8 Pharmaceutical Quality Control Analyst jobs in whatjobs
Pharmaceutical Quality Control Analyst
Posted 5 days ago
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Job Description
Our client, a leading pharmaceutical company, is looking for a meticulous and experienced Pharmaceutical Quality Control Analyst to join their team. This role requires a blend of remote work and on-site presence, ensuring flexibility while maintaining critical laboratory operations. You will be responsible for performing a range of analytical tests on raw materials, in-process samples, and finished pharmaceutical products to ensure they meet stringent quality standards and regulatory requirements. Your duties will include operating and maintaining laboratory equipment, developing and validating analytical methods, documenting test results accurately, and investigating any deviations or out-of-specification results. The ideal candidate will possess a Bachelor's degree in Pharmacy, Chemistry, or a related scientific discipline, with proven experience in pharmaceutical quality control. Strong knowledge of GMP (Good Manufacturing Practices) and relevant analytical techniques (e.g., HPLC, GC, spectroscopy) is essential. Excellent analytical, problem-solving, and documentation skills are paramount. You must be highly organized, detail-oriented, and capable of working effectively both independently and as part of a collaborative team in a hybrid work model. This role offers a fantastic opportunity to contribute to the quality and safety of pharmaceutical products, supporting operations in the **Garissa, Garissa, KE** area.
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Pharmaceutical Quality Control Analyst
Posted 13 days ago
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Job Description
Our client, a rapidly growing pharmaceutical company, is looking for an experienced Pharmaceutical Quality Control Analyst to join their team in Garissa, Garissa, KE . This role is critical in ensuring the quality, safety, and efficacy of all manufactured pharmaceutical products. The successful candidate will perform a wide range of analytical tests on raw materials, in-process samples, and finished products using various laboratory techniques and equipment. Responsibilities include executing method validation protocols, maintaining accurate and detailed laboratory records, and adhering strictly to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). You will be expected to troubleshoot analytical methods, investigate out-of-specification (OOS) results, and collaborate with production and formulation teams to resolve quality issues. The analyst will also be involved in the stability testing programs, ensuring product shelf-life compliance. Proficiency in using analytical instrumentation such as HPLC, GC, UV-Vis spectrophotometers, and dissolution testers is essential. The ideal candidate will hold a Bachelor's degree in Pharmacy, Chemistry, Biochemistry, or a related life science discipline, coupled with a minimum of 3 years of hands-on experience in pharmaceutical quality control. A thorough understanding of pharmacopoeial standards (e.g., BP, USP, EP) and regulatory requirements within the pharmaceutical industry is mandatory. Excellent attention to detail, strong analytical and problem-solving abilities, and the capacity to work effectively under pressure are key attributes. The ability to work independently and as part of a collaborative team is also important. This position offers a competitive salary and benefits package, along with opportunities for professional growth within a reputable organization committed to advancing healthcare solutions. If you are a meticulous scientist dedicated to upholding the highest quality standards in pharmaceuticals, we invite you to submit your application.
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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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Pharmaceutical Quality Control Analyst
Posted 22 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is seeking a meticulous and detail-oriented Pharmaceutical Quality Control Analyst to join their team. This role is crucial in ensuring the quality, safety, and efficacy of pharmaceutical products manufactured by our client. The successful candidate will be responsible for performing a wide range of analytical tests on raw materials, in-process samples, and finished products using various laboratory instruments and techniques. This includes, but is not limited to, High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), UV-Vis Spectrophotometry, and titration methods. You will meticulously document all test results, prepare Certificates of Analysis (CoAs), and maintain accurate laboratory records in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). Furthermore, you will be involved in method validation and transfer activities, ensuring that analytical procedures are robust and reliable. Identifying and investigating out-of-specification (OOS) results, deviations, and customer complaints will be a key responsibility, requiring strong problem-solving skills and a thorough understanding of pharmaceutical quality systems. You will also participate in internal and external audits and contribute to the continuous improvement of quality control processes. The ideal candidate will possess a Bachelor's or Master's degree in Chemistry, Pharmacy, or a related scientific field, coupled with significant hands-on experience in a pharmaceutical QC laboratory setting. Strong knowledge of analytical chemistry principles, instrumentation, and regulatory guidelines (e.g., FDA, EMA) is essential. Excellent written and verbal communication skills, along with strong organizational and time-management abilities, are required. This role offers a hybrid work arrangement, balancing essential on-site laboratory work with remote administrative and data analysis tasks. You will be expected to work collaboratively with R&D, manufacturing, and regulatory affairs teams to ensure product quality throughout the lifecycle. This position is based in **Ongata Rongai, Kajiado, KE**, and involves a combination of on-site and remote responsibilities.
