelines.
• Strong understanding of drug development processes and manufacturing.
• Excellent written and verbal communication skills, with strong attention to detail.
• Ability to work independently and manage multiple projects in a fast-paced environment.
• Proficiency in regulatory affairs software and documentation management systems is preferred.
• Strong analytical and problem-solving skills.