37 Remote Pharmaceutical Quality Control Analyst jobs in whatjobs
Remote Pharmaceutical Quality Control Analyst
Posted 21 days ago
Job Viewed
Job Description
Our client, a cutting-edge pharmaceutical company, is seeking a detail-oriented and experienced Remote Pharmaceutical Quality Control Analyst to join their highly regulated team. This fully remote position offers the unique opportunity to contribute to ensuring the highest standards of pharmaceutical product quality and safety from your home laboratory or office setup. You will be instrumental in conducting analytical testing, interpreting results, and ensuring compliance with stringent regulatory guidelines.
Key Responsibilities:
Qualifications:
This is an exceptional opportunity for a Pharmaceutical Quality Control Analyst seeking a remote position that allows them to apply their expertise to critical quality assurance processes. If you are passionate about pharmaceutical quality and possess the technical skills and independent work ethic required for a remote role, we encourage you to apply. Join a forward-thinking company dedicated to advancing healthcare through quality products.
Key Responsibilities:
- Perform a variety of analytical tests on raw materials, in-process samples, and finished pharmaceutical products using advanced laboratory techniques and equipment.
- Analyze test results, compare them against established specifications, and document findings meticulously.
- Identify and investigate any deviations from quality standards, initiating corrective and preventive actions (CAPA) as needed.
- Ensure all laboratory activities comply with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant regulatory requirements.
- Maintain and calibrate laboratory equipment to ensure accuracy and reliability of results.
- Prepare technical reports, summaries, and documentation related to quality control testing.
- Participate in method validation and transfer activities.
- Collaborate with cross-functional teams, including R&D, manufacturing, and regulatory affairs, in a remote setting.
- Contribute to the continuous improvement of quality control processes and procedures.
- Stay updated on scientific advancements and regulatory changes impacting pharmaceutical quality control.
Qualifications:
- Bachelor's or Master's degree in Pharmacy, Chemistry, Pharmaceutical Sciences, or a related scientific discipline.
- Minimum of 3-5 years of experience in pharmaceutical quality control or a related laboratory role.
- Strong knowledge of analytical techniques commonly used in the pharmaceutical industry (e.g., HPLC, GC, spectroscopy).
- Familiarity with GMP, GLP, and other regulatory guidelines (FDA, EMA).
- Excellent analytical, problem-solving, and critical thinking skills.
- Proficiency in data analysis and scientific report writing.
- Strong attention to detail and commitment to accuracy.
- Effective communication and collaboration skills suitable for a remote work environment.
- Ability to work independently, manage time efficiently, and maintain high productivity in a remote setting.
- Experience with LIMS (Laboratory Information Management System) is a plus.
- Access to a suitable home laboratory space with necessary equipment or willingness to establish one may be required based on specific project needs.
This is an exceptional opportunity for a Pharmaceutical Quality Control Analyst seeking a remote position that allows them to apply their expertise to critical quality assurance processes. If you are passionate about pharmaceutical quality and possess the technical skills and independent work ethic required for a remote role, we encourage you to apply. Join a forward-thinking company dedicated to advancing healthcare through quality products.
This advertiser has chosen not to accept applicants from your region.
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Remote Pharmaceutical Quality Control Analyst
Posted 20 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical innovator, is looking for an experienced Pharmaceutical Quality Control Analyst to join their remote team. This role is crucial in ensuring the integrity and safety of pharmaceutical products by meticulously analyzing raw materials, in-process samples, and finished goods. As a remote analyst, you will leverage advanced analytical techniques and state-of-the-art laboratory equipment (which will be provided or access facilitated remotely) to perform a wide range of tests. Your responsibilities will include meticulously documenting all experimental procedures, results, and deviations according to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). You will interpret complex data, identify trends, and contribute to the resolution of quality issues. This position requires a strong foundation in analytical chemistry, spectroscopy, chromatography, and other relevant pharmaceutical testing methodologies. The ability to work independently, manage your time effectively, and maintain strict adherence to quality standards is paramount. You will collaborate with R&D, manufacturing, and regulatory affairs teams via virtual communication channels to ensure product compliance and continuous improvement. The ideal candidate possesses excellent problem-solving skills, a keen eye for detail, and a robust understanding of the pharmaceutical regulatory landscape. Although the role is fully remote, a foundational understanding of pharmaceutical operations, potentially including those relevant to areas like Machakos, Machakos, KE , is beneficial. This is an exceptional opportunity to contribute to life-saving medicines from the comfort of your home office.
This advertiser has chosen not to accept applicants from your region.
