What Senior Analytical Chemist Quality Control Jobs are in Nigeria?

• Develop, validate, and transfer analytical methods for raw materials, in-process samples, and finished pharmaceutical products.
• Perform routine and non-routine analyses using techniques such as HPLC, GC, UV-Vis, FTIR, and dissolution testing.
• Analyze and interpret analytical data, identify deviations, and investigate out-of-specification (OOS) results.
• Ensure all analytical activities comply with Good Manufacturing Practices (GMP) and other relevant regulatory guidelines.
• Maintain laboratory equipment, perform calibrations, and ensure proper functioning of analytical instruments.
• Prepare and review analytical reports, method validation protocols, and stability study reports.
• Troubleshoot analytical methods and instrumentation issues.
• Train and mentor junior analytical chemists and technicians.
• Collaborate with formulation development, manufacturing, and regulatory affairs teams.
• Stay current with advancements in analytical chemistry and pharmaceutical quality control.

• M.Sc. or Ph.D. in Analytical Chemistry, Pharmaceutical Chemistry, or a related scientific discipline.
• Minimum of 5-7 years of relevant experience in analytical chemistry, specifically within the pharmaceutical industry.
• Proficiency with analytical instrumentation such as HPLC, GC, Mass Spectrometry (MS), UV-Vis, and dissolution apparatus.
• Strong understanding of pharmaceutical quality control principles and GMP regulations.
• Experience in method development, validation, and transfer.
• Excellent data interpretation and problem-solving skills.
• Strong written and verbal communication skills.
• Ability to manage multiple priorities and work effectively under pressure.
• Attention to detail and commitment to maintaining high-quality standards.
• Must be legally eligible to work in **Nigeria**.

Our client, a globally recognized pharmaceutical manufacturer, is seeking a dedicated and experienced Senior Microbiologist to join their Quality Assurance team in **Zaria, Kaduna, NG**. This vital role will focus on overseeing and executing microbiological testing, environmental monitoring, and ensuring compliance with stringent pharmaceutical quality standards. The ideal candidate will possess a deep understanding of microbial detection, identification, and control strategies within a GMP environment. This is a hands-on position that requires meticulous attention to detail and a strong commitment to patient safety. The successful applicant will play a crucial role in safeguarding product integrity and upholding the company's reputation for excellence. This role is critical for maintaining the highest standards of quality in our pharmaceutical production.

• Perform and interpret a wide range of microbiological tests on raw materials, in-process samples, finished products, and facility environments.
• Conduct environmental monitoring (air, surface, water) of manufacturing areas and report on trends and deviations.
• Develop, validate, and implement new microbiological methods and assays according to pharmacopeial and regulatory guidelines.
• Investigate and troubleshoot microbial contamination excursions, identifying root causes and implementing corrective and preventive actions (CAPAs).
• Maintain accurate and detailed records of all testing performed, ensuring compliance with GMP documentation requirements.
• Ensure the proper functioning, calibration, and maintenance of microbiological laboratory equipment.
• Stay updated on the latest developments in microbiology, sterilization techniques, and regulatory requirements relevant to the pharmaceutical industry.
• Collaborate effectively with Quality Control, Production, and Validation teams to ensure product quality and compliance.
• Train and mentor junior microbiologists and laboratory technicians.
• Participate in internal and external audits as a subject matter expert.

• M.Sc. or Ph.D. in Microbiology, Biology, Biotechnology, or a related life science field.
• Minimum of 5 years of progressive experience in pharmaceutical microbiology, with a strong focus on quality control/assurance.
• Proven expertise in microbial identification, sterility testing, endotoxin testing (LAL), and microbial limit testing.
• Comprehensive understanding of GMP, ISO standards, and relevant pharmacopeias (e.g., USP, EP).
• Experience with environmental monitoring programs and cleanroom classifications.
• Proficiency in aseptic techniques and relevant laboratory safety practices.
• Strong analytical and problem-solving skills.
• Excellent written and verbal communication skills, with experience in report writing and documentation.
• Ability to work independently and effectively within a team-oriented environment.
• Demonstrated leadership potential and mentoring experience.

