444 Quality Analyst jobs in Vietnam

Thoughtworks is expanding to Vietnam and we're looking for passionate technologists to be part of the pioneering team with direct support from our Southeast Asia team in Singapore and Thailand. This is an exciting time to join us at our new Ho Chi Minh City office, where you will be based in Dreamplex Tran Quang Khai at 62 Trần Quang Khải, Tân Định, Quận 1.

Woven between all the stages of the delivery process is the work of a Quality Analyst: the technologist who focuses on the complexity and risk inherent in building solutions. By collaborating with each team member—Developer, Business Analyst, Designer, etc.—they ensure quality is thoughtfully examined in both processes and technology. QAs are more than testers; they're team motivators and strive to inspire all teammates to weave quality into their mindsets and code.

**Job responsibilities**:

- Aim to shift quality to the left in alignment with senior client stakeholders
- Partner with senior stakeholders to understand the product, create a quality strategy and ensure that the teams are empowered to implement it
- Highlight risks to software delivery and assist in managing them alongside the leadership team
- Regularly carry out exploratory testing to gain insights and uncover potential risks
- Drive improvements for clean code, tests, testability and advice on test tools/frameworks
- Define, discuss and implement a program approach to testing across multiple products/services and domains, commonly referred to as "UAT", "E2E", etc.
- Influence a consistent approach in automation of tests across teams in a program, e.g. nomenclature, domain boundaries, contracts between services, distinct layers, common tooling and dashboard representations in the right situation
- You will be nimble and alter your team's approach based on an industry's standards and regulations
- Coach team members across roles to help deliver better quality software and help them adopt a testing mindset
- Advocate QA expertise to the tech community inside Thoughtworks and throughout the broader industry, speaking at conferences and acting as a mentor for junior-level QAs

**Job qualifications**:
**Technical skills**:

- You have worked as a Quality Analyst as part of a wider development team, pairing with Devs, Business Analysts, Infrastructure Engineers, and Designers to embed quality and testing mindsets within different roles
- You are comfortable with agile, code management, deployment strategies, migration strategies and release management
- You have extensive experience with practices such as TDD, BDD, CI/CD and models such as Test Pyramid and Swiss cheese
- Can drive changes to both on premise and cloud architectures for enhancing quality
- Strategize different types of functional and cross-functional testing including performance and security testing across various architectures and domain models
- You can leverage metrics in order to make improvement to lead time, deployment frequency, mean time to recovery and change fail rate
- You can design quality strategies and can produce one for large programs

**Professional skills**:

- You enjoy influencing teammates and senior leaders and advocating for quality as a shared team responsibility
- Knowledge of user experience and user research including prototyping, personas and AB testing, which can be translated into a test strategy
- You are passionate about ensuring the correct product is being built, not just that it is being built correctly.
- You are a natural leader who can foster effective and inclusive teams that deliver
- You thrive in safe, collaborative environments where different opinions, ideas and perspectives are freely shared

**Other things to know**:
**L&D**:
There is no one-size-fits-all career path at Thoughtworks: however you want to develop your career is entirely up to you. But we also balance autonomy with the strength of our cultivation culture. This means your career is supported by interactive tools, numerous development programs and teammates who want to help you grow. We see value in helping each other be our best and that extends to empowering our employees in their career journeys.

**About Thoughtworks**:
Thoughtworks is a global technology consultancy that integrates strategy, design and engineering to drive digital innovation. For 28+ years, our clients have trusted our autonomous teams to build solutions that look past the obvious. Here, computer science grads come together with seasoned technologists, self-taught developers, midlife career changers and more to learn from and challenge each other. Career journeys flourish with the strength of our cultivation culture, which has won numerous awards around the world.

Join Thoughtworks and thrive. Together, our extra curiosity, innovation, passion and dedication overcomes ordinary.

LI-SEA

Our client is seeking a meticulous and dedicated Pharmaceutical Quality Control Analyst to join their laboratory team in Buon Ma Thuot, Dak Lak, VN . This hybrid role requires a professional with a strong understanding of pharmaceutical manufacturing processes and quality assurance principles. You will be responsible for performing a variety of analytical tests on raw materials, in-process samples, and finished products to ensure they meet stringent quality and regulatory standards. Your duties will include operating and maintaining laboratory equipment, preparing reagents and samples, and accurately recording test results. The ideal candidate will possess a Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field. Previous experience in a pharmaceutical QC laboratory setting is highly desirable. Proficiency in analytical techniques such as HPLC, GC, spectroscopy, and wet chemistry methods is essential. You should have a keen eye for detail, strong organizational skills, and the ability to follow standard operating procedures (SOPs) meticulously. Familiarity with Good Laboratory Practices (GLP) and regulatory guidelines (e.g., GMP) is crucial. This role involves precise execution of tests, accurate data recording, and contributing to the overall quality assurance of pharmaceutical products. You will work collaboratively with other members of the QC team and interact with production and regulatory affairs departments. The ability to troubleshoot equipment issues and identify deviations from expected results is also important. Your commitment to quality and accuracy will be vital in ensuring the safety and efficacy of the medicines produced. You will play a key role in maintaining compliance and upholding the company's reputation for quality.

Responsibilities:

• Perform analytical testing on raw materials, intermediates, and finished products.
• Operate and maintain laboratory equipment (HPLC, GC, UV-Vis, IR, etc.).
• Prepare reagents, standards, and samples for testing.
• Follow and adhere to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
• Accurately record and report test results.
• Assist in the investigation of out-of-specification (OOS) results.
• Prepare certificates of analysis (CoA).
• Maintain laboratory cleanliness and organization.
• Participate in method validation and transfer activities.
• Ensure compliance with all relevant quality and regulatory guidelines.

Qualifications:

• Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific discipline.
• 2+ years of experience in pharmaceutical quality control or a similar laboratory role.
• Proficