19 Senior Pharmaceutical Quality Control Analyst Remote jobs in whatjobs
Senior Pharmaceutical Quality Control Analyst - Remote
Posted 20 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company dedicated to advancing healthcare, is seeking a highly experienced Senior Pharmaceutical Quality Control Analyst to join their esteemed team. This pivotal role will operate on a fully remote basis, ensuring the integrity and compliance of our pharmaceutical products. You will be responsible for executing a wide range of analytical tests, interpreting results, and maintaining meticulous documentation according to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). Key duties include performing assays, stability testing, impurity profiling, and method validation using various sophisticated analytical instruments such as HPLC, GC, UV-Vis spectrophotometry, and Karl Fischer titrators. You will play a crucial role in identifying deviations from specifications, investigating out-of-specification (OOS) results, and contributing to corrective and preventive actions (CAPA). The ideal candidate will possess a strong academic background in Chemistry, Pharmacy, or a related life science discipline, coupled with extensive hands-on experience in pharmaceutical quality control. Proficiency with pharmacopeial methods (USP, EP, BP) is essential. This is a fully remote position, requiring exceptional organizational skills, self-motivation, and the ability to manage laboratory data and reports accurately from a remote location. You must possess excellent analytical thinking, attention to detail, and strong written and verbal communication skills to effectively document findings and collaborate with cross-functional teams, including R&D, manufacturing, and regulatory affairs. The ability to work independently and as a proactive member of a virtual team is paramount. You will contribute significantly to ensuring product quality and patient safety. This role offers an exciting opportunity to apply your expertise in a critical area of pharmaceutical development and manufacturing, all within a flexible remote work setting. Your insights will directly impact product release and regulatory submissions.
Responsibilities:
Responsibilities:
- Perform analytical testing on raw materials, intermediates, and finished pharmaceutical products.
- Execute method validation and transfer protocols.
- Operate and maintain analytical instrumentation (HPLC, GC, UV-Vis, KF).
- Interpret analytical data and prepare detailed test reports.
- Investigate out-of-specification (OOS) and out-of-trend (OOT) results.
- Contribute to the development and implementation of CAPAs.
- Ensure compliance with GLP, GMP, and relevant pharmacopeial standards.
- Review and approve analytical batch records.
- Collaborate with R&D, manufacturing, and regulatory teams.
- Participate in internal and external audits.
- 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/assurance.
- Extensive experience with analytical techniques (HPLC, GC, spectroscopy).
- Proficiency in pharmacopeial methods (USP, EP, BP).
- Strong understanding of GLP and GMP regulations.
- Excellent data analysis and problem-solving skills.
- Meticulous attention to detail and strong documentation abilities.
- Effective written and verbal communication skills.
- Proven ability to work independently and manage tasks in a remote environment.
This advertiser has chosen not to accept applicants from your region.
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Senior Pharmaceutical Quality Control Analyst (Remote)
Posted 21 days ago
Job Viewed
Job Description
Our client, a rapidly growing pharmaceutical company, is seeking a highly motivated and experienced Senior Pharmaceutical Quality Control Analyst to join their fully remote Quality Assurance team. This critical role involves ensuring the highest standards of quality and compliance across all pharmaceutical products. You will be responsible for developing, validating, and executing analytical methods, performing stability testing, and analyzing raw materials, intermediates, and finished products. The ideal candidate will possess a strong understanding of Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and relevant regulatory guidelines (e.g., FDA, EMA). Proficiency in various analytical techniques such as HPLC, GC, UV-Vis, and Karl Fischer titration is essential. You will play a key role in investigating deviations, Out-of-Specification (OOS) results, and implementing corrective and preventive actions (CAPA). This position requires meticulous attention to detail, strong problem-solving skills, and the ability to work independently in a remote setting. You will collaborate with cross-functional teams, including R&D, Manufacturing, and Regulatory Affairs, to ensure product quality and safety. The ability to interpret complex data, generate comprehensive reports, and contribute to continuous improvement initiatives is vital. This is an excellent opportunity to leverage your expertise in a challenging and rewarding remote environment. The original **job location** was specified as **Bungoma, Bungoma, KE**, however, this position is exclusively remote, allowing candidates to work from anywhere. We are looking for individuals with a passion for quality and a commitment to ensuring the efficacy and safety of pharmaceutical products.
