7,997 Senior Pharmaceutical Quality Control Scientist jobs in Kenya
Lead Pharmaceutical Quality Control Scientist
Posted 9 days ago
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Job Description
Our client, a prominent pharmaceutical firm, is searching for a seasoned Lead Pharmaceutical Quality Control Scientist to spearhead their remote quality assurance operations. This role demands a meticulous and experienced professional dedicated to upholding the highest standards of pharmaceutical quality and compliance. You will be responsible for overseeing all aspects of quality control testing, method validation, and stability studies for a diverse range of pharmaceutical products. This includes developing and implementing robust quality control procedures, ensuring adherence to Good Manufacturing Practices (GMP) and other regulatory requirements. The Lead Scientist will manage a team of quality control analysts, providing technical guidance, training, and performance management. Your expertise will be crucial in troubleshooting analytical issues, investigating deviations, and implementing corrective and preventive actions (CAPA). You will also be involved in the review and approval of batch records, analytical reports, and quality agreements. A significant part of this role involves collaborating with R&D, manufacturing, and regulatory affairs departments to ensure seamless product development and lifecycle management. This is a remote position, offering the flexibility to work from anywhere while making a critical contribution to public health. The successful candidate will possess a deep understanding of analytical techniques, instrumentation (e.g., HPLC, GC, MS), and pharmacopeial standards. Experience in pharmaceutical formulation and process development is highly desirable. You should demonstrate excellent leadership, communication, and problem-solving skills. Your commitment to quality and patient safety will be paramount. We are looking for individuals who are passionate about advancing pharmaceutical science and who can thrive in a virtual, collaborative environment. The ability to interpret complex data and translate it into actionable insights is essential.Naivasha, Nakuru, KE is the designated regional hub, but the role is fully remote.
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Principal Pharmaceutical Quality Control Scientist
Posted 22 days ago
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Job Description
WhatJobs is seeking a highly experienced and detail-oriented Principal Pharmaceutical Quality Control Scientist to join our esteemed R&D team. This is a critical, fully remote role focused on ensuring the highest standards of quality and compliance in pharmaceutical product development and manufacturing. The successful candidate will play a pivotal role in establishing, implementing, and maintaining robust quality control systems and processes. You will be responsible for overseeing analytical testing, method validation, stability studies, and ensuring adherence to global regulatory standards, including GMP (Good Manufacturing Practices). This position requires a deep understanding of pharmaceutical sciences, analytical chemistry, and regulatory affairs.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Develop, validate, and implement analytical methods for raw materials, in-process samples, and finished pharmaceutical products using techniques such as HPLC, GC, UV-Vis, FTIR, and dissolution testing.
- Oversee and conduct stability studies according to ICH guidelines to assess product shelf-life and storage conditions.
- Review and approve batch records, analytical data, and quality control reports to ensure product quality and regulatory compliance.
- Investigate deviations, out-of-specification (OOS) results, and out-of-trend (OOT) data, determining root causes and implementing corrective and preventive actions (CAPAs).
- Contribute to the design and execution of validation protocols for analytical methods and equipment.
- Ensure that all quality control activities comply with cGMP, FDA, and other relevant regulatory agency requirements.
- Train and mentor junior QC scientists and technicians, providing technical guidance and support.
- Collaborate with R&D, manufacturing, and regulatory affairs departments to resolve quality issues and support product lifecycle management.
- Maintain laboratory equipment, ensuring proper calibration, maintenance, and documentation.
- Stay abreast of new scientific advancements, regulatory changes, and industry best practices in pharmaceutical quality control.
Qualifications:
- Master's or Ph.D. in Pharmaceutical Sciences, Chemistry, Analytical Chemistry, or a related field.
- A minimum of 10 years of experience in pharmaceutical quality control, with at least 3 years in a lead or principal scientist role.
- Extensive hands-on experience with a variety of analytical techniques relevant to pharmaceutical quality control.
- Strong knowledge of cGMP regulations, ICH guidelines, and pharmacopeial standards (USP, EP).
- Proven experience in method validation, OOS investigations, and CAPA management.
- Excellent analytical, problem-solving, and critical thinking skills.
- Strong leadership, communication, and interpersonal skills, with the ability to effectively manage remote teams and projects.
- Proficiency in laboratory information management systems (LIMS) and other relevant software.
- Detail-oriented with a commitment to accuracy and quality.
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Senior Pharmaceutical Quality Control Scientist
Posted 13 days ago
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Job Description
Our client, a leading pharmaceutical innovator, is seeking a highly qualified Senior Pharmaceutical Quality Control Scientist to join their dedicated team. This is a fully remote position, offering a unique opportunity to contribute to ensuring the quality and safety of pharmaceutical products from anywhere. You will be responsible for developing, validating, and executing analytical methods to assess the quality of raw materials, in-process samples, and finished drug products. This role requires meticulous attention to detail, a strong understanding of pharmaceutical regulations, and advanced analytical chemistry skills.
