5,885 Pharmaceutical Quality Control Analyst jobs in Kenya
Pharmaceutical Quality Control Specialist
Posted 13 days ago
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Job Description
Our client is seeking a highly meticulous and diligent Pharmaceutical Quality Control Specialist to uphold the highest standards of product integrity within their operations, operating in a fully remote capacity. This role is vital in ensuring that all pharmaceutical products meet rigorous quality specifications and regulatory requirements. The ideal candidate will possess a strong understanding of pharmaceutical manufacturing processes, quality assurance principles, and relevant regulatory guidelines (e.g., GMP, ICH). You will be responsible for reviewing and analyzing batch records, conducting laboratory data analysis, and performing validation testing. This position requires exceptional attention to detail, strong analytical skills, and the ability to interpret scientific data accurately in a remote environment. Key responsibilities include identifying deviations from quality standards, participating in investigations of quality issues, and contributing to the continuous improvement of quality systems. You will collaborate with R&D, manufacturing, and regulatory affairs teams to ensure product quality throughout its lifecycle. We are looking for a candidate with a Bachelor's degree in a relevant scientific field (e.g., Pharmacy, Chemistry, Biotechnology) and a proven track record in pharmaceutical quality control. If you are a proactive professional committed to ensuring patient safety and product efficacy, and seeking a rewarding remote career, we encourage you to apply. Your home office will serve as your operational base, requiring a stable internet connection for accessing quality management systems and collaborating with colleagues. This role offers a competitive salary and the opportunity to contribute to the development and manufacturing of essential medicines. Your dedication to quality assurance will be paramount in safeguarding public health and maintaining our client's reputation for excellence.
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Remote Pharmaceutical Quality Control Specialist
Posted 22 days ago
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Job Description
Our client, a rapidly expanding pharmaceutical company, is actively seeking a meticulous and experienced Pharmaceutical Quality Control Specialist to join their team. This is a fully remote position, allowing you to contribute to critical quality assurance processes from anywhere. The ideal candidate will possess a strong understanding of Good Manufacturing Practices (GMP), quality management systems, and regulatory requirements within the pharmaceutical industry. You will be responsible for reviewing and analyzing laboratory data, ensuring that raw materials, in-process samples, and finished products meet stringent quality specifications and regulatory standards. This involves executing various analytical tests, interpreting results, and documenting all activities in accordance with established protocols. Your role will include performing stability studies, investigating out-of-specification (OOS) results, and contributing to the development and validation of analytical methods. You will collaborate with cross-functional teams, including R&D, manufacturing, and regulatory affairs, to ensure product quality and compliance throughout the product lifecycle. A key aspect of this role involves maintaining detailed and accurate records, preparing quality control reports, and participating in internal and external audits. A Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field is essential, along with a minimum of 4 years of progressive experience in pharmaceutical quality control or quality assurance. Hands-on experience with analytical instrumentation (e.g., HPLC, GC, UV-Vis spectrophotometry) and familiarity with relevant pharmacopeias (e.g., USP, EP) are required. Excellent analytical, problem-solving, and documentation skills are paramount. The ability to work independently, manage multiple tasks efficiently, and adhere strictly to deadlines in a remote setting is crucial. This role offers a fantastic opportunity to contribute to the development and delivery of safe and effective pharmaceutical products while enjoying the benefits of a remote work environment. The position is designated for individuals interested in the **Kakamega, Kakamega, KE** area, with the work conducted entirely remotely.
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Senior Pharmaceutical Quality Control Specialist
Posted 15 days ago
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Job Description
Our client is seeking a highly qualified Senior Pharmaceutical Quality Control Specialist to ensure the highest standards of pharmaceutical product quality. This is a fully remote position, allowing you to contribute your expertise from any location. You will be responsible for designing and implementing robust quality control protocols, analyzing raw materials and finished products, and ensuring compliance with regulatory requirements. Your duties will include performing analytical testing, validating testing methods, documenting quality control procedures, and investigating deviations from quality standards. The ideal candidate will have a strong background in pharmaceutical sciences, with extensive experience in quality assurance and quality control within the pharmaceutical industry. Proficiency in analytical techniques such as HPLC, GC, and spectroscopy is essential. You should possess exceptional attention to detail, strong problem-solving skills, and a thorough understanding of Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP). Experience with regulatory submissions and audits is highly desirable. This role offers an exciting opportunity to make a significant impact on patient safety and product efficacy, all within a flexible remote work arrangement. You will be a key player in upholding our client's commitment to quality and regulatory excellence. We are looking for a dedicated professional who can maintain meticulous records and drive continuous improvement in quality processes. This is an ideal role for a seasoned specialist looking for a senior-level remote opportunity, contributing to the pharmaceutical sector from the heart of Kakamega, Kakamega, KE .
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Remote Senior Pharmaceutical Quality Control Specialist
Posted 22 days ago
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Job Description
Our client, a reputable pharmaceutical manufacturing organization, is seeking a highly diligent and experienced Senior Pharmaceutical Quality Control Specialist to join our fully remote team. This role is essential for ensuring the integrity, safety, and efficacy of pharmaceutical products through rigorous testing and adherence to quality standards. You will be responsible for developing, validating, and implementing analytical test methods for raw materials, in-process samples, and finished products. This involves performing a wide range of analytical techniques, including HPLC, GC, spectroscopy (UV-Vis, IR, AA), and wet chemistry methods. Meticulous documentation of all testing procedures, results, and deviations is paramount, adhering strictly to Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP). You will also participate in the investigation of out-of-specification (OOS) results, identify root causes, and implement corrective and preventive actions (CAPA). Collaboration with formulation scientists, production teams, and regulatory affairs personnel is crucial, requiring strong remote communication skills. The ideal candidate will possess a thorough understanding of pharmacopeial standards (e.g., USP, EP, BP) and regulatory guidelines. This fully remote position offers the flexibility to work from your own location within Kenya, promoting an excellent work-life balance while contributing to a vital industry. You will play a key role in maintaining the quality systems that underpin our client’s commitment to producing high-quality pharmaceuticals. We are seeking a detail-oriented professional with strong analytical acumen and a proactive approach to quality assurance. Your ability to independently manage testing schedules, interpret complex data, and ensure compliance in a virtual environment will be critical. This is an ideal opportunity for a seasoned QC professional looking to apply their expertise in a flexible, remote-working capacity.
Responsibilities:
Responsibilities:
- Perform analytical testing on raw materials, intermediates, and finished pharmaceutical products.
- Develop, validate, and transfer analytical methods.
- Operate and maintain analytical instrumentation (HPLC, GC, Spectrophotometers, etc.).
- Document all testing activities accurately and in compliance with GMP/GLP.
- Investigate out-of-specification (OOS) results and implement CAPA.
- Review and approve batch records and analytical data.
- Ensure compliance with pharmacopeial standards and regulatory requirements.
- Collaborate with cross-functional teams to resolve quality issues.
- Contribute to the continuous improvement of QC processes and systems.
- Maintain laboratory equipment calibration and qualification logs.
- Bachelor's or Master's degree in Chemistry, Pharmacy, or a related life science field.
- Minimum of 6 years of experience in pharmaceutical quality control.
- Extensive hands-on experience with analytical techniques (HPLC, GC, UV-Vis, etc.).
- Strong knowledge of GMP, GLP, and regulatory guidelines.
- Experience with method validation and OOS investigations.
- Excellent attention to detail and accuracy in documentation.
- Strong problem-solving and analytical skills.
- Effective remote communication and interpersonal skills.
- Ability to work independently and manage priorities in a remote setting.
- Must be based in Kenya and available to work within Kenyan business hours.
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Pharmaceutical Quality Control Analyst
Posted 22 days ago
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Job Description
Our client is seeking a meticulous and detail-oriented Pharmaceutical Quality Control Analyst to join their team. This role plays a critical part in ensuring the quality and safety of pharmaceutical products. You will be responsible for conducting a wide range of analytical tests on raw materials, in-process samples, and finished products using various laboratory instruments and methodologies. Accurate documentation and adherence to strict quality standards and regulatory guidelines are paramount.
Key Responsibilities:
Qualifications:
This position offers a hybrid work arrangement, combining essential on-site laboratory work with remote flexibility for data analysis and reporting.
Key Responsibilities:
- Perform routine and non-routine analytical testing of pharmaceutical materials using techniques such as HPLC, GC, UV-Vis, FTIR, and Karl Fischer titration.
- Prepare reagents, solutions, and standards required for testing.
- Document all testing procedures and results accurately and promptly in accordance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
- Analyze and interpret test data, comparing results against established specifications.
- Investigate out-of-specification (OOS) results and deviations, participating in root cause analysis.
- Calibrate and maintain laboratory equipment, ensuring proper functioning and performance.
- Participate in method validation and verification activities.
- Maintain a clean and organized laboratory environment.
- Assist in the preparation of Certificates of Analysis (CoA).
- Stay updated with relevant pharmacopoeial standards (e.g., USP, EP) and regulatory requirements.
Qualifications:
- Bachelor's degree in Chemistry, Pharmacy, Biotechnology, or a related scientific field.
- 1-3 years of experience in a pharmaceutical quality control laboratory setting.
- Hands-on experience with common analytical instruments (HPLC, GC, UV-Vis).
- Knowledge of GMP, GLP, and relevant regulatory guidelines.
- Strong analytical and problem-solving skills.