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Pharmaceutical Quality Control Analyst
Posted 22 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is seeking a meticulous and experienced Pharmaceutical Quality Control Analyst to join their manufacturing facility. This position requires dedicated on-site presence to ensure the highest standards of quality in our pharmaceutical products. The successful candidate will be responsible for conducting a wide range of laboratory tests and analyses to ensure raw materials, in-process samples, and finished products meet stringent quality specifications and regulatory requirements. This role demands a strong understanding of analytical chemistry, Good Manufacturing Practices (GMP), and quality assurance principles within the pharmaceutical industry. The ideal candidate will possess excellent attention to detail, a systematic approach to work, and the ability to perform complex analytical procedures accurately and efficiently.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Perform analytical testing on raw materials, intermediates, finished products, and packaging materials using various laboratory techniques (e.g., HPLC, GC, UV-Vis Spectroscopy, Titration).
- Ensure all testing is conducted in compliance with established Standard Operating Procedures (SOPs), GMP, and relevant regulatory guidelines (e.g., FDA, EMA).
- Prepare reagents, standards, and samples for analytical testing.
- Calibrate and maintain laboratory equipment, ensuring it is in proper working order and records are meticulously kept.
- Document all test results, observations, and deviations accurately and in a timely manner in laboratory notebooks and electronic systems.
- Investigate out-of-specification (OOS) results and deviations, identifying root causes and recommending corrective and preventive actions (CAPAs).
- Participate in method validation and verification activities as required.
- Contribute to the review and improvement of SOPs and quality control procedures.
- Collaborate with other departments, such as Production, R&D, and Quality Assurance, to resolve quality-related issues.
- Maintain a clean and safe laboratory environment.
Qualifications:
- A Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science discipline.
- Minimum of 3-5 years of experience in a Pharmaceutical Quality Control laboratory setting.
- Hands-on experience with analytical instrumentation commonly used in pharmaceutical QC (e.g., HPLC, GC, FTIR, UV-Vis, dissolution apparatus).
- Solid understanding of GMP, GLP, and pharmaceutical quality systems.
- Proficiency in performing analytical method validation and OOS investigations.
- Excellent laboratory technique, attention to detail, and data integrity.
- Strong documentation skills and the ability to maintain accurate records.
- Good problem-solving and critical-thinking abilities.
- Ability to work independently and as part of a team.
- Familiarity with relevant pharmacopeias (e.g., USP, EP, BP) is a plus.
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Pharmaceutical Quality Control Analyst
Posted 21 days ago
Job Viewed
Job Description
Our client is seeking a meticulous and dedicated Pharmaceutical Quality Control Analyst to join their team in a fully remote capacity. This role is vital in ensuring the quality and safety of pharmaceutical products through rigorous testing and analysis. You will be responsible for performing a wide range of analytical tests on raw materials, in-process samples, and finished products according to established protocols and regulatory guidelines. This includes utilizing various laboratory techniques and instrumentation such as HPLC, GC, UV-Vis spectroscopy, and titration. You will meticulously document all testing procedures, results, and deviations in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). The role involves reviewing and approving analytical data, preparing Certificates of Analysis (CoAs), and troubleshooting analytical methods when necessary. You will also participate in method validation and transfer activities, and contribute to the investigation of out-of-specification (OOS) results. Maintaining laboratory equipment, ensuring proper calibration, and managing laboratory supplies will be part of your responsibilities. The ideal candidate will possess a Bachelor's or Master's degree in Pharmacy, Chemistry, Biochemistry, or a related life science field. A minimum of 3 years of experience in pharmaceutical quality control or quality assurance is required. Hands-on experience with analytical instrumentation and adherence to regulatory standards (e.g., ICH, FDA) are essential. Strong attention to detail, excellent organizational skills, and proficiency in data analysis and scientific documentation are paramount. As this is a remote role, you must be self-motivated, disciplined, and capable of managing your workload effectively without direct supervision. Excellent written and verbal communication skills are necessary for reporting and collaborating with team members. Join our forward-thinking pharmaceutical company and contribute to delivering high-quality medicines.
