56 Senior Pharmaceutical Quality Control Analyst jobs in whatjobs
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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Senior Pharmaceutical Quality Control Analyst
Posted 22 days ago
Job Viewed
Job Description
Our client is seeking a highly skilled and meticulous Senior Pharmaceutical Quality Control Analyst to join their dedicated team. This critical role involves ensuring the highest standards of quality and compliance for all pharmaceutical products manufactured and distributed. The successful candidate will possess a deep understanding of analytical techniques, regulatory requirements, and quality management systems within the pharmaceutical industry. This position requires hands-on laboratory work and a commitment to upholding product integrity.
Key Responsibilities:
Qualifications:
This essential role is based on-site in **Nyeri, Nyeri, KE**, contributing directly to the safety and efficacy of pharmaceutical products.
Key Responsibilities:
- Perform a wide range of analytical tests on raw materials, in-process samples, and finished pharmaceutical products using various laboratory instruments and techniques (e.g., HPLC, GC, UV-Vis, titration).
- Analyze test results, interpret data, and document findings accurately in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
- Investigate deviations, out-of-specification (OOS) results, and customer complaints, identifying root causes and implementing corrective and preventive actions (CAPAs).
- Develop, validate, and transfer new analytical methods according to regulatory guidelines.
- Maintain laboratory equipment, ensuring calibration, qualification, and regular performance checks.
- Prepare and review quality control documentation, including test methods, specifications, and standard operating procedures (SOPs).
- Participate in internal and external audits, providing necessary documentation and support.
- Train junior analysts on laboratory procedures, techniques, and safety protocols.
- Stay updated on relevant pharmacopoeial standards (e.g., USP, BP, EP) and regulatory requirements (e.g., FDA, EMA).
- Contribute to the continuous improvement of quality control processes and laboratory operations.
Qualifications:
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biochemistry, or a related life science field.
- Minimum of 5 years of experience in pharmaceutical quality control or analytical testing.
- Proven expertise in operating and maintaining common analytical instruments.
- Thorough understanding of cGMP, GLP, and relevant regulatory guidelines.
- Strong analytical and problem-solving skills with meticulous attention to detail.
- Excellent documentation and report-writing skills.
- Ability to work independently and as part of a team in a laboratory setting.
- Good communication and interpersonal skills.
- Experience with method validation and transfer is highly desirable.
- Knowledge of stability testing protocols.
This essential role is based on-site in **Nyeri, Nyeri, KE**, contributing directly to the safety and efficacy of pharmaceutical products.
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Senior Pharmaceutical Quality Control Analyst
Posted 22 days ago
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Job Description
Our client, a leading pharmaceutical company committed to delivering high-quality medicines, is seeking a dedicated Senior Pharmaceutical Quality Control Analyst. This position is based in **Ruiru, Kiambu, KE**, and offers a hybrid work arrangement, allowing for a blend of remote and in-office responsibilities. The successful candidate will play a critical role in ensuring the quality, safety, and efficacy of our pharmaceutical products through rigorous analytical testing and quality assurance procedures. Your primary responsibilities will include performing a wide range of analytical tests on raw materials, in-process samples, and finished products using sophisticated laboratory equipment such as HPLC, GC, and spectrophotometers. You will be responsible for method development, validation, and transfer, ensuring compliance with all relevant regulatory standards, including GMP and ICH guidelines. This role requires meticulous attention to detail, excellent documentation skills, and the ability to interpret complex analytical data. You will be involved in investigating out-of-specification (OOS) results, identifying root causes, and implementing corrective and preventive actions (CAPAs). The Senior Analyst will also contribute to internal and external audits, ensuring the quality management system is maintained and continuously improved. Collaboration with R&D, production, and regulatory affairs departments is essential to address quality-related issues and support product lifecycle management. The ideal candidate will possess a strong foundation in analytical chemistry, pharmaceutical science, or a related field, coupled with significant hands-on experience in pharmaceutical quality control. Leadership potential and the ability to mentor junior analysts will be highly valued. While this role is hybrid, key laboratory-based activities will require your presence at our Ruiru facility, but strategic planning, data analysis review, and report generation can be effectively managed remotely. This is an excellent opportunity to advance your career in a quality-focused environment within the pharmaceutical industry.