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Remote Pharmaceutical Quality Control Analyst
Posted 21 days ago
Job Viewed
Job Description
Our client is seeking a meticulous and highly qualified Pharmaceutical Quality Control Analyst to join their esteemed team. This fully remote position requires an individual with a strong understanding of pharmaceutical manufacturing processes and stringent quality assurance standards. You will be responsible for conducting various laboratory tests and analyses on raw materials, in-process samples, and finished pharmaceutical products to ensure they meet all regulatory and internal quality specifications. Your role is critical in maintaining the integrity and safety of the medicines produced.
Key responsibilities include performing analytical testing using a range of laboratory equipment and techniques, such as High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), and spectroscopy. You will accurately document all test results, maintain detailed records, and prepare comprehensive reports. Adherence to Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) is paramount. You will participate in method validation activities, troubleshoot analytical methods, and contribute to the continuous improvement of quality control procedures. The ability to work independently, manage your time effectively, and communicate findings clearly is essential for this remote role. You will collaborate closely with production, R&D, and regulatory affairs departments to address any quality deviations or issues. A proactive approach to identifying potential risks and implementing preventative measures is highly valued. This position offers an exciting opportunity to contribute to the pharmaceutical industry from the convenience of your home office, playing a vital role in delivering safe and effective pharmaceutical products to the market. Your expertise will directly impact product quality and patient safety.
Location: This is a fully remote position, allowing you to work from anywhere.
Qualifications:
Key responsibilities include performing analytical testing using a range of laboratory equipment and techniques, such as High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), and spectroscopy. You will accurately document all test results, maintain detailed records, and prepare comprehensive reports. Adherence to Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) is paramount. You will participate in method validation activities, troubleshoot analytical methods, and contribute to the continuous improvement of quality control procedures. The ability to work independently, manage your time effectively, and communicate findings clearly is essential for this remote role. You will collaborate closely with production, R&D, and regulatory affairs departments to address any quality deviations or issues. A proactive approach to identifying potential risks and implementing preventative measures is highly valued. This position offers an exciting opportunity to contribute to the pharmaceutical industry from the convenience of your home office, playing a vital role in delivering safe and effective pharmaceutical products to the market. Your expertise will directly impact product quality and patient safety.
Location: This is a fully remote position, allowing you to work from anywhere.
Qualifications:
- Bachelor's degree in Pharmacy, Chemistry, Biochemistry, or a related life science discipline.
- Minimum of 3 years of experience in pharmaceutical quality control or quality assurance.
- Hands-on experience with analytical instrumentation such as HPLC, GC, UV-Vis spectrophotometry.
- Strong knowledge of GMP, GLP, and relevant pharmaceutical regulatory guidelines.
- Experience in method development and validation.
- Excellent data analysis, documentation, and report-writing skills.
- Proficiency in laboratory information management systems (LIMS).
- Ability to work independently and manage multiple tasks effectively in a remote environment.
- Strong problem-solving skills and attention to detail.
This advertiser has chosen not to accept applicants from your region.
2
Remote Pharmaceutical Quality Control Analyst
Posted 22 days ago
Job Viewed
Job Description
Our client is seeking a highly meticulous and detail-oriented Remote Pharmaceutical Quality Control Analyst to ensure the highest standards of product quality and compliance. This is a critical role within a fully remote setup, allowing you to contribute to vital quality assurance processes from the comfort of your home office. The successful candidate will be responsible for conducting rigorous testing and analysis of pharmaceutical raw materials, in-process samples, and finished products. You will interpret test results, document findings accurately, and identify any deviations from established specifications. This role involves utilizing sophisticated laboratory equipment and analytical techniques, adhering strictly to Good Manufacturing Practices (GMP) and other relevant regulatory guidelines. A significant part of your responsibility will be to contribute to the continuous improvement of quality control procedures and participate in investigations of out-of-specification results. We are looking for an individual with a strong scientific background, excellent analytical skills, and a thorough understanding of pharmaceutical quality systems. The ability to work independently, manage your workload efficiently, and maintain accurate records in a remote environment is paramount. Strong written and verbal communication skills are essential for reporting findings and collaborating with cross-functional teams. If you are passionate about ensuring drug safety and efficacy and thrive in a remote, research-driven setting, this opportunity is ideal for you. Your contributions will be vital in maintaining our client's commitment to producing safe and effective pharmaceutical products.
This advertiser has chosen not to accept applicants from your region.