Our client offers a competitive salary and benefits package, including comprehensive health insurance, retirement plans, and paid time off. Opportunities for professional growth are provided through training programs, workshops, and support for attending scientific conferences. Employees have access to state-of-the-art laboratory facilities and advanced scientific equipment. We foster a culture of teamwork, scientific rigor, and continuous improvement. This on-site position is based in **Zaria, Kaduna, NG**, offering a stable and rewarding career in pharmaceutical quality assurance.

• Perform routine and non-routine analytical testing on raw materials, in-process samples, and finished products using various laboratory techniques and instrumentation.
• Ensure all testing is conducted according to established Standard Operating Procedures (SOPs) and quality guidelines.
• Calibrate and maintain laboratory equipment, ensuring accuracy and reliability of test results.
• Accurately document all test results, maintain detailed records, and prepare Certificates of Analysis (CoAs).
• Troubleshoot analytical methods and equipment issues, escalating as necessary.
• Collaborate with production and R&D teams to address quality deviations and implement corrective actions.
• Participate in internal quality audits and assist with external regulatory inspections.
• Maintain a clean and safe laboratory environment, adhering to all safety protocols.
• Contribute to the continuous improvement of quality control processes and procedures.

• Bachelor's degree in Chemistry, Chemical Technology, or a related scientific field.
• A minimum of 3 years of experience in a Quality Control or Quality Assurance role within the chemical manufacturing industry.
• Proficiency in various analytical techniques such as HPLC, GC, UV-Vis spectrophotometry, titrations, and Karl Fischer.
• Experience with laboratory information management systems (LIMS) is a plus.
• Strong understanding of Good Laboratory Practices (GLP) and quality management systems (e.g., ISO 9001).
• Excellent attention to detail and accuracy in data recording and analysis.
• Good organizational and time management skills, with the ability to manage multiple tasks efficiently.
• Effective communication and teamwork skills.
• Ability to work effectively in a laboratory setting in **Gombe, Gombe, NG**.

• Perform a wide range of microbiological tests on raw materials, in-process samples, and finished products.
• Develop and validate new microbiological testing methods according to USP, EP, and other relevant pharmacopeial standards.
• Conduct environmental monitoring of manufacturing areas and cleanrooms.
• Investigate microbial contamination investigations, identifying root causes and implementing corrective actions.
• Manage laboratory inventory, equipment calibration, and maintenance.
• Ensure compliance with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).
• Train and mentor junior laboratory personnel.
• Prepare reports, documentation, and support for regulatory submissions.
• Stay current with advancements in microbiology and relevant regulatory guidelines.
• Participate in internal and external audits.

• Master's or Ph.D. in Microbiology, Biology, or a related scientific field.
• Minimum of 5 years of experience in pharmaceutical or medical device quality control microbiology.
• Extensive knowledge of compendial methods (USP, EP) for microbiological testing.
• Hands-on experience with techniques such as microbial enumeration, sterility testing, bioburden analysis, and microbial identification.
• Experience with environmental monitoring programs and cleanroom classifications.
• Proficiency in aseptic techniques and microbial culture handling.
• Strong understanding of GMP regulations and quality systems.
• Excellent analytical, problem-solving, and troubleshooting skills.
• Strong communication and leadership abilities.
• Experience with data integrity principles and laboratory information management systems (LIMS) is a plus.

• Competitive salary and benefits package.
• Annual performance bonus.
• Opportunities for professional development and career growth.
• State-of-the-art microbiological laboratory facilities in **Abeokuta, Ogun**.
• Health, dental, and vision insurance.
• Generous paid time off.
• Retirement savings plan.
• A collaborative and quality-focused work environment.