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5
Pharmaceutical Quality Control Analyst
Posted 19 days ago
Job Viewed
Job Description
Our client is seeking a meticulous and analytical Pharmaceutical Quality Control Analyst to join their team. This role offers a Hybrid work model, combining remote flexibility with essential on-site laboratory work. The ideal candidate will possess a strong background in pharmaceutical sciences, analytical chemistry, and quality assurance principles. You will be responsible for performing a wide range of laboratory tests on raw materials, in-process samples, and finished pharmaceutical products to ensure they meet stringent quality standards and regulatory requirements. This includes utilizing various analytical techniques and instrumentation such as HPLC, GC, spectroscopy, and wet chemistry methods. Key responsibilities involve the accurate execution of test methods, meticulous documentation of results, investigation of out-of-specification (OOS) results, and contribution to method validation activities. The Pharmaceutical Quality Control Analyst will play a vital role in upholding the integrity and safety of pharmaceutical products throughout their lifecycle. Strong attention to detail, excellent record-keeping skills, and a thorough understanding of Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) are essential for success in this role. The ability to collaborate effectively with cross-functional teams, both remotely and on-site, is also crucial.
Key Responsibilities:
Key Responsibilities:
- Perform analytical testing on raw materials, intermediate products, and finished pharmaceutical goods using various laboratory techniques and equipment.
- Conduct tests for identity, purity, strength, and quality according to established specifications and standard operating procedures (SOPs).
- Operate and maintain analytical instruments such as HPLC, GC, UV-Vis spectrophotometers, and dissolution apparatus.
- Accurately record and document all testing results, observations, and deviations in laboratory notebooks and LIMS.
- Investigate and troubleshoot out-of-specification (OOS) or out-of-trend (OOT) results, participating in root cause analysis.
- Assist in the validation and qualification of analytical methods and equipment.
- Ensure compliance with all relevant regulatory guidelines, including GMP, GLP, and ICH.
- Prepare and review quality control documentation, including test reports and certificates of analysis.
- Participate in internal and external audits as required.
- Collaborate with R&D, Production, and Regulatory Affairs departments to address quality-related issues.
- Maintain a safe and organized laboratory environment.
- Contribute to continuous improvement initiatives within the quality control department.
- Bachelor's degree in Chemistry, Pharmaceutical Sciences, Biochemistry, or a related scientific discipline.
- Minimum of 3-5 years of experience in pharmaceutical quality control or analytical laboratory setting.
- Hands-on experience with HPLC, GC, and other common analytical instrumentation.
- Thorough understanding of pharmaceutical quality systems, GMP, and GLP.
- Proficiency in data analysis and interpretation.
- Excellent laboratory notebook keeping and documentation skills.
- Strong problem-solving abilities and attention to detail.
- Good written and verbal communication skills.
- Ability to work effectively both independently and as part of a hybrid team.
- Familiarity with pharmacopoeias (e.g., USP, EP, BP) is advantageous.
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Pharmaceutical Quality Control Analyst
Posted 4 days ago
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Job Description
Our client, a prestigious pharmaceutical company dedicated to advancing healthcare, is seeking a meticulous and detail-oriented Pharmaceutical Quality Control Analyst. This hybrid role offers a dynamic blend of remote work flexibility and essential on-site laboratory presence, ensuring rigorous quality standards for our client's innovative drug formulations. You will be responsible for conducting a wide range of analytical tests on raw materials, in-process samples, and finished pharmaceutical products. Your key duties will include operating sophisticated laboratory equipment (e.g., HPLC, GC, UV-Vis spectrophotometers), performing method validation, documenting all testing procedures and results accurately, and adhering strictly to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). We are looking for candidates with a strong scientific background, ideally with a degree in Pharmacy, Chemistry, Biotechnology, or a related life science discipline. Previous experience in a pharmaceutical QC laboratory setting is highly desirable. A thorough understanding of analytical techniques, regulatory requirements (e.g., FDA, EMA), and quality management systems is essential. Excellent record-keeping skills, a proactive approach to problem-solving, and the ability to work independently as well as collaboratively within a team are crucial. This position offers a significant opportunity to contribute to the safety and efficacy of vital medicines, working within a state-of-the-art facility. The hybrid model ensures you can leverage remote capabilities for documentation and analysis while performing critical hands-on laboratory work. If you are a dedicated scientist passionate about pharmaceutical quality and seeking a role that combines advanced technical work with flexible arrangements, we encourage you to apply for this opportunity in Kakamega, Kakamega, KE .
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