3
Remote Pharmaceutical Quality Control Analyst
Posted 8 days ago
Job Viewed
Job Description
Our client, a dynamic pharmaceutical company, is seeking a meticulous and experienced Pharmaceutical Quality Control Analyst for a fully remote position. This role is critical in ensuring the quality and compliance of pharmaceutical products throughout their lifecycle. You will be responsible for reviewing and analyzing quality control data, evaluating test results against established specifications, and contributing to the development and validation of analytical methods. 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 analytical techniques such as HPLC, GC, UV-Vis spectroscopy, and dissolution testing is essential. You will conduct thorough investigations into deviations and out-of-specification results, recommending and implementing corrective and preventive actions (CAPAs). This position requires excellent attention to detail, strong problem-solving skills, and the ability to interpret complex scientific data. You will collaborate with R&D, manufacturing, and regulatory affairs teams using advanced digital collaboration tools. A Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field is required, along with substantial experience in pharmaceutical quality control or assurance. The ability to work independently, manage multiple projects, and meet stringent deadlines in a remote setting is crucial. This is a unique opportunity to contribute to public health by ensuring the highest standards of pharmaceutical quality from a remote location. The job is situated in Bungoma, Bungoma, KE , but this is a completely remote role.
This advertiser has chosen not to accept applicants from your region.
4
Remote Pharmaceutical Quality Control Analyst
Posted 8 days ago
Job Viewed
Job Description
Our client, a reputable pharmaceutical company, is seeking a meticulous and experienced Remote Pharmaceutical Quality Control Analyst. This position is entirely remote, focusing on ensuring the highest standards of quality and compliance for pharmaceutical products from a distance. You will be responsible for reviewing and analyzing quality control data, investigating deviations, and contributing to the continuous improvement of quality systems. The ideal candidate will have a solid understanding of Good Manufacturing Practices (GMP), pharmaceutical testing methodologies, and regulatory requirements. This role requires exceptional attention to detail, strong analytical skills, and the ability to effectively communicate findings and recommendations in a virtual setting.
Responsibilities:
Responsibilities:
- Review and interpret analytical data from various quality control tests (e.g., HPLC, GC, spectroscopy) for raw materials, intermediates, and finished products.
- Investigate Out-of-Specification (OOS) results and deviations, identifying root causes and implementing corrective and preventive actions (CAPA).
- Ensure all quality control activities comply with GMP guidelines and regulatory standards.
- Prepare and review batch record documentation, certificates of analysis (CoA), and other quality-related documents.
- Participate in internal and external audits as a subject matter expert on quality control processes.
- Contribute to the development and validation of new analytical methods.
- Monitor quality trends and provide regular reports on key quality indicators.
- Collaborate with manufacturing, R&D, and regulatory affairs teams to resolve quality issues.
- Maintain a high level of proficiency in quality control procedures and instrumentation.
- Contribute to the continuous improvement of the company's quality management system.
- Bachelor's degree in Pharmacy, Chemistry, Biochemistry, or a related life science field.
- Minimum of 3 years of experience in pharmaceutical quality control or quality assurance.
- Strong knowledge of GMP, ICH guidelines, and other relevant regulatory requirements.
- Hands-on experience with common pharmaceutical analytical techniques (e.g., HPLC, UV-Vis, dissolution testing).
- Proficiency in data analysis and interpretation.
- Excellent written and verbal communication skills, with the ability to document findings clearly and concisely.
- Strong organizational and time management skills, essential for remote work.
- Ability to work independently with minimal supervision.
- Detail-oriented with a high degree of accuracy.
- Familiarity with quality management software is a plus.
This advertiser has chosen not to accept applicants from your region.
5
Remote Pharmaceutical Quality Control Analyst
Posted 7 days ago
Job Viewed
Job Description
Our client is seeking a meticulous and experienced Remote Pharmaceutical Quality Control Analyst to join their innovative research and development team. This fully remote position requires a deep understanding of pharmaceutical quality standards and analytical techniques. The ideal candidate will be responsible for ensuring the quality and integrity of pharmaceutical products by conducting rigorous testing and analysis from a remote location. This role demands exceptional attention to detail, a strong scientific background, and the ability to work autonomously. Responsibilities:
- Perform analytical testing on raw materials, in-process samples, and finished pharmaceutical products using various laboratory techniques (e.g., HPLC, GC, UV-Vis spectroscopy).
- Analyze test results, interpret data, and prepare comprehensive reports.
- Ensure all testing activities comply with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and regulatory guidelines (e.g., FDA, EMA).
- Maintain laboratory equipment and instruments, ensuring proper calibration and functionality.
- Investigate deviations from established procedures and specifications, identifying root causes and recommending corrective actions.
- Contribute to the development and validation of new analytical methods.
- Review and approve batch records and quality control documentation.
