1 777 Quality Control Analyst jobs in Vietnam
Pharmaceutical Quality Control Analyst
400000 Thanh Hoa , Thanh Hoa
WhatJobs
Posted 3 days ago
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Job Description
Our esteemed pharmaceutical manufacturing company is seeking a diligent and experienced Pharmaceutical Quality Control Analyst to join our dedicated QC team in Thanh Hoa, Thanh Hoa, VN . This role is critical in ensuring that our pharmaceutical products meet the highest standards of quality, safety, and efficacy, adhering to all regulatory requirements. The successful candidate will perform a wide range of laboratory tests on raw materials, in-process samples, and finished products using sophisticated analytical instrumentation and methodologies. Key responsibilities include conducting chemical and physical analyses, validating test methods, maintaining detailed laboratory records, troubleshooting equipment issues, and preparing accurate and timely reports of findings. You will be responsible for ensuring compliance with Good Manufacturing Practices (GMP) and other relevant quality standards. The ideal candidate will possess a Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific discipline, with a minimum of 2-3 years of relevant experience in a pharmaceutical QC laboratory. Strong knowledge of analytical techniques such as HPLC, GC, UV-Vis spectroscopy, and wet chemistry methods is essential. Excellent attention to detail, strong analytical and problem-solving skills, and the ability to work independently as well as collaboratively within a team are required. Proficiency in laboratory information management systems (LIMS) and relevant regulatory guidelines is a plus. We are looking for a meticulous and responsible individual who is committed to upholding product quality and patient safety. This is an excellent opportunity to contribute to the pharmaceutical industry and grow your career in a quality-focused environment. A proactive approach to identifying potential quality issues and contributing to continuous improvement initiatives is highly valued.
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0
Pharmaceutical Quality Control Analyst
65000 Nha Trang, Khanh Hoa
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Posted 7 days ago
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Job Description
Our client, a leading pharmaceutical company based in **Nha Trang, Khanh Hoa, VN**, is seeking a meticulous and detail-oriented Pharmaceutical Quality Control Analyst to join their dedicated team. This role is crucial in ensuring the safety, efficacy, and quality of our pharmaceutical products through rigorous testing and analysis. You will work within state-of-the-art laboratory facilities, contributing to the development and manufacturing of life-changing medications. We are looking for professionals with a strong scientific background and a commitment to upholding the highest quality standards.
Responsibilities:
Responsibilities:
- Perform a variety of analytical tests on raw materials, in-process samples, and finished pharmaceutical products using established methods and instrumentation.
- Operate and maintain laboratory equipment such as HPLC, GC, UV-Vis spectrophotometers, and dissolution apparatus.
- Accurately document all test results, observations, and deviations in accordance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
- Investigate and troubleshoot out-of-specification (OOS) results and deviations, collaborating with relevant departments to determine root causes.
- Prepare analytical methods and validation protocols.
- Contribute to method validation and transfer activities.
- Review and approve analytical data and reports generated by QC personnel.
- Maintain laboratory inventory and ensure availability of necessary reagents and supplies.
- Participate in internal and external audits and inspections.
- Stay current with relevant pharmacopeial standards (e.g., USP, EP) and regulatory guidelines.
- Assist in the development and implementation of new analytical methods.
- Contribute to continuous improvement initiatives within the QC department.
- Ensure a safe working environment by adhering to all safety protocols and procedures.
- Calibrate and qualify laboratory instruments as per established schedules.
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biochemistry, or a related scientific discipline.
- Minimum of 2-4 years of experience in pharmaceutical quality control or analytical testing.
- Hands-on experience with common analytical techniques and instrumentation (HPLC, GC are essential).
- Solid understanding of GMP, GLP, and regulatory requirements in the pharmaceutical industry.
- Strong analytical and problem-solving skills with keen attention to detail.
- Excellent record-keeping and documentation skills.
- Ability to work effectively in a team environment and independently.
- Proficiency in using laboratory information management systems (LIMS) is a plus.