Key responsibilities include:
The ideal candidate will possess a Master's or Ph.D. in Pharmaceutical Sciences, Chemistry, Analytical Chemistry, or a related field, with a minimum of 5 years of experience in pharmaceutical quality control. Extensive hands-on experience with analytical instrumentation (HPLC, GC, spectroscopy) and method validation is essential. A thorough understanding of Good Manufacturing Practices (GMP), ICH guidelines, and other relevant regulatory requirements is mandatory. Excellent analytical, problem-solving, and documentation skills are critical. Strong communication and interpersonal skills are necessary for effective remote collaboration with cross-functional teams. You will be remotely contributing to ensuring the highest standards of quality for our pharmaceutical products, supporting operations that may involve **Machakos, Machakos, KE**. This is an exceptional opportunity to make a significant impact in ensuring drug safety and efficacy. We are looking for a detail-oriented scientist with a passion for quality and a commitment to excellence in pharmaceutical manufacturing.
Key responsibilities include:
- Developing, validating, and implementing analytical methods for raw materials, intermediates, and finished pharmaceutical products using techniques such as HPLC, GC, UV-Vis, and dissolution testing.
- Performing routine quality control testing according to established protocols and regulatory guidelines (e.g., GMP, ICH).
- Investigating and troubleshooting Out-of-Specification (OOS) results and deviations, providing detailed root cause analysis.
- Maintaining laboratory equipment, ensuring proper calibration, and adhering to all safety procedures.
- Reviewing and approving analytical data, batch records, and method validation reports.
- Participating in regulatory inspections and audits, ensuring compliance with all relevant standards.
- Collaborating with R&D, manufacturing, and regulatory affairs departments to resolve quality-related issues.
- Staying current with the latest advancements in pharmaceutical analysis and quality control.
- Contributing to the continuous improvement of quality systems and processes.
- Training and mentoring junior QC analysts on analytical techniques and procedures.
The ideal candidate will possess a Master's or Ph.D. in Pharmaceutical Sciences, Chemistry, Analytical Chemistry, or a related field, with a minimum of 5 years of experience in pharmaceutical quality control. Extensive hands-on experience with analytical instrumentation (HPLC, GC, spectroscopy) and method validation is essential. A thorough understanding of Good Manufacturing Practices (GMP), ICH guidelines, and other relevant regulatory requirements is mandatory. Excellent analytical, problem-solving, and documentation skills are critical. Strong communication and interpersonal skills are necessary for effective remote collaboration with cross-functional teams. You will be remotely contributing to ensuring the highest standards of quality for our pharmaceutical products, supporting operations that may involve **Machakos, Machakos, KE**. This is an exceptional opportunity to make a significant impact in ensuring drug safety and efficacy. We are looking for a detail-oriented scientist with a passion for quality and a commitment to excellence in pharmaceutical manufacturing.
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Remote Pharmaceutical Quality Control Scientist
Posted 12 days ago
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Job Description
Our client, a rapidly growing pharmaceutical company, is seeking a dedicated and meticulous Remote Pharmaceutical Quality Control Scientist to enhance their global quality assurance team. This position focuses on ensuring that all pharmaceutical products meet stringent regulatory standards and internal quality benchmarks, all coordinated and executed from a remote work setup. The role involves reviewing and analyzing quality control data, developing and validating analytical methods, and contributing to the continuous improvement of quality systems. You will be responsible for performing comprehensive data integrity checks, identifying deviations, and initiating investigations for any out-of-specification results. Strong knowledge of Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and relevant pharmacopoeial standards (e.g., USP, EP) is essential. The successful candidate will possess excellent analytical skills, a strong understanding of statistical process control, and experience with various analytical techniques (e.g., HPLC, GC, spectroscopy). As a remote scientist, you must be highly organized, self-motivated, and capable of managing complex projects independently. Effective written and verbal communication skills are crucial for collaborating with internal teams, external partners, and regulatory bodies. This role offers a unique opportunity to contribute to patient safety and product efficacy without the need for on-site presence. You will play a vital part in ensuring the compliance and quality of our client's pharmaceutical products. The ability to interpret regulatory guidelines and apply them to real-world quality control scenarios is a key requirement. You will also be involved in the preparation of documentation for regulatory submissions and audits. This position demands a high level of scientific rigor and a commitment to maintaining the highest ethical standards in pharmaceutical quality. Your expertise will directly influence the release of safe and effective medications to the market.