Responsibilities:
Responsibilities:
- Develop, validate, and execute analytical methods for raw materials, in-process samples, and finished products.
- Perform routine and non-routine testing using techniques such as HPLC, GC, UV-Vis, FT-IR, and KF.
- Conduct stability studies according to established protocols.
- Analyze and interpret test data, preparing detailed reports of findings.
- Investigate deviations, OOS results, and customer complaints, implementing CAPAs.
- Ensure compliance with GMP, GLP, and other relevant regulatory standards.
- Calibrate and maintain laboratory equipment.
- Collaborate with R&D and manufacturing teams on product development and troubleshooting.
- Contribute to the continuous improvement of quality control processes and procedures.
- Prepare and review QC-related documentation.
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biotechnology, or a related life science field.
- Minimum of 5 years of experience in pharmaceutical quality control or assurance.
- Extensive hands-on experience with analytical instrumentation (HPLC, GC, etc.).
- In-depth knowledge of GMP, GLP, and relevant regulatory guidelines.
- Strong analytical, problem-solving, and critical thinking skills.
- Excellent written and verbal communication skills.
- Ability to work independently and manage time effectively in a remote setup.
This advertiser has chosen not to accept applicants from your region.
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Senior Pharmaceutical Quality Control Analyst (Remote)
Posted 20 days ago
Job Viewed
Job Description
Our client is seeking a highly experienced and meticulous Senior Pharmaceutical Quality Control Analyst to join their fully remote quality assurance team. This pivotal role involves ensuring the highest standards of quality and compliance for pharmaceutical products through rigorous testing and analysis. You will be instrumental in executing analytical methods, validating results, and contributing to the overall quality management system. This is an excellent opportunity for a seasoned QC professional to apply their expertise in a remote setting, contributing to the development and delivery of safe and effective medicines.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Perform a wide range of analytical tests on raw materials, in-process samples, and finished pharmaceutical products using various laboratory techniques (e.g., HPLC, GC, UV-Vis, spectroscopy, wet chemistry).
- Develop, validate, and implement new analytical methods according to regulatory guidelines (e.g., ICH, USP, EP).
- Analyze and interpret test results, ensuring accuracy and compliance with product specifications and regulatory requirements.
- Document all laboratory activities, results, and deviations meticulously in accordance with Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP).
- Troubleshoot and maintain laboratory equipment, ensuring proper calibration and functionality.
- Investigate out-of-specification (OOS) results and deviations, recommending corrective and preventive actions (CAPA).
- Review and approve batch records, Certificates of Analysis (CoA), and other quality-related documentation.
- Participate in internal and external audits, providing necessary documentation and explanations.
- Stay updated on current pharmaceutical regulations, quality standards, and industry best practices.
- Collaborate with R&D, production, and regulatory affairs teams to resolve quality issues.
- Mentor and train junior QC analysts, providing technical guidance and support.
Qualifications:
- Bachelor's or Master's degree in Pharmacy, Chemistry, Analytical Chemistry, or a related scientific discipline.
- Minimum of 6 years of hands-on experience in pharmaceutical quality control or a related analytical laboratory setting.
- Extensive experience with analytical instrumentation such as HPLC, GC, mass spectrometry, and spectrophotometry.
- In-depth knowledge of pharmaceutical quality systems, GMP, GLP, and relevant regulatory guidelines.
- Proven ability to develop, validate, and transfer analytical methods.
- Strong understanding of pharmacopeias (USP, EP, JP) and their requirements.