- Good written and verbal communication skills.
- Familiarity with pharmacopeias (USP, EP) is required.
This advertiser has chosen not to accept applicants from your region.
1
Pharmaceutical Quality Control Analyst
63000 Hoi An
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Posted 8 days ago
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Job Description
Our client is seeking a meticulous and experienced Pharmaceutical Quality Control Analyst to join their state-of-the-art facility in Buon Ma Thuot, Dak Lak, VN . This critical role involves ensuring the quality and safety of pharmaceutical products through rigorous testing and analysis. The ideal candidate will possess a strong background in analytical chemistry, pharmaceuticals, and quality assurance principles, coupled with hands-on experience in a laboratory setting. You will be responsible for performing a variety of tests on raw materials, in-process samples, and finished products, meticulously documenting results, and ensuring compliance with all relevant regulatory standards, including GMP (Good Manufacturing Practices).
Key Responsibilities:
Key Responsibilities:
- Perform analytical testing on raw materials, intermediates, and finished pharmaceutical products using various laboratory techniques such as HPLC, GC, UV-Vis spectroscopy, and titration.
- Calibrate and maintain laboratory equipment to ensure accuracy and reliability of test results.
- Document all testing procedures, results, and observations in accordance with GMP guidelines and company SOPs.
- Analyze test data, prepare comprehensive reports, and communicate findings to relevant departments.
- Identify and investigate out-of-specification (OOS) results, deviations, and non-conformances, and participate in root cause analysis.
- Ensure compliance with all safety regulations and good laboratory practices (GLP).
- Assist in the validation of analytical methods and the qualification of laboratory equipment.
- Maintain inventory of laboratory supplies and reagents.
- Participate in internal and external audits as required.
- Contribute to continuous improvement initiatives within the Quality Control department.
- Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific discipline.
- Minimum of 4 years of experience in pharmaceutical quality control or a related laboratory role.
- Proficiency in operating and maintaining common analytical instruments (HPLC, GC, spectrophotometers).
- Thorough understanding of GMP, GLP, and other relevant pharmaceutical quality standards.
- Excellent analytical and problem-solving skills with meticulous attention to detail.
- Strong documentation and report-writing abilities.
- Ability to work independently and collaboratively in a fast-paced laboratory environment.
- Good understanding of Vietnamese pharmaceutical regulations is a plus.
- Proficiency in English for technical documentation and communication.
This advertiser has chosen not to accept applicants from your region.
2
Pharmaceutical Quality Control Analyst
700000 Vung Tau
WhatJobs
Posted 8 days ago
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Job Description
Our client, a leading pharmaceutical company, is seeking a meticulous and skilled Pharmaceutical Quality Control Analyst to join their team. This is a fully remote position, offering a unique opportunity for experienced professionals to contribute to critical quality assurance processes from the comfort of their home office. The role, while conceptually located in Ho Chi Minh City, Ho Chi Minh, VN , does not require physical presence and is designed for remote operation. You will be responsible for performing laboratory analyses, ensuring that raw materials, in-process samples, and finished products meet stringent quality standards and regulatory requirements.
Key Responsibilities:
Qualifications:
This is an exceptional opportunity for a skilled analyst to contribute to the development and manufacturing of life-saving medicines in a flexible remote environment.
Key Responsibilities:
- Conduct analytical testing of raw materials, intermediates, and finished pharmaceutical products using various laboratory techniques (e.g., HPLC, GC, spectroscopy).
- Analyze test results and prepare accurate and comprehensive reports.
- Ensure all testing is performed in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
- Calibrate and maintain laboratory equipment, ensuring its proper functioning.
- Validate analytical methods and document validation studies.
- Troubleshoot analytical issues and investigate out-of-specification (OOS) results.
- Maintain detailed records of all laboratory activities, including sample tracking and results.
- Participate in the development and implementation of new analytical methods.
- Collaborate with R&D, manufacturing, and regulatory affairs teams.
- Review and approve quality control documentation, such as Certificates of Analysis (CoAs).