• Develop, implement, and maintain quality assurance programs and procedures in accordance with regulatory guidelines (e.g., GMP, ICH).
• Conduct internal audits and inspections of manufacturing processes, documentation, and facilities to ensure compliance.
• Investigate deviations, CAPAs (Corrective and Preventive Actions), and change controls, ensuring thorough root cause analysis and effective implementation of resolutions.
• Review and approve batch records, validation protocols, and other critical quality documents.
• Monitor and analyze quality control data, identifying trends and implementing necessary improvements.
• Collaborate with cross-functional teams, including R&D, manufacturing, and regulatory affairs, to ensure quality objectives are met.
• Prepare and host external audits by regulatory authorities and partners.
• Contribute to the continuous improvement of the Quality Management System (QMS).
• Stay abreast of evolving regulatory requirements and industry best practices.

• Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field. A Master's degree is a plus.
• Minimum of 5 years of progressive experience in Quality Assurance within the pharmaceutical industry.
• In-depth knowledge of pharmaceutical manufacturing processes, GMP, and relevant regulatory frameworks.
• Proven experience in conducting audits, investigating deviations, and managing CAPAs.
• Strong analytical and problem-solving skills with meticulous attention to detail.
• Excellent written and verbal communication skills, with the ability to articulate complex quality issues clearly.
• Proficiency in using quality management software and standard office applications.
• Ability to work independently and manage multiple priorities in a remote setting.
• Demonstrated ability to collaborate effectively with remote teams.

Our client, a leading pharmaceutical manufacturer renowned for its commitment to quality and innovation, is seeking a seasoned Senior Pharmaceutical QA/QC Manager to lead their quality assurance and quality control operations in Makurdi, Benue, NG . This pivotal role demands a strategic leader responsible for establishing, maintaining, and continuously improving the company's Quality Management System (QMS). You will ensure that all products meet the highest standards of safety, efficacy, and compliance with national and international regulatory requirements, including GMP. The ideal candidate possesses extensive experience in pharmaceutical quality assurance and control, a deep understanding of regulatory landscapes, and exceptional leadership and problem-solving skills. This is a significant opportunity to shape the quality culture of a respected organization and contribute to the delivery of life-saving medications. The work environment is dynamic and demanding, offering substantial responsibility and opportunities for professional growth. You will oversee both laboratory operations and strategic quality initiatives, ensuring that quality is embedded in every aspect of the manufacturing process. We are looking for a candidate with a proactive approach and a meticulous attention to detail.

• Develop, implement, and manage the company's Quality Management System (QMS) to ensure compliance with GMP and other relevant regulations.
• Oversee all Quality Control (QC) laboratory activities, including raw material testing, in-process testing, and finished product release testing.
• Lead the Quality Assurance (QA) functions, including batch record review, deviation management, change control, CAPA implementation, and internal/external audits.
• Ensure compliance with NAFDAC regulations and other applicable international standards.
• Manage and mentor the QA/QC team, fostering a culture of quality and continuous improvement.
• Develop and implement quality training programs for all relevant personnel.
• Review and approve validation protocols and reports for manufacturing processes and analytical methods.
• Act as the primary point of contact for regulatory agency inspections and audits.
• Investigate quality complaints and deviations, determining root causes and implementing effective corrective and preventive actions.
• Drive continuous improvement initiatives to enhance product quality, process efficiency, and regulatory compliance.

• Bachelor's degree in Pharmacy, Chemistry, Microbiology, or a related life science discipline. Master's degree preferred.
• Minimum of 8 years of progressive experience in pharmaceutical Quality Assurance and Quality Control, with at least 3 years in a management role.
• In-depth knowledge of GMP, regulatory requirements (NAFDAC, FDA, EMA), and quality systems.
• Proven experience in managing QA/QC operations, including laboratory oversight, batch release, validation, and audits.
• Strong leadership, communication, problem-solving, and decision-making skills.
• Excellent understanding of pharmaceutical manufacturing processes.
• Ability to develop and implement strategic quality initiatives.
• Proficiency in quality risk management and continuous improvement methodologies.
• Must be based in or willing to relocate to Makurdi, Benue, NG .