- Excellent analytical, problem-solving, and critical thinking skills.
- Meticulous attention to detail and strong documentation skills.
- Effective communication and interpersonal skills, with the ability to collaborate remotely.
- Proficiency in laboratory information management systems (LIMS) is desirable.
This advertiser has chosen not to accept applicants from your region.
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Senior Pharmaceutical Quality Control Analyst - Remote
Posted 21 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical innovator, is seeking an experienced Senior Pharmaceutical Quality Control Analyst to join their expanding remote team. This critical role will involve ensuring the highest standards of quality and compliance for our pharmaceutical products through rigorous remote analysis and reporting. You will be responsible for developing, validating, and implementing analytical methods, interpreting complex data, and ensuring all activities adhere to strict regulatory guidelines (e.g., GMP, ICH). The position demands a deep understanding of pharmaceutical manufacturing processes, analytical techniques, and quality management systems. You will conduct stability studies, perform raw material and finished product testing, and contribute to deviation investigations and CAPA (Corrective and Preventive Actions) management. Collaboration with cross-functional teams, including R&D, manufacturing, and regulatory affairs, will be a key aspect of your role, requiring excellent communication and interpersonal skills to effectively convey technical information and findings in a virtual setting. A strong commitment to scientific integrity and a meticulous approach to documentation are essential. The ideal candidate will possess advanced analytical skills, a proven ability to troubleshoot and solve complex problems, and a track record of successfully contributing to quality assurance initiatives. Experience with various analytical instrumentation (HPLC, GC, UV-Vis, IR, etc.) and data analysis software is required. This is a unique opportunity for a dedicated pharmaceutical professional to make a significant impact on product quality and patient safety while working in a flexible, remote environment. You will be empowered to drive quality initiatives and contribute to the continuous improvement of our pharmaceutical portfolio. The role requires self-motivation, excellent time management, and the ability to thrive in an independent work setting, with regular virtual interaction with colleagues and supervisors.
Responsibilities:
Responsibilities:
- Develop, validate, and implement analytical test methods for pharmaceutical products.
- Conduct raw material, in-process, and finished product testing.
- Analyze and interpret complex analytical data, generating comprehensive reports.
- Perform stability studies and monitor product shelf-life.
- Investigate deviations and contribute to CAPA development and implementation.
- Ensure compliance with GMP, ICH guidelines, and other relevant regulatory standards.
- Collaborate with R&D, manufacturing, and regulatory teams.
- Maintain detailed and accurate laboratory records and documentation.
- Operate and maintain analytical instrumentation (HPLC, GC, KF, etc.).
- Contribute to process improvements and quality initiatives.
- Bachelor's or Master's degree in Pharmacy, Chemistry, or a related life science field.
- Minimum of 5 years of experience in pharmaceutical quality control or assurance.
- Extensive knowledge of GMP and regulatory requirements.
- Proficiency in analytical techniques and instrumentation.
- Strong data analysis and interpretation skills.
- Excellent written and verbal communication skills.
- Ability to work independently and manage multiple projects remotely.
- Experience with LIMS and electronic data management systems is a plus.
This advertiser has chosen not to accept applicants from your region.
3
Senior Pharmaceutical Quality Control Analyst - Remote
Posted 22 days ago
Job Viewed
Job Description
Our client is seeking a highly experienced Senior Pharmaceutical Quality Control Analyst to lead critical quality assurance activities within our organization. This fully remote role is responsible for ensuring that all pharmaceutical products meet stringent quality standards and regulatory requirements throughout their lifecycle. You will perform advanced analytical testing, interpret complex data, and contribute to the development and validation of analytical methods. The ideal candidate will possess a deep understanding of pharmaceutical manufacturing processes, quality control principles, and relevant regulatory guidelines (e.g., GMP, ICH).