- Stay updated on the latest scientific advancements and regulatory requirements in the pharmaceutical industry.
- Collaborate with R&D, manufacturing, and regulatory affairs teams to address quality issues.
- Maintain accurate and detailed records of all experiments, analyses, and results in compliance with quality standards.
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field.
- Minimum of 4 years of experience in pharmaceutical quality control or a similar analytical laboratory setting.
- Extensive experience with analytical instrumentation and methodologies common in the pharmaceutical industry.
- Thorough understanding of GMP, GLP, and relevant regulatory requirements.
- Strong data analysis and interpretation skills.
- Excellent written and verbal communication skills, with the ability to produce clear and concise reports.
- Proven ability to work independently, manage time effectively, and meet deadlines in a remote environment.
- Meticulous attention to detail and a commitment to accuracy and precision.
- Experience with method validation is highly desirable.
- Access to a suitable home laboratory setup or ability to work effectively with external accredited labs as needed.
This advertiser has chosen not to accept applicants from your region.
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Remote Pharmaceutical Quality Control Analyst
Posted 5 days ago
Job Viewed
Job Description
Our client, a growing pharmaceutical company, is seeking a diligent and detail-oriented Remote Pharmaceutical Quality Control Analyst to join their team. This fully remote position allows you to contribute significantly to ensuring the quality and safety of pharmaceutical products from the comfort of your home office. You will be responsible for reviewing and analyzing quality control data, ensuring compliance with regulatory standards, and supporting the overall quality management system. The ideal candidate possesses a strong background in pharmaceutical sciences, meticulous analytical skills, and a thorough understanding of GMP and regulatory requirements.
Responsibilities:
Responsibilities:
- Review and analyze data from various quality control tests performed on raw materials, in-process samples, and finished products.
- Ensure all testing is conducted according to approved standard operating procedures (SOPs) and Good Manufacturing Practices (GMP).
- Prepare, review, and approve quality control reports, certificates of analysis (CoAs), and related documentation.
- Investigate deviations and out-of-specification (OOS) results, identifying root causes and recommending corrective actions.
- Monitor and maintain laboratory equipment calibration and qualification records.
- Assist in the preparation for and participation in regulatory inspections and audits.
- Contribute to the continuous improvement of quality control processes and systems.
- Maintain accurate and organized records in compliance with pharmaceutical industry standards.
- Collaborate effectively with remote colleagues in manufacturing, R&D, and regulatory affairs.
- Stay updated on current regulatory guidelines and industry best practices related to pharmaceutical quality control.
- Bachelor's degree in Pharmacy, Chemistry, Biochemistry, Microbiology, or a related pharmaceutical science field.
- Minimum of 5 years of experience in pharmaceutical quality control or quality assurance.
- Strong understanding of GMP, ICH guidelines, and other relevant regulatory requirements.
- Proficiency in analytical techniques commonly used in pharmaceutical QC (e.g., HPLC, GC, spectroscopy).
- Excellent data review, analytical, and problem-solving skills.
- Meticulous attention to detail and a commitment to accuracy.
- Strong written and verbal communication skills, adapted for remote interaction.
- Ability to manage multiple tasks and prioritize effectively in a remote work setting.
- Experience with pharmacopoeial standards (USP, EP, BP) is essential.
- Familiarity with pharmaceutical manufacturing processes relevant to regions like Bungoma, Bungoma, KE is an advantage.
This advertiser has chosen not to accept applicants from your region.
7
Remote Pharmaceutical Quality Control Analyst
Posted 5 days ago
Job Viewed
Job Description
Our client, a rapidly expanding pharmaceutical manufacturing company, is actively seeking a meticulous and experienced Pharmaceutical Quality Control Analyst to join their dedicated team. This critical role operates entirely remotely, allowing talented professionals to contribute to ensuring the highest standards of pharmaceutical product quality from their own home offices. The analyst will be instrumental in executing laboratory tests, analyzing results, and contributing to the overall quality assurance framework of the company's innovative product lines.
Key Responsibilities:
Qualifications:
This is a significant opportunity for a skilled QC professional to advance their career within a leading pharmaceutical entity. The role is fully remote and based in the vicinity of Mlolongo, Machakos, KE , offering a competitive salary and benefits, with the flexibility of a home-based work arrangement.
Key Responsibilities:
- Perform a variety of analytical tests on raw materials, in-process samples, and finished pharmaceutical products using established methodologies and state-of-the-art equipment.
- Accurately record and document all test results, observations, and deviations in accordance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
- Analyze test data to determine product conformance to specifications, identifying any out-of-specification (OOS) results.