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2
Senior Pharmaceutical Quality Control Analyst
Posted 22 days ago
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Job Description
Our client is seeking a highly skilled and detail-oriented Senior Pharmaceutical Quality Control Analyst to ensure the integrity and compliance of pharmaceutical products. This is a fully remote position, offering an excellent opportunity for a seasoned professional to contribute to pharmaceutical quality assurance from anywhere. You will be responsible for performing a wide range of analytical tests on raw materials, in-process samples, and finished products to verify adherence to strict quality standards and regulatory requirements.
Key responsibilities include operating and maintaining sophisticated laboratory equipment (e.g., HPLC, GC, Spectrophotometers), developing and validating analytical methods, and meticulously documenting all test results and observations. You will collaborate closely with R&D, manufacturing, and regulatory affairs teams to address any quality deviations and support product release. The ideal candidate will possess a strong understanding of Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP), as well as extensive experience with various analytical techniques. Exceptional attention to detail, strong problem-solving skills, and excellent written and verbal communication abilities are crucial for working effectively in a remote laboratory oversight and data review capacity. A commitment to accuracy and compliance is paramount in this role.
Qualifications:
Key responsibilities include operating and maintaining sophisticated laboratory equipment (e.g., HPLC, GC, Spectrophotometers), developing and validating analytical methods, and meticulously documenting all test results and observations. You will collaborate closely with R&D, manufacturing, and regulatory affairs teams to address any quality deviations and support product release. The ideal candidate will possess a strong understanding of Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP), as well as extensive experience with various analytical techniques. Exceptional attention to detail, strong problem-solving skills, and excellent written and verbal communication abilities are crucial for working effectively in a remote laboratory oversight and data review capacity. A commitment to accuracy and compliance is paramount in this role.
Qualifications:
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related science field.
- Minimum of 6 years of experience in pharmaceutical quality control or analytical testing.
- Extensive hands-on experience with analytical instrumentation such as HPLC, GC, UV-Vis spectrophotometry, and titration.
- Proficiency in method development and validation according to regulatory guidelines.
- Solid understanding of GLP and GMP principles.
- Experience with data analysis and interpretation.
- Strong documentation skills and attention to detail.
- Excellent problem-solving and critical thinking abilities.
- Ability to work independently and effectively in a remote environment, managing laboratory oversight and data review.
This advertiser has chosen not to accept applicants from your region.
3
Senior Pharmaceutical Quality Control Analyst
Posted 22 days ago
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Job Description
Our client, a leading pharmaceutical company committed to developing high-quality medicines, is seeking an experienced Senior Pharmaceutical Quality Control Analyst to join their state-of-the-art remote team. This position offers the flexibility to work from anywhere, contributing vital expertise to ensure the efficacy and safety of our client's pharmaceutical products. The ideal candidate will possess a deep understanding of analytical techniques, regulatory compliance, and quality management systems within the pharmaceutical industry. You will be responsible for performing a wide range of analytical tests on raw materials, in-process samples, and finished products, meticulously documenting results and identifying any deviations from quality standards. Your role is critical in upholding the rigorous standards required for drug manufacturing and distribution, ensuring compliance with global regulatory bodies. This is an excellent opportunity for a detail-oriented professional to make a significant impact on public health.
Responsibilities:
Responsibilities:
- Perform complex analytical testing on pharmaceutical raw materials, intermediates, and finished products using various techniques such as HPLC, GC, UV-Vis spectrophotometry, and Karl Fischer titration for projects supporting operations related to **Mombasa, Mombasa, KE** and international markets.
- Develop, validate, and transfer analytical methods according to ICH guidelines and regulatory requirements.
- Analyze and interpret test results, compare them against established specifications, and prepare detailed reports on findings.
- Investigate Out-of-Specification (OOS) and Out-of-Trend (OOT) results, identify root causes, and recommend corrective and preventive actions (CAPAs).
- Maintain and calibrate laboratory equipment, ensuring its optimal performance and compliance with regulatory standards.
- Ensure adherence to Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant quality systems and regulatory guidelines.
- Review and approve analytical data, method validation reports, and other quality-related documentation.
- Collaborate with R&D, manufacturing, and regulatory affairs departments to support product development and lifecycle management.
- Train and mentor junior quality control analysts, providing guidance on analytical techniques and laboratory procedures.
- Contribute to the continuous improvement of quality control processes and laboratory operations.
- Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, Biochemistry, or a related life science discipline.
- Minimum of 6 years of hands-on experience in pharmaceutical quality control or analytical development.
- Proficiency in operating and maintaining analytical instrumentation commonly used in pharmaceutical QC (e.g., HPLC, GC, dissolution testers).
- Solid understanding of ICH guidelines, GMP, and other relevant pharmaceutical regulatory requirements.
- Experience with method development and validation is essential.
- Strong analytical and problem-solving skills with meticulous attention to detail.
- Excellent written and verbal communication skills, with the ability to clearly document scientific data and findings.
- Proven ability to work independently and manage time effectively in a remote laboratory support role.
- Experience with LIMS (Laboratory Information Management System) is a plus.
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4
Senior Pharmaceutical Quality Control Analyst
Posted 22 days ago
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Job Description
Our client is seeking a highly motivated and experienced Senior Pharmaceutical Quality Control Analyst to join their dynamic, fully remote team. In this critical role, you will be responsible for ensuring the quality and integrity of pharmaceutical products through rigorous testing and analysis. You will conduct in-process and finished product testing, validate analytical methods, and maintain accurate and detailed records of all testing performed. This position demands a meticulous approach to work, adherence to strict regulatory guidelines (GMP, ICH), and the ability to interpret complex scientific data. You will also be involved in troubleshooting laboratory equipment, participating in deviation investigations, and contributing to the continuous improvement of quality control processes. The ideal candidate will possess strong knowledge of various analytical techniques such as HPLC, GC, UV-Vis spectroscopy, and dissolution testing. Collaboration with cross-functional teams, including R&D, Manufacturing, and Regulatory Affairs, will be essential to address quality issues and implement corrective actions. This is a remote-first position, requiring excellent communication and organizational skills to thrive in a virtual environment. You will need to be self-driven, proactive, and capable of managing your workload efficiently without direct supervision. The ability to work independently and as part of a globally distributed team is paramount. The role involves reviewing and approving raw data, ensuring compliance with all relevant pharmacopeial standards, and contributing to the development and validation of new testing procedures. This opportunity offers the chance to make a significant impact on the quality of life-saving medications. We are looking for individuals passionate about science, dedicated to excellence, and committed to upholding the highest standards of pharmaceutical quality. The physical location for this role, as per company policy, is associated with Embu, Embu, KE , but the work is performed entirely remotely.
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5
Senior Pharmaceutical Quality Control Analyst
Posted 22 days ago
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Job Description
Our client is seeking a highly diligent and experienced Senior Pharmaceutical Quality Control Analyst to join their fully remote team. This critical role ensures the highest standards of quality and compliance for 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 sophisticated laboratory instruments. The ideal candidate will possess a strong understanding of Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and relevant pharmacopeial standards (e.g., USP, EP). Key responsibilities include method development and validation, stability testing, and maintaining detailed and accurate laboratory records. You will also be involved in investigating deviations, out-of-specification results, and implementing corrective and preventive actions (CAPAs). Proficiency with analytical instrumentation such as HPLC, GC, UV-Vis, FTIR, and dissolution apparatus is essential. As a senior member of the team, you will provide guidance and training to junior analysts, review analytical data, and contribute to quality assurance initiatives. This remote position requires exceptional attention to detail, strong problem-solving abilities, and excellent written and verbal communication skills. The ability to work independently, manage time effectively, and collaborate with cross-functional teams in a virtual environment is crucial. Our client is committed to producing safe and effective medicines, and this role is integral to that mission. A Bachelor's or Master's degree in Pharmaceutical Sciences, Chemistry, or a related life science discipline is required, along with a minimum of 5 years of relevant experience in pharmaceutical quality control. Experience with regulatory inspections and a thorough understanding of quality management systems are highly desirable. If you are a detail-oriented quality professional seeking a challenging and rewarding remote opportunity within the pharmaceutical industry, we encourage you to apply. This position offers competitive remuneration and the flexibility of a work-from-home arrangement.