Key responsibilities include conducting various analytical tests using sophisticated laboratory equipment (e.g., HPLC, GC, UV-Vis spectrophotometry), analyzing test results, and generating comprehensive reports. You will be involved in method development and validation activities, ensuring accuracy and reliability of testing procedures. This role requires excellent scientific judgment, meticulous attention to detail, and the ability to troubleshoot analytical challenges independently. Strong collaboration skills are essential for working with R&D, manufacturing, and regulatory affairs teams to resolve quality issues and ensure product compliance. A Bachelor's or Master's degree in Pharmacy, Chemistry, or a related life science discipline, coupled with a minimum of 6 years of experience in pharmaceutical quality control and analysis, is required. Experience with data integrity principles and electronic laboratory notebooks (ELNs) is highly desirable. This remote position offers the opportunity to apply your expertise in a dynamic environment, contributing significantly to the safety and efficacy of pharmaceutical products. You will be instrumental in upholding the highest standards of quality and compliance.
This is a fully remote role, with no requirement to be present in Kisumu, Kisumu, KE.
Responsibilities:
Key responsibilities include conducting various analytical tests using sophisticated laboratory equipment (e.g., HPLC, GC, UV-Vis spectrophotometry), analyzing test results, and generating comprehensive reports. You will be involved in method development and validation activities, ensuring accuracy and reliability of testing procedures. This role requires excellent scientific judgment, meticulous attention to detail, and the ability to troubleshoot analytical challenges independently. Strong collaboration skills are essential for working with R&D, manufacturing, and regulatory affairs teams to resolve quality issues and ensure product compliance. A Bachelor's or Master's degree in Pharmacy, Chemistry, or a related life science discipline, coupled with a minimum of 6 years of experience in pharmaceutical quality control and analysis, is required. Experience with data integrity principles and electronic laboratory notebooks (ELNs) is highly desirable. This remote position offers the opportunity to apply your expertise in a dynamic environment, contributing significantly to the safety and efficacy of pharmaceutical products. You will be instrumental in upholding the highest standards of quality and compliance.
This is a fully remote role, with no requirement to be present in Kisumu, Kisumu, KE.
Responsibilities:
- Perform analytical testing on raw materials, intermediates, and finished pharmaceutical products.
- Operate and maintain analytical laboratory instruments (HPLC, GC, UV-Vis, etc.).
- Analyze test data, interpret results, and generate accurate reports.
- Develop, validate, and transfer analytical methods according to regulatory guidelines.
- Ensure compliance with Good Manufacturing Practices (GMP) and other relevant regulations.
- Troubleshoot analytical issues and implement corrective actions.
- Participate in stability studies and environmental monitoring programs.
- Contribute to quality risk assessments and investigations.
- Maintain detailed and accurate laboratory records.
- Collaborate with cross-functional teams on quality-related matters.
- Bachelor's or Master's degree in Pharmacy, Chemistry, or related life science.
- Minimum of 6 years of experience in pharmaceutical quality control.
- Extensive experience with analytical techniques (HPLC, GC, UV-Vis).
- Strong knowledge of GMP, ICH guidelines, and pharmacopeial standards.
- Experience in method development and validation.
- Excellent analytical, problem-solving, and documentation skills.
- Ability to work independently and manage time effectively in a remote setting.
This advertiser has chosen not to accept applicants from your region.