- Stay up-to-date with scientific advancements and regulatory changes in the pharmaceutical industry.
- Contribute to internal audits and inspections.
- Assist in the qualification of new laboratory equipment and suppliers.
- Ensure a safe working environment by adhering to all safety protocols.
- Manage time effectively to meet testing deadlines and project timelines.
Qualifications:
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related science field.
- Minimum of 3 years of experience in pharmaceutical quality control or analytical testing.
- Hands-on experience with analytical instrumentation such as HPLC, GC, UV-Vis, IR, etc.
- Strong understanding of pharmaceutical quality systems, GMP, and GLP.
- Proficiency in data analysis and interpretation.
- Excellent documentation and record-keeping skills.
- Strong problem-solving and critical thinking abilities.
- Ability to work independently with minimal supervision in a remote setting.
- Effective communication and interpersonal skills.
- Detail-oriented with a high level of accuracy.
- Familiarity with pharmacopeias (e.g., USP, EP) is desirable.
- Experience with method validation and OOS investigations is a plus.
- Proficiency in relevant software (e.g., LIMS, MS Office).
- Commitment to quality and patient safety.
- Ability to manage multiple tasks and prioritize effectively.
This is an exceptional opportunity for a skilled analyst to contribute to the development and manufacturing of life-saving medicines in a flexible remote environment.
This advertiser has chosen not to accept applicants from your region.
3
Pharmaceutical Quality Control Analyst
50000 Vung Tau
WhatJobs
Posted 8 days ago
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Job Description
Our client is seeking a meticulous and knowledgeable Pharmaceutical Quality Control Analyst to join their dedicated team. This role is crucial for ensuring that all pharmaceutical products meet stringent quality standards and regulatory requirements. You will be responsible for conducting a range of laboratory tests, analyzing data, and documenting findings to uphold product integrity. The ideal candidate will possess a strong background in analytical chemistry, familiarity with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP), and experience with various analytical instruments.
Key Responsibilities:
This position offers a hybrid work model, providing a blend of on-site laboratory work in Vung Tau, Ba Ria–Vung Tau, VN and remote responsibilities such as data analysis and report generation. You will collaborate closely with the Quality Assurance team and production staff to maintain the highest levels of product quality. Strong analytical, problem-solving, and communication skills are essential.
Key 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, titration).
- Analyze test results and compare them against established specifications.
- Document all testing procedures, results, and deviations accurately in laboratory notebooks and electronic systems.
- Prepare and standardize reagents and solutions.
- Maintain and calibrate laboratory equipment.
- Identify and report any out-of-specification (OOS) results and assist in investigations.
- Participate in method validation and verification activities.
- Ensure compliance with all safety regulations and laboratory procedures.
- Contribute to continuous improvement initiatives within the quality control department.
- Review and approve batch records and quality control documentation.
This position offers a hybrid work model, providing a blend of on-site laboratory work in Vung Tau, Ba Ria–Vung Tau, VN and remote responsibilities such as data analysis and report generation. You will collaborate closely with the Quality Assurance team and production staff to maintain the highest levels of product quality. Strong analytical, problem-solving, and communication skills are essential.
This advertiser has chosen not to accept applicants from your region.
4
Pharmaceutical Quality Control Analyst
10000 An Cu, An Giang
WhatJobs
Posted 8 days ago
Job Viewed
Job Description
Our client is seeking a diligent and detail-oriented Pharmaceutical Quality Control Analyst to join their state-of-the-art facility in **Hanoi, Hanoi, VN**. This critical role involves performing a wide range of tests and analyses to ensure the quality, safety, and efficacy of pharmaceutical products. The ideal candidate possesses a strong background in chemistry or a related science, extensive experience with analytical instrumentation, and a thorough understanding of GMP and regulatory guidelines within the pharmaceutical industry.
Key Responsibilities:
Key Responsibilities:
- Conduct various analytical tests on raw materials, in-process samples, and finished products using techniques such as HPLC, GC, UV-Vis spectroscopy, and titration.