- Troubleshoot and maintain laboratory equipment, ensuring its proper functioning and calibration.
- Participate in method validation and verification activities.
- Assist in the investigation of product quality complaints and deviations.
- Prepare and review Quality Control (QC) documentation, including test methods, standard operating procedures (SOPs), and reports.
- Collaborate with Research and Development (R&D) and Production teams to ensure seamless product lifecycle management.
- Maintain a safe and organized laboratory environment, adhering to all safety protocols.
- Contribute to continuous improvement initiatives within the QC department.
- Ensure compliance with all relevant regulatory guidelines (e.g., Pharmacy and Poisons Board regulations).
Qualifications:
- A Bachelor's degree in Pharmacy, Chemistry, Biochemistry, Biotechnology, or a related scientific field.
- Minimum of 3 years of hands-on experience in a pharmaceutical Quality Control laboratory setting.
- Strong understanding of analytical techniques such as HPLC, GC, UV-Vis spectrophotometry, and dissolution testing.
- Proficiency in Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
- Experience with OOS investigations and CAPA (Corrective and Preventive Actions).
- Excellent analytical, problem-solving, and critical thinking skills.
- Meticulous attention to detail and accuracy in data recording and reporting.
- Strong written and verbal communication skills.
- Ability to work independently with minimal supervision in a remote setting.
- Proficiency in Microsoft Office Suite.
- Knowledge of regulatory requirements for pharmaceutical products in Kenya is a plus.
This is a significant opportunity for a skilled QC professional to advance their career within a leading pharmaceutical entity. The role is fully remote and based in the vicinity of Mlolongo, Machakos, KE , offering a competitive salary and benefits, with the flexibility of a home-based work arrangement.
This advertiser has chosen not to accept applicants from your region.
8
Remote Pharmaceutical Quality Control Analyst
Posted 6 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is seeking a highly meticulous and skilled Remote Pharmaceutical Quality Control Analyst. This is a crucial, fully remote position focused on ensuring the quality and integrity of pharmaceutical products through remote analysis and documentation review. You will be responsible for performing various quality control tests, analyzing data, and ensuring compliance with stringent regulatory standards. This role requires a strong scientific background, excellent analytical abilities, and a keen eye for detail, all executed within a remote work framework.
Key responsibilities include:
The ideal candidate will possess a Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific discipline. A Master's degree is a plus. Proven experience in pharmaceutical quality control or quality assurance is essential. Strong knowledge of analytical techniques, GMP, and regulatory requirements in the pharmaceutical industry is mandatory. Excellent data analysis, problem-solving, and report-writing skills are critical. Proficiency with laboratory information management systems (LIMS) and standard office software is required. You must be highly organized, detail-oriented, and capable of working independently and managing your time effectively in a remote setting. Excellent written and verbal communication skills are necessary for effective remote collaboration. This role offers a significant opportunity to contribute to the safety and efficacy of pharmaceutical products from a remote capacity.
Key responsibilities include:
- Reviewing and analyzing quality control data from laboratory tests on raw materials, in-process samples, and finished products.
- Ensuring all testing and analysis comply with Good Manufacturing Practices (GMP) and other regulatory guidelines.
- Interpreting test results and identifying any deviations from specifications.
- Documenting all quality control activities accurately and comprehensively.
- Preparing reports on quality control findings and recommending corrective actions when necessary.
- Collaborating with R&D, manufacturing, and regulatory affairs teams remotely to address quality issues.
- Maintaining laboratory equipment calibration and validation records.
- Participating in the investigation of Out-of-Specification (OOS) results and deviations.
- Assisting in the validation of analytical methods.
- Staying current with pharmacopeial standards and regulatory updates.
- Contributing to the continuous improvement of quality control processes.
- Managing and organizing retained samples and reference standards.
- Performing trend analysis on quality control data to identify potential risks.
- Reviewing batch records and associated documentation for completeness and accuracy.
- Providing remote support for quality audits and inspections.
The ideal candidate will possess a Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific discipline. A Master's degree is a plus. Proven experience in pharmaceutical quality control or quality assurance is essential. Strong knowledge of analytical techniques, GMP, and regulatory requirements in the pharmaceutical industry is mandatory. Excellent data analysis, problem-solving, and report-writing skills are critical. Proficiency with laboratory information management systems (LIMS) and standard office software is required. You must be highly organized, detail-oriented, and capable of working independently and managing your time effectively in a remote setting. Excellent written and verbal communication skills are necessary for effective remote collaboration. This role offers a significant opportunity to contribute to the safety and efficacy of pharmaceutical products from a remote capacity.
This advertiser has chosen not to accept applicants from your region.
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