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6
Senior Pharmaceutical Quality Control Analyst
Posted 22 days ago
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Job Description
Our client, a leading pharmaceutical company, is seeking a meticulous Senior Pharmaceutical Quality Control Analyst to join their team. This role involves ensuring the highest standards of quality and compliance for all manufactured pharmaceutical products. You will perform a variety of laboratory tests on raw materials, in-process samples, and finished products using advanced analytical techniques and instrumentation, such as HPLC, GC, and spectroscopy. Responsibilities include accurate data recording, thorough investigation of out-of-specification (OOS) results, and contribution to method validation and development. The Senior Analyst will also play a key role in maintaining and calibrating laboratory equipment, ensuring adherence to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). You will be expected to review and approve analytical data, prepare reports, and participate in internal and external audits. A strong understanding of pharmacopoeial standards (e.g., USP, BP, EP) and regulatory guidelines (e.g., FDA, EMA) is essential. This position requires a Bachelor's or Master's degree in Pharmacy, Chemistry, or a related scientific field, coupled with significant experience in pharmaceutical QC. The ability to work effectively both independently and as part of a collaborative team, while managing multiple tasks and prioritizing effectively, is crucial. This role offers a hybrid work arrangement, providing a balance between on-site laboratory work and remote data analysis or report writing. If you are dedicated to ensuring drug safety and efficacy through rigorous quality control, and possess excellent analytical and problem-solving skills, we invite you to apply and contribute to our mission of delivering high-quality medicines.
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7
Senior Pharmaceutical Quality Control Analyst
Posted 20 days ago
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Job Description
**Our client**, a leading pharmaceutical company, is seeking a highly experienced Senior Pharmaceutical Quality Control Analyst to join their remote team. This position plays a vital role in ensuring the quality, safety, and efficacy of pharmaceutical products. You will be responsible for designing, implementing, and validating analytical methods, performing routine testing of raw materials, in-process samples, and finished products, and interpreting results according to established specifications and regulatory guidelines. Key responsibilities include operating and maintaining sophisticated analytical instrumentation (e.g., HPLC, GC, UV-Vis spectrophotometry), troubleshooting analytical issues, and maintaining accurate and comprehensive laboratory records. You will also contribute to the development of quality control procedures, participate in regulatory inspections, and collaborate with cross-functional teams, including R&D, manufacturing, and regulatory affairs. The ideal candidate will have a strong scientific background, with a Bachelor's or Master's degree in Chemistry, Pharmacy, or a related life science field, coupled with extensive experience in pharmaceutical quality control. A thorough understanding of cGMP, ICH guidelines, and pharmacopoeial standards (e.g., USP, EP) is essential. Excellent analytical, problem-solving, and documentation skills are required. This is a fully remote position, requiring excellent self-management, communication, and the ability to work independently while contributing to team objectives. You must be meticulous, detail-oriented, and committed to upholding the highest standards of quality in pharmaceutical manufacturing. This is an exceptional opportunity to leverage your expertise in a critical role that directly impacts patient health.
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8
Senior Pharmaceutical Quality Control Analyst
Posted 20 days ago
Job Viewed
Job Description
Our client is seeking a highly motivated and experienced Senior Pharmaceutical Quality Control Analyst to join their dynamic remote team. This role is crucial in ensuring the consistent quality and safety of pharmaceutical products by meticulously performing a variety of laboratory tests and analytical procedures. You will be responsible for the accurate and timely execution of tests on raw materials, in-process samples, and finished products according to established protocols and regulatory standards. This includes operating and maintaining sophisticated analytical instruments such as HPLC, GC, UV-Vis spectrophotometers, and dissolution testers. Your expertise will be vital in interpreting complex data, troubleshooting analytical issues, and contributing to method validation and development. This is a fully remote position, allowing you to contribute your skills from the comfort of your home office, based in the region of Mlolongo, Machakos, KE . The ideal candidate will possess a strong understanding of Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP). You will also play a key role in documenting all testing activities, maintaining accurate records, and preparing comprehensive reports for regulatory submissions and internal reviews. Collaboration with cross-functional teams, including R&D, production, and regulatory affairs, will be essential to address quality concerns and implement corrective actions. This position demands exceptional attention to detail, problem-solving abilities, and a commitment to upholding the highest standards of pharmaceutical quality. Your work will directly impact patient safety and the integrity of our client's product portfolio. We are looking for an individual who is proactive, detail-oriented, and can work independently with minimal supervision while also contributing effectively to a team environment. Proficiency in data analysis software and laboratory information management systems (LIMS) is highly desirable. The ability to adapt to evolving regulatory landscapes and technological advancements in pharmaceutical analysis is also a significant advantage.
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