- Meticulous attention to detail and accuracy in data recording.
- Good written and verbal communication skills.
- Ability to work effectively both independently and as part of a team.
- Proficiency in using laboratory information management systems (LIMS) is a plus.
This position offers a hybrid work arrangement, combining essential on-site laboratory work with remote flexibility for data analysis and reporting.
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4
Lead Pharmaceutical Quality Control Analyst
Posted 22 days ago
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Job Description
Our client is seeking an experienced and detail-oriented Lead Pharmaceutical Quality Control Analyst to manage and execute quality control processes within a fully remote operational framework. This pivotal role ensures that all pharmaceutical products meet stringent regulatory standards and internal quality benchmarks. As the Lead Analyst, you will oversee the performance of analytical testing on raw materials, in-process samples, and finished products using a variety of instrumental and wet chemistry techniques. Your responsibilities will include developing, validating, and implementing QC test methods, troubleshooting analytical issues, and maintaining laboratory equipment in optimal working condition. You will also be responsible for reviewing and approving QC data, ensuring compliance with Good Manufacturing Practices (GMP) and other relevant regulatory guidelines. This position requires a strong understanding of pharmaceutical quality systems, risk assessment, and deviation investigations. The ability to mentor and guide junior QC analysts in a remote setting is essential. Collaboration with R&D, production, and regulatory affairs teams will be a core function, requiring excellent communication and interpersonal skills. You will play a key role in driving continuous improvement initiatives within the quality control department. The ideal candidate will possess a Bachelor's or Master's degree in a relevant scientific discipline, coupled with significant hands-on experience in pharmaceutical quality control. Proficiency in data analysis and reporting, as well as familiarity with pharmacopeial standards (e.g., USP, EP), is required. This is an excellent opportunity to lead quality efforts from a remote position and contribute significantly to patient safety and product integrity. The role is entirely remote, emphasizing robust virtual communication and project management. The location context for this role, though remote, is based out of **Naivasha, Nakuru, KE**.
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5
Remote Pharmaceutical Quality Control Analyst
Posted 22 days ago
Job Viewed
Job Description
Our client, a reputable pharmaceutical company, is seeking a meticulous and highly skilled Remote Pharmaceutical Quality Control Analyst to join their dedicated team. This fully remote position allows you to contribute to ensuring the quality and safety of pharmaceutical products from the convenience of your home office. You will be responsible for conducting various analytical tests, reviewing quality data, and ensuring compliance with stringent regulatory standards. This role requires a strong background in pharmaceutical sciences, analytical chemistry, and quality assurance principles.
Key Responsibilities:
Qualifications:
This role offers a competitive salary and the opportunity to work remotely in a critical function within the pharmaceutical industry. If you are a dedicated professional committed to upholding the highest quality standards, we encourage you to apply.
Key Responsibilities:
- Perform analytical testing of raw materials, in-process samples, and finished pharmaceutical products using established methods and instruments (e.g., HPLC, GC, spectroscopy).
- Review and interpret test results, ensuring they meet predefined specifications and regulatory requirements.
- Document all testing procedures, results, and observations accurately in compliance with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).
- Identify and investigate any deviations from quality standards, troubleshoot analytical issues, and participate in corrective and preventive action (CAPA) investigations.
- Prepare Certificates of Analysis (CoA) and other quality-related documentation.
- Maintain laboratory equipment, ensuring calibration and proper functioning.
- Collaborate with R&D, manufacturing, and regulatory affairs teams to address quality-related inquiries and issues.
- Stay updated on current Good Manufacturing Practices (cGMP), pharmacopeial standards, and relevant regulatory guidelines.
- Participate in internal audits and assist with external regulatory inspections as needed.
- Contribute to the continuous improvement of quality control processes and procedures.
Qualifications:
- Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific discipline.
- Minimum of 3-5 years of experience in pharmaceutical quality control or quality assurance.
- Hands-on experience with analytical instrumentation commonly used in the pharmaceutical industry.
- Proficiency in laboratory techniques and methodologies.
- Strong understanding of cGMP, GLP, and regulatory requirements (e.g., FDA, EMA).
- Excellent attention to detail, accuracy, and organizational skills.
- Strong analytical and problem-solving abilities.
- Effective written and verbal communication skills for documentation and collaboration.
- Ability to work independently and manage time effectively in a remote setting.
- Familiarity with pharmacopeias (e.g., USP, EP) is essential.
This role offers a competitive salary and the opportunity to work remotely in a critical function within the pharmaceutical industry. If you are a dedicated professional committed to upholding the highest quality standards, we encourage you to apply.