4
Senior Pharmaceutical Quality Control Analyst (Remote)
Posted 22 days ago
Job Viewed
Job Description
Our client, a leading innovator in pharmaceutical development, is seeking a highly skilled and motivated Senior Pharmaceutical Quality Control Analyst to join their dynamic, fully remote team. This pivotal role is crucial in ensuring the consistent quality and safety of our pharmaceutical products, from raw materials to finished goods. You will be responsible for developing, validating, and implementing analytical methods, performing complex tests, and meticulously documenting all results. The ideal candidate will possess a deep understanding of GMP (Good Manufacturing Practices) and regulatory requirements within the pharmaceutical industry. You will work collaboratively with R&D, manufacturing, and regulatory affairs departments to resolve quality issues and drive continuous improvement initiatives. Your responsibilities will include conducting stability studies, analyzing product samples using various advanced analytical techniques such as HPLC, GC, UV-Vis, and Karl Fischer titration, and interpreting data to make informed decisions. Furthermore, you will be tasked with troubleshooting analytical instrumentation, maintaining laboratory equipment, and ensuring compliance with all safety and environmental regulations. This is a remote-first position, demanding excellent communication skills and the ability to work independently with minimal supervision. You will be expected to participate actively in virtual team meetings, contribute to project planning, and maintain accurate records within our digital systems. The ability to manage multiple projects simultaneously and meet strict deadlines is essential. A Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or a related field is required, along with a minimum of 5 years of experience in pharmaceutical quality control. Experience with data integrity principles and electronic laboratory notebooks (ELN) is highly desirable. Join us and play a key role in delivering life-saving medicines to patients worldwide, from the comfort of your home office in or near Ongata Rongai, Kajiado, KE .
This advertiser has chosen not to accept applicants from your region.
5
Senior Pharmaceutical Quality Control Analyst - Remote
Posted 22 days ago
Job Viewed
Job Description
Our client is seeking a highly meticulous and experienced Senior Pharmaceutical Quality Control Analyst to join their fully remote quality assurance team. This vital role focuses on ensuring the quality and compliance of pharmaceutical products through rigorous testing and analysis. You will be responsible for developing and validating analytical methods, conducting routine quality control testing, and interpreting results according to established protocols and regulatory guidelines (e.g., GMP, GLP). The ideal candidate will possess a strong scientific background, exceptional attention to detail, and a deep understanding of analytical chemistry techniques. Key responsibilities include performing stability studies, analyzing raw materials, in-process samples, and finished products, and documenting all testing procedures and results accurately. You will also play a role in investigating deviations, out-of-specification (OOS) results, and implementing corrective and preventive actions (CAPA). Experience with various analytical instruments such as HPLC, GC, UV-Vis spectrophotometers, and dissolution apparatus is essential. This is a remote-first position requiring strong self-discipline, excellent scientific communication skills, and the ability to work independently while collaborating effectively with laboratory and regulatory teams. Your contribution will be critical to maintaining the highest standards of pharmaceutical quality and safety.
Responsibilities:
Qualifications:
This fully remote role offers a unique opportunity for skilled QC professionals to apply their expertise within the pharmaceutical sector, contributing to product safety and efficacy from any location within Kenya.
Responsibilities:
- Perform analytical testing of raw materials, in-process samples, and finished pharmaceutical products.
- Develop, validate, and transfer analytical methods according to regulatory standards.
- Operate and maintain laboratory equipment such as HPLC, GC, and spectrophotometers.
- Interpret analytical data and generate detailed reports.
- Investigate out-of-specification (OOS) results and deviations, and implement CAPA.
- Ensure compliance with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).
- Participate in stability studies and analyze results.
- Maintain accurate and comprehensive laboratory records.
- Review and approve quality control documentation.
- Contribute to the continuous improvement of QC processes and procedures.
Qualifications:
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biochemistry, or a related scientific discipline.
- Minimum of 5 years of experience in pharmaceutical quality control or quality assurance.
- Proven experience with analytical techniques and instrumentation (HPLC, GC, UV-Vis, Dissolution).
- In-depth knowledge of pharmaceutical quality systems and regulatory requirements (GMP, ICH).
- Strong understanding of analytical method development and validation.
- Excellent data analysis, problem-solving, and critical thinking skills.
- Meticulous attention to detail and commitment to accuracy.
- Effective written and verbal communication skills, suited for remote scientific communication.
- Ability to work independently and manage laboratory tasks in a remote setting.
- Experience with LIMS (Laboratory Information Management System) is a plus.
This fully remote role offers a unique opportunity for skilled QC professionals to apply their expertise within the pharmaceutical sector, contributing to product safety and efficacy from any location within Kenya.
This advertiser has chosen not to accept applicants from your region.
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6
Senior Pharmaceutical Quality Control Analyst - Remote
Posted 6 days ago
Job Viewed
Job Description
Our client, a reputable pharmaceutical company, is actively seeking an experienced Senior Pharmaceutical Quality Control Analyst to join their esteemed, fully remote team. This vital role is responsible for ensuring the quality and integrity of pharmaceutical products through rigorous testing and analysis. The ideal candidate will possess a strong background in analytical chemistry, quality control methodologies, and regulatory compliance within the pharmaceutical industry. You will perform a wide range of laboratory tests, analyze data, document findings, and contribute to the continuous improvement of quality assurance processes, all while working remotely. This position requires meticulous attention to detail, a commitment to scientific accuracy, and the ability to manage tasks independently.
Key Responsibilities:
Qualifications:
This is an exceptional opportunity for a seasoned Quality Control Analyst to advance their career while enjoying the benefits of a fully remote role. Our client is dedicated to upholding the highest standards of pharmaceutical quality and safety and seeks a candidate who shares this commitment.
Key Responsibilities:
- Conduct comprehensive analytical testing of raw materials, in-process samples, and finished pharmaceutical products using various instrumental and wet chemistry techniques.
- Interpret test results, analyze data, and prepare detailed analytical reports.
- Ensure all testing activities comply with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant regulatory guidelines.
- Calibrate, maintain, and troubleshoot laboratory equipment to ensure accurate and reliable results.
- Develop and validate analytical methods as needed.
- Investigate deviations and out-of-specification (OOS) results, documenting findings and recommending corrective and preventive actions (CAPAs).
- Participate in internal and external audits related to quality control.
- Maintain accurate and organized laboratory records and documentation.
- Collaborate with other departments, such as R&D and manufacturing, to address quality-related issues.
- Stay updated on industry trends, regulatory changes, and advancements in analytical techniques.
Qualifications:
- Bachelor's degree in Chemistry, Pharmaceutical Sciences, or a related scientific discipline. A Master's degree is a plus.
- Minimum of 5 years of experience in pharmaceutical quality control or analytical development.
- Proficiency in performing a variety of analytical techniques, including HPLC, GC, UV-Vis spectroscopy, FTIR, and dissolution testing.
- In-depth knowledge of GMP, GLP, and relevant pharmaceutical regulatory requirements (e.g., FDA, EMA).
- Experience with laboratory information management systems (LIMS) and electronic data capture.
- Strong analytical, problem-solving, and critical thinking skills.
- Excellent written and verbal communication skills, with the ability to document procedures and results clearly and concisely.
- Demonstrated ability to work independently and manage time effectively in a remote work environment.
- Meticulous attention to detail and a commitment to accuracy.
- Ability to collaborate effectively with remote team members.
This is an exceptional opportunity for a seasoned Quality Control Analyst to advance their career while enjoying the benefits of a fully remote role. Our client is dedicated to upholding the highest standards of pharmaceutical quality and safety and seeks a candidate who shares this commitment.
This advertiser has chosen not to accept applicants from your region.
7
Senior Pharmaceutical Quality Control Analyst (Remote)
Posted 8 days ago
Job Viewed
Job Description
Our client is seeking a highly experienced Senior Pharmaceutical Quality Control Analyst to join their fully remote Quality Assurance team. This critical role involves ensuring the quality and integrity of pharmaceutical products through rigorous testing and analysis. You will be responsible for developing and implementing quality control procedures, performing analytical testing, and maintaining compliance with regulatory standards. This is an excellent opportunity for a skilled professional to contribute to the pharmaceutical industry from a remote setting, ensuring the safety and efficacy of vital medications. You will work with a dedicated team focused on upholding the highest standards of pharmaceutical quality.
Key responsibilities include:
The ideal candidate will hold a Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or a related field, with a minimum of 7 years of progressive experience in pharmaceutical quality control. A strong background in analytical method development and validation, and extensive hands-on experience with chromatography (HPLC, GC) and spectroscopy techniques are essential. Knowledge of Good Manufacturing Practices (GMP) and relevant regulatory requirements is mandatory. Excellent analytical, problem-solving, and documentation skills are critical for success in this fully remote role. Strong organizational skills and the ability to manage workload effectively in a remote environment are required. Our client offers a competitive salary, comprehensive benefits, and the opportunity to make a significant contribution to pharmaceutical quality.
Key responsibilities include:
- Developing, validating, and implementing analytical test methods for raw materials, in-process samples, and finished products.
- Performing quantitative and qualitative analyses using a variety of analytical techniques (e.g., HPLC, GC, spectroscopy, titrations).
- Interpreting test results and comparing them against established specifications and acceptance criteria.
- Documenting all laboratory activities, test results, and deviations accurately and thoroughly in compliance with GMP.
- Investigating out-of-specification (OOS) results and implementing corrective and preventive actions (CAPA).
- Maintaining laboratory equipment, performing calibrations, and ensuring adherence to safety protocols.
- Contributing to the development and maintenance of Standard Operating Procedures (SOPs) for the QC laboratory.
- Staying current with regulatory guidelines (e.g., FDA, EMA) and industry best practices in pharmaceutical quality control.
- Collaborating with R&D, manufacturing, and regulatory affairs teams in a remote capacity.
- Participating in internal and external audits.
- Training and mentoring junior QC analysts.
The ideal candidate will hold a Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or a related field, with a minimum of 7 years of progressive experience in pharmaceutical quality control. A strong background in analytical method development and validation, and extensive hands-on experience with chromatography (HPLC, GC) and spectroscopy techniques are essential. Knowledge of Good Manufacturing Practices (GMP) and relevant regulatory requirements is mandatory. Excellent analytical, problem-solving, and documentation skills are critical for success in this fully remote role. Strong organizational skills and the ability to manage workload effectively in a remote environment are required. Our client offers a competitive salary, comprehensive benefits, and the opportunity to make a significant contribution to pharmaceutical quality.
This advertiser has chosen not to accept applicants from your region.
8
Senior Pharmaceutical Quality Control Analyst (Remote)
Posted 5 days ago
Job Viewed
Job Description
Our client, a dynamic pharmaceutical research and development company, is seeking a highly skilled and experienced Senior Pharmaceutical Quality Control Analyst to join their 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. Your duties will encompass developing and validating analytical methods, performing routine testing of raw materials, in-process samples, and finished products using advanced laboratory techniques and instrumentation (e.g., HPLC, GC, spectroscopy). You will meticulously document all experimental procedures, results, and deviations in accordance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). A significant part of your role will involve investigating out-of-specification (OOS) results, identifying root causes, and recommending corrective and preventive actions (CAPAs). You will contribute to the preparation of regulatory submission documents and collaborate with cross-functional teams, including R&D, manufacturing, and regulatory affairs, to resolve quality issues. The ideal candidate will possess a Bachelor's or Master's degree in Pharmacy, Chemistry, or a related scientific field, coupled with a minimum of 5 years of progressive experience in pharmaceutical quality control. Proficiency in data analysis and interpretation, strong problem-solving abilities, and excellent written and verbal communication skills are essential. This remote position requires a high degree of autonomy, self-discipline, and the ability to manage multiple projects effectively. You will play a vital role in safeguarding public health by ensuring that all products meet the highest quality and safety standards. The work is conceptually associated with **Ongata Rongai, Kajiado, KE**, but will be performed entirely remotely.
This advertiser has chosen not to accept applicants from your region.
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