- Perform method validation and transfer studies as required.
- Prepare and standardize reagents and solutions necessary for testing.
- Maintain laboratory equipment, ensuring proper calibration, operation, and maintenance.
- Document all laboratory activities, test results, and observations accurately and meticulously in accordance with GMP and company SOPs.
- Investigate out-of-specification (OOS) results and deviations, identifying root causes and recommending corrective actions.
- Participate in internal and external audits, providing necessary documentation and explanations.
- Stay current with pharmacopeial standards (e.g., USP, EP, JP) and relevant regulatory guidelines.
- Collaborate with R&D, production, and regulatory affairs departments to resolve quality issues.
- Contribute to the continuous improvement of quality control processes and laboratory efficiency.
- Ensure compliance with all safety regulations and maintain a clean and organized laboratory environment.
- Assist in the development and implementation of new analytical methods.
- Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, Biochemistry, or a related field.
- Minimum of 3 years of hands-on experience in a pharmaceutical quality control laboratory setting.
- Proficiency with analytical instrumentation, particularly HPLC and GC.
- Strong understanding of Good Manufacturing Practices (GMP) and regulatory requirements for pharmaceuticals.
- Excellent laboratory techniques, documentation skills, and attention to detail.
- Ability to work independently and as part of a team in a fast-paced environment.
- Strong problem-solving and analytical skills.
- Good written and verbal communication skills.
- Experience with stability studies is a plus.
- Familiarity with laboratory information management systems (LIMS) is an advantage.
This advertiser has chosen not to accept applicants from your region.
5
Pharmaceutical Quality Control Analyst
100000 An Cu, An Giang
WhatJobs
Posted 8 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is seeking a meticulous and dedicated Pharmaceutical Quality Control Analyst to join their state-of-the-art laboratory in **Hanoi, Hanoi, VN**. This on-site role is crucial for ensuring the quality, safety, and efficacy of pharmaceutical products. You will perform a variety of analytical tests on raw materials, in-process samples, and finished products using advanced laboratory equipment and techniques. Responsibilities include executing analytical methods, documenting results accurately, maintaining laboratory equipment, adhering to Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP), and investigating any deviations or out-of-specification (OOS) results. The ideal candidate will possess a Bachelor's or Master's degree in Chemistry, Pharmacy, Biotechnology, or a related scientific discipline. A minimum of 3-5 years of experience in pharmaceutical quality control is required, with hands-on experience in techniques such as HPLC, GC, spectroscopy (UV-Vis, IR), and dissolution testing. Strong understanding of pharmacopeial standards (e.g., USP, EP) and regulatory requirements is essential. You must have excellent attention to detail, strong analytical and problem-solving skills, and the ability to work both independently and as part of a team. Proficiency in data analysis and reporting is a must. This role offers a fantastic opportunity to contribute to the development and production of life-saving medications within a dynamic and growing industry. Join our client in **Hanoi, Hanoi, VN** and be part of a team committed to excellence in pharmaceutical quality.
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6
Pharmaceutical Quality Control Analyst
50000 Vung Tau
WhatJobs
Posted 8 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is seeking a meticulous and detail-oriented Pharmaceutical Quality Control Analyst to join their team in Vung Tau, Ba Ria–Vung Tau, VN . This hybrid role involves both laboratory analysis and documentation review to ensure the quality and safety of pharmaceutical products. The ideal candidate will have a strong background in analytical chemistry and a thorough understanding of regulatory compliance within the pharmaceutical industry.
Responsibilities:
Responsibilities:
- Perform a variety of analytical tests on raw materials, in-process samples, and finished pharmaceutical products using techniques such as HPLC, GC, UV-Vis, and titration.
- Develop, validate, and transfer analytical methods according to regulatory guidelines.
- Calibrate and maintain laboratory equipment, ensuring proper functioning and accuracy.
- Analyze and interpret test results, preparing accurate and comprehensive reports.