Our client offers a highly competitive salary, a comprehensive benefits package including health insurance, life insurance, and a robust retirement savings plan. Employees receive generous paid annual leave and excellent opportunities for professional development, including advanced training, certifications, and attendance at key industry conferences. The company provides access to modern facilities and fosters a culture of excellence, collaboration, and innovation. Opportunities for career advancement within a respected pharmaceutical organization are significant. The company is committed to employee well-being and work-life balance. Performance-based bonuses are also provided.

• Develop, validate, and implement analytical methods for testing pharmaceutical ingredients and products using techniques like HPLC, GC, UV-Vis, FTIR, and dissolution testing.
• Perform routine quality control testing on raw materials, intermediates, and finished dosage forms.
• Analyze samples to determine purity, potency, and identity according to established specifications and pharmacopeial standards (e.g., USP, BP).
• Investigate out-of-specification (OOS) results, identify root causes, and implement corrective and preventive actions (CAPAs).
• Maintain and calibrate analytical laboratory instruments to ensure accurate and reliable results.
• Prepare and review analytical test reports, batch records, and validation documents.
• Ensure all laboratory activities comply with Good Manufacturing Practices (GMP) and other relevant regulatory guidelines.
• Train and mentor junior analytical chemists and technicians.
• Stay current with advances in analytical chemistry techniques and regulatory expectations.

• Bachelor's or Master's degree in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or a related field.
• Minimum of 5 years of experience in analytical chemistry within the pharmaceutical industry, with a focus on Quality Control (QC).
• Extensive hands-on experience with analytical instruments such as HPLC, GC, Mass Spectrometry, UV-Vis, and FTIR.
• Strong knowledge of method development, validation, and transfer procedures.
• Familiarity with pharmacopeias (USP, BP, EP) and GMP guidelines.
• Excellent analytical and problem-solving skills, with meticulous attention to detail.
• Proficiency in data analysis and interpretation, including statistical analysis.
• Strong written and verbal communication skills.
• Ability to work effectively in a fast-paced laboratory environment.

• Competitive salary and performance-based bonuses.
• Comprehensive health, dental, and vision insurance.
• Retirement savings plan with company contribution.
• Generous paid vacation and sick leave.
• Opportunities for professional development and continuing education.
• Access to modern analytical instrumentation and laboratory facilities.
• Stable and secure employment within a reputable company.
• Career advancement opportunities within the quality assurance/quality control departments.

Our client, a dynamic and growing pharmaceutical company, is looking for an accomplished Pharmaceutical Quality Control Manager to lead their quality assurance efforts in Ilorin, Kwara, NG . This critical role is responsible for ensuring that all manufactured pharmaceutical products meet stringent quality standards and regulatory requirements. The ideal candidate will have a deep understanding of Good Manufacturing Practices (GMP) and extensive experience in quality control methodologies within the pharmaceutical sector. You will oversee a team of quality control analysts, manage laboratory operations, and implement robust quality systems. This position offers a significant opportunity to shape the quality framework of a reputable organization. We are committed to upholding the highest standards of product quality and patient safety, and this role is central to achieving those goals. The successful candidate will be instrumental in maintaining our client's reputation for excellence and compliance. If you are a detail-oriented leader with a passion for quality, this role is for you.

• Develop, implement, and manage comprehensive quality control programs and procedures.
• Oversee the day-to-day operations of the quality control laboratory, including sample testing and data analysis.
• Ensure compliance with all relevant regulatory standards, including GMP, ICH guidelines, and local health authority regulations.
• Manage and mentor a team of quality control analysts, providing training and performance evaluations.
• Review and approve batch records, validation protocols, and stability studies.
• Investigate deviations, out-of-specification (OOS) results, and customer complaints, implementing corrective and preventive actions (CAPAs).
• Collaborate with production, R&D, and regulatory affairs departments to resolve quality issues and ensure product integrity.
• Manage external audits from regulatory agencies and customers.
• Maintain laboratory equipment and ensure proper calibration and qualification.
• Contribute to continuous improvement initiatives within the quality management system.