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Senior Pharmaceutical Quality Control Analyst
Posted 22 days ago
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Job Description
Our client, a leading force in the pharmaceutical sector, is seeking a highly skilled and meticulous Senior Pharmaceutical Quality Control Analyst to join their dynamic, fully remote team. This pivotal role involves overseeing and executing a wide range of quality control tests and analyses on raw materials, in-process samples, and finished pharmaceutical products. The successful candidate will play a critical part in ensuring that all products meet stringent regulatory standards and internal quality benchmarks. Key responsibilities include developing and validating analytical methods, performing complex laboratory tests using advanced instrumentation (e.g., HPLC, GC, UV-Vis spectrophotometry), troubleshooting analytical issues, and meticulously documenting all findings and results. You will be responsible for interpreting data, preparing comprehensive reports, and contributing to continuous improvement initiatives within the quality control framework. Collaboration with R&D, manufacturing, and regulatory affairs teams will be essential to address any quality concerns and implement corrective actions. This position requires a deep understanding of Good Manufacturing Practices (GMP) and relevant pharmacopeial standards. The ability to work independently, manage multiple priorities effectively, and maintain a high level of accuracy in a remote setting is paramount. This is an excellent opportunity for a seasoned professional looking to make a significant impact from the comfort of their home office in or near Nairobi, Nairobi, KE .
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7
Quality Control Analyst (Pharmaceutical)
Posted 22 days ago
Job Viewed
Job Description
Our client is seeking a meticulous and detail-oriented Quality Control Analyst to join their pharmaceutical division. This role plays a crucial part in ensuring the safety, efficacy, and quality of our pharmaceutical products. The position offers a hybrid work model, combining remote flexibility with essential on-site laboratory work. The successful candidate will be responsible for performing a range of analytical tests and procedures according to established protocols and regulatory standards.
Responsibilities:
Responsibilities:
- Conduct routine and non-routine analytical testing of raw materials, in-process samples, and finished pharmaceutical products using various analytical techniques (e.g., HPLC, GC, UV-Vis Spectroscopy, Titration).
- Prepare reagents, solutions, and standards required for testing.
- Maintain accurate and detailed laboratory records, documenting all procedures, results, and observations in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
- Calibrate and maintain laboratory equipment, ensuring proper functioning and adherence to calibration schedules.
- Investigate out-of-specification (OOS) results, identify root causes, and participate in deviation investigations.
- Assist in the validation and transfer of analytical methods.
- Review and approve testing data and reports.
- Stay informed about current pharmacopeial methods (e.g., USP, BP, EP) and relevant regulatory guidelines.
- Participate in internal and external audits as required.
- Contribute to the continuous improvement of quality control processes and procedures.
- Bachelor's degree in Chemistry, Biochemistry, Pharmacy, or a related scientific field.
- Minimum of 3 years of experience in a pharmaceutical quality control or analytical laboratory setting.
- Proficiency in operating and maintaining analytical instrumentation, particularly HPLC and GC.
- Solid understanding of GMP, GLP, and relevant regulatory requirements.
- Experience with pharmacopeial testing and monographs.
- Strong problem-solving skills and ability to troubleshoot analytical issues.
- Excellent attention to detail and accuracy in data recording and analysis.
- Good organizational and time management skills.
- Effective written and verbal communication abilities.
- Ability to work independently and collaboratively in a hybrid environment, balancing remote tasks with essential on-site laboratory duties.
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8
Remote Pharmaceutical Quality Control Analyst (Trainee)
Posted 15 days ago
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Job Description
Our client, a leading pharmaceutical entity, is seeking a driven and detail-oriented individual for a fully remote Pharmaceutical Quality Control Analyst Trainee position. This is a groundbreaking opportunity to enter the pharmaceutical industry and develop critical skills in quality assurance and control from a remote setting. You will be trained on rigorous testing procedures, data analysis, and regulatory compliance standards that govern pharmaceutical product development and manufacturing. Responsibilities will include reviewing batch records, analyzing laboratory data (virtually), preparing reports on quality testing outcomes, and assisting in the implementation of quality improvement initiatives. The ideal candidate will possess a strong scientific aptitude, meticulous attention to detail, and a solid understanding of basic chemistry and biology principles. Familiarity with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) is advantageous, though not required as comprehensive training will be provided. You must be able to work independently, manage your time effectively in a remote environment, and communicate clearly and concisely with team members and supervisors. This role requires a proactive approach to learning and a commitment to maintaining the highest standards of quality and safety. The successful candidate will gain invaluable experience in a highly regulated industry, contributing to the development of life-saving medications. While the position is fully remote, we are looking for individuals based in or with a strong connection to **Naivasha, Nakuru, KE**, and surrounding regions who are ready to embark on a challenging yet rewarding career path. This is an excellent opportunity for aspiring professionals to gain specialized knowledge and contribute to pharmaceutical excellence from a distance.
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