- Investigate out-of-specification (OOS) results and deviations, identifying root causes and implementing corrective actions.
- Ensure compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant regulatory standards.
- Review batch records and other quality documentation for completeness and accuracy.
- Participate in internal and external audits as required.
- Contribute to process improvement initiatives within the Quality Control department.
- Maintain a clean, safe, and organized laboratory environment.
- Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or a related scientific field.
- Minimum of 3 years of experience in pharmaceutical quality control or analytical testing.
- Proficiency with analytical instrumentation, particularly HPLC and GC.
- Solid understanding of GMP, GLP, and relevant pharmaceutical regulations (e.g., ICH guidelines).
- Excellent analytical and problem-solving skills.
- Strong attention to detail and accuracy.
- Good written and verbal communication skills.
- Ability to work effectively both independently and as part of a team in a hybrid environment.
- Proficiency in using laboratory information management systems (LIMS) and other relevant software.
- Commitment to maintaining a high standard of quality and compliance.
This advertiser has chosen not to accept applicants from your region.
7
Pharmaceutical Quality Control Analyst
41000 Thanh Hoa , Thanh Hoa
WhatJobs
Posted 8 days ago
Job Viewed
Job Description
Our client seeks a meticulous and skilled Pharmaceutical Quality Control Analyst to join their state-of-the-art laboratory in Thanh Hoa, Thanh Hoa, VN . This critical role ensures the quality, safety, and efficacy of pharmaceutical products through rigorous testing and analysis. You will perform a variety of chemical and physical tests on raw materials, in-process samples, and finished products, adhering strictly to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). Your responsibilities include operating and maintaining analytical equipment such as HPLC, GC, UV-Vis spectrophotometers, and titrators.
The ideal candidate will possess a strong background in chemistry, pharmacy, or a related life science field, with a minimum of 2 years of experience in pharmaceutical quality control. You must have hands-on experience with analytical instrumentation and a thorough understanding of pharmacopeial standards (e.g., USP, EP, JP). Excellent documentation skills are essential, as you will be responsible for accurately recording test results, maintaining laboratory notebooks, and preparing analytical reports. You should be adept at troubleshooting analytical methods and identifying deviations from specifications.
This position requires a keen eye for detail, a commitment to scientific integrity, and the ability to work effectively within a team. You will collaborate with R&D, production, and regulatory affairs departments to resolve quality issues and ensure compliance. Familiarity with quality management systems and regulatory submissions is a plus. The work environment is dynamic and demands adherence to strict safety protocols. This is an excellent opportunity for a dedicated professional to contribute to the development and manufacturing of high-quality pharmaceuticals in Thanh Hoa, Thanh Hoa, VN .
Key Responsibilities:
The ideal candidate will possess a strong background in chemistry, pharmacy, or a related life science field, with a minimum of 2 years of experience in pharmaceutical quality control. You must have hands-on experience with analytical instrumentation and a thorough understanding of pharmacopeial standards (e.g., USP, EP, JP). Excellent documentation skills are essential, as you will be responsible for accurately recording test results, maintaining laboratory notebooks, and preparing analytical reports. You should be adept at troubleshooting analytical methods and identifying deviations from specifications.
This position requires a keen eye for detail, a commitment to scientific integrity, and the ability to work effectively within a team. You will collaborate with R&D, production, and regulatory affairs departments to resolve quality issues and ensure compliance. Familiarity with quality management systems and regulatory submissions is a plus. The work environment is dynamic and demands adherence to strict safety protocols. This is an excellent opportunity for a dedicated professional to contribute to the development and manufacturing of high-quality pharmaceuticals in Thanh Hoa, Thanh Hoa, VN .
Key Responsibilities:
- Perform analytical testing on raw materials, intermediates, and finished pharmaceutical products.
- Operate and maintain analytical instruments (e.g., HPLC, GC, UV-Vis).
- Ensure compliance with GLP, GMP, and pharmacopeial standards.
- Document all laboratory activities and results accurately.