• Master's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
• Minimum of 8 years of progressive experience in pharmaceutical quality control or quality assurance.
• At least 3 years of experience in a supervisory or managerial role.
• In-depth knowledge of GMP, ICH guidelines, and other relevant regulatory requirements.
• Proven experience with analytical testing methods (e.g., HPLC, GC, spectroscopy) and laboratory instrumentation.
• Strong understanding of quality management systems, validation, and stability programs.
• Excellent leadership, team management, and communication skills.
• Proficiency in data analysis and report writing.
• Ability to work effectively under pressure and meet deadlines.
• Detail-oriented with a strong commitment to quality and compliance.

• Competitive salary and performance-based bonuses.
• Comprehensive medical, dental, and vision coverage.
• Generous vacation and sick leave policy.
• Opportunities for professional growth and leadership development.
• A collaborative and supportive work environment in Ilorin, Kwara, NG .
• Retirement savings plan.
• Company-provided training and certifications.
• Access to modern laboratory facilities.
• Potential for career advancement within a growing organization.
• Employee assistance program.

Our client, a rapidly expanding pharmaceutical company, is seeking a dedicated and experienced Quality Control Manager to oversee all quality assurance and control operations at their state-of-the-art facility located in Ado-Ekiti, Ekiti, NG . This critical role ensures that all products meet the highest standards of safety, efficacy, and regulatory compliance. The ideal candidate will possess a deep understanding of pharmaceutical manufacturing processes, quality management systems, and relevant regulatory frameworks. This is a hands-on leadership position for someone passionate about maintaining product integrity and driving continuous improvement within a vital sector of the healthcare industry. You will be a key figure in upholding the company's commitment to excellence and patient safety.

• Develop, implement, and maintain a comprehensive Quality Management System (QMS) in compliance with Good Manufacturing Practices (GMP) and other relevant regulations.
• Supervise and lead the Quality Control laboratory team, including chemists, analysts, and technicians.
• Establish and manage testing protocols for raw materials, in-process samples, and finished pharmaceutical products.
• Review and approve batch records, analytical data, and Certificates of Analysis (CoA).
• Investigate deviations, out-of-specification (OOS) results, and customer complaints, implementing robust corrective and preventive actions (CAPA).
• Conduct internal audits and support external regulatory inspections.
• Oversee equipment calibration, validation, and maintenance programs for the QC laboratory.
• Train QC personnel on testing procedures, GMP, and safety protocols.

• Master's degree or PhD in Chemistry, Pharmacy, Microbiology, or a related scientific discipline.
• Minimum of 7 years of progressive experience in pharmaceutical quality control and quality assurance.
• At least 3 years of experience in a managerial or supervisory role within a pharmaceutical QC environment.
• Extensive knowledge of GMP, regulatory guidelines (e.g., NAFDAC, WHO), and pharmacopeial standards.
• Proven experience in method development, validation, and transfer.
• Strong leadership, communication, and problem-solving skills.
• Experience with analytical instrumentation (e.g., HPLC, GC, UV-Vis, FTIR).
• Ability to work effectively under pressure and manage multiple priorities in a fast-paced manufacturing setting in Ado-Ekiti .

Our client offers a competitive remuneration package, including a strong base salary and performance-based bonuses. You will be eligible for a comprehensive benefits program, including health insurance, retirement contributions, and paid time off. Opportunities for professional development and continuous learning will be provided. The role offers significant influence over quality operations and career progression within a growing organization. Join our team in Ado-Ekiti, Ekiti, NG and contribute to the production of high-quality pharmaceutical products.