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Senior Pharmaceutical Quality Control Scientist - Remote
Posted 21 days ago
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Job Description
Our client, a leading pharmaceutical research and development company, is seeking a highly experienced Senior Pharmaceutical Quality Control Scientist to join their fully remote R&D team. This vital role will involve overseeing and executing rigorous quality control testing for pharmaceutical products, ensuring compliance with stringent regulatory standards (e.g., FDA, EMA) and company policies. You will be responsible for method development and validation, data analysis, stability studies, and troubleshooting analytical issues. The ideal candidate will possess a deep understanding of analytical chemistry techniques, pharmaceutical manufacturing processes, and quality assurance principles, along with excellent problem-solving and documentation skills. This is a significant opportunity to contribute to the development of life-saving medicines from a remote setting, ensuring the safety and efficacy of pharmaceutical products globally. Your scientific expertise and commitment to quality will be crucial.
Key Responsibilities:
Key Responsibilities:
- Develop, validate, and implement analytical methods for raw materials, in-process samples, and finished pharmaceutical products using techniques such as HPLC, GC, UV-Vis, FTIR, and mass spectrometry.
- Perform routine quality control testing according to established protocols and Standard Operating Procedures (SOPs).
- Analyze and interpret complex analytical data, generating accurate and comprehensive reports.
- Investigate out-of-specification (OOS) results and deviations, identifying root causes and implementing corrective and preventive actions (CAPAs).
- Conduct stability studies to determine product shelf-life and storage conditions.
- Maintain and calibrate laboratory equipment, ensuring optimal performance and compliance with GLP/GMP guidelines.
- Review and approve analytical data, batch records, and validation reports.
- Contribute to the development and continuous improvement of quality control processes and procedures.
- Stay current with scientific advancements, regulatory guidelines, and industry best practices in pharmaceutical quality control.
- Provide technical expertise and mentorship to junior QC scientists.
- Collaborate with R&D, manufacturing, and regulatory affairs teams to support product development and lifecycle management.
- Prepare and present findings for internal reviews and regulatory submissions.
- Ph.D. or Master's degree in Analytical Chemistry, Pharmaceutical Sciences, Chemistry, or a related field.
- Minimum of 7 years of experience in pharmaceutical quality control, analytical development, or a related laboratory setting.
- Extensive hands-on experience with various analytical instrumentation (HPLC, GC, MS, etc.) and data analysis software.
- Strong understanding of Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and relevant regulatory guidelines (FDA, EMA).
- Proven ability in method development and validation for pharmaceutical products.
- Excellent data interpretation, troubleshooting, and problem-solving skills.
- Strong written and verbal communication skills, essential for remote documentation and collaboration.
- Meticulous attention to detail and a commitment to scientific accuracy.
- Ability to work independently and manage multiple projects in a remote environment.
- Experience with laboratory information management systems (LIMS) is a plus.
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4
Pharmaceutical Quality Control Specialist
Posted 14 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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5
Remote Pharmaceutical Quality Control Specialist
Posted 23 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 16 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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7
Remote Senior Pharmaceutical Quality Control Specialist
Posted 23 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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8
Lead Pharmaceutical Formulation Scientist (Pharmaceutical)
Posted 15 days ago
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Job Description
Our client is actively recruiting a highly accomplished Lead Pharmaceutical Formulation Scientist for a fully remote, full-time position. This role is central to the innovation and development of novel pharmaceutical products, from concept through to clinical trials and commercialization. The ideal candidate will possess an advanced degree (M.Sc. or Ph.D.) in Pharmaceutical Sciences, Chemistry, or a related field, coupled with extensive experience in drug formulation, pre-formulation studies, and dosage form design. You will lead the formulation development of new chemical entities (NCEs) and the improvement of existing drug products, ensuring optimal bioavailability, stability, and patient compliance. Key responsibilities include designing and executing experimental plans for solid dosage forms, sterile injectables, or other relevant dosage types, as well as troubleshooting formulation challenges. You will interpret complex analytical data, conduct characterization studies, and ensure all activities comply with regulatory guidelines (e.g., GMP, ICH). This role involves close collaboration with analytical development, regulatory affairs, and manufacturing teams. The successful applicant will have a strong understanding of physical chemistry, material science, and their application in pharmaceutical development. Excellent project management, leadership, and communication skills are essential, enabling effective collaboration in a remote setting. If you are passionate about advancing drug development and have a proven ability to drive formulation projects from bench to clinic, we invite you to apply. This remote position allows you to contribute your expertise to our client's mission, supporting their drug discovery and development efforts potentially impacting areas around Machakos, Machakos, KE .
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