- Investigate out-of-specification (OOS) results and deviations.
- Prepare analytical reports and certificates of analysis.
- Collaborate with cross-functional teams on quality-related issues.
- Participate in method validation and transfer activities.
- Bachelor's degree in Chemistry, Pharmacy, Biology, or a related field.
- Minimum 2 years of experience in pharmaceutical QC/QA.
- Proficiency with analytical instrumentation and laboratory techniques.
- Strong understanding of pharmacopeias and regulatory guidelines.
- Excellent documentation and reporting skills.
- Ability to work independently and in a team environment.
- Knowledge of quality management systems.
This advertiser has chosen not to accept applicants from your region.
8
Pharmaceutical Quality Control Analyst
65000 Nha Trang, Khanh Hoa
WhatJobs
Posted 8 days ago
Job Viewed
Job Description
Our client, a reputable pharmaceutical company, is seeking a diligent and analytical Pharmaceutical Quality Control Analyst to join their team in Nha Trang, Khanh Hoa, VN . This role is pivotal in ensuring the quality, safety, and efficacy of pharmaceutical products through rigorous testing and analysis. The ideal candidate will possess a strong scientific background and meticulous attention to detail.
Key responsibilities include performing in-process and finished product testing using various analytical techniques, such as HPLC, GC, and spectroscopy; preparing and standardizing reagents and solutions; maintaining detailed and accurate laboratory records and documentation; ensuring compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP); troubleshooting and resolving analytical issues; calibrating and maintaining laboratory equipment; participating in method validation and transfer activities; assisting in the investigation of out-of-specification (OOS) results; and contributing to the continuous improvement of quality control processes.
The ideal candidate will hold a Bachelor's or Master's degree in Chemistry, Pharmacy, Biology, or a related life science field. A minimum of 3 years of experience in a pharmaceutical quality control laboratory is required. Proven experience with analytical instrumentation (HPLC, GC, UV-Vis, etc.) is essential. Strong understanding of pharmaceutical regulations and quality systems is a must. Excellent analytical, problem-solving, and organizational skills are crucial. The ability to work effectively in a team environment and communicate scientific findings clearly is also important. This role offers a hybrid work arrangement, balancing laboratory-based analysis with documentation and reporting that can be completed remotely.
This hybrid role requires a presence in our client's state-of-the-art laboratory facilities in Nha Trang for essential hands-on testing and analysis, with flexibility for remote work on data analysis, report writing, and other documentation tasks. Our client provides a stimulating work environment with opportunities for professional growth and development in the pharmaceutical industry.
Key responsibilities include performing in-process and finished product testing using various analytical techniques, such as HPLC, GC, and spectroscopy; preparing and standardizing reagents and solutions; maintaining detailed and accurate laboratory records and documentation; ensuring compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP); troubleshooting and resolving analytical issues; calibrating and maintaining laboratory equipment; participating in method validation and transfer activities; assisting in the investigation of out-of-specification (OOS) results; and contributing to the continuous improvement of quality control processes.
The ideal candidate will hold a Bachelor's or Master's degree in Chemistry, Pharmacy, Biology, or a related life science field. A minimum of 3 years of experience in a pharmaceutical quality control laboratory is required. Proven experience with analytical instrumentation (HPLC, GC, UV-Vis, etc.) is essential. Strong understanding of pharmaceutical regulations and quality systems is a must. Excellent analytical, problem-solving, and organizational skills are crucial. The ability to work effectively in a team environment and communicate scientific findings clearly is also important. This role offers a hybrid work arrangement, balancing laboratory-based analysis with documentation and reporting that can be completed remotely.
This hybrid role requires a presence in our client's state-of-the-art laboratory facilities in Nha Trang for essential hands-on testing and analysis, with flexibility for remote work on data analysis, report writing, and other documentation tasks. Our client provides a stimulating work environment with opportunities for professional growth and development in the pharmaceutical industry.
This advertiser has chosen not to accept applicants from your region.
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