2 Remote Senior Pharmaceutical Quality Control Analyst jobs in whatjobs
Senior Pharmaceutical Quality Control Analyst
Posted 19 days ago
Job Viewed
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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Senior Pharmaceutical Quality Control Analyst
Posted 9 days ago
Job Viewed
Job Description
Our client, a prominent entity in the pharmaceutical industry, is seeking a highly skilled and meticulous Senior Pharmaceutical Quality Control Analyst to join our remote-based quality assurance team. This role is critical in ensuring the integrity, safety, and efficacy of our pharmaceutical products through rigorous testing and analysis. You will be responsible for performing a wide range of analytical tests on raw materials, in-process samples, and finished products using sophisticated laboratory equipment such as HPLC, GC, UV-Vis spectrophotometers, and dissolution apparatus. Your duties will include method development and validation, data interpretation, deviation investigation, and the preparation of detailed analytical reports. Strict adherence to Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and all relevant regulatory guidelines (e.g., FDA, EMA) is paramount. The ideal candidate will possess strong analytical chemistry skills, a deep understanding of pharmaceutical quality control principles, and extensive experience with various analytical techniques. Proficiency in LIMS (Laboratory Information Management System) and strong documentation skills are essential. You must be able to work independently, manage your time effectively, and collaborate seamlessly with remote colleagues and cross-functional teams. A Bachelor's or Master's degree in Pharmacy, Chemistry, Biotechnology, or a related scientific discipline is required, along with several years of relevant experience in pharmaceutical QC. The ability to troubleshoot analytical methods and equipment issues is also highly valued. This is a unique opportunity to contribute to healthcare advancements from a flexible remote setting, offering professional growth and the chance to work with a dedicated and quality-focused team. We are committed to upholding the highest standards of pharmaceutical quality and are seeking professionals who share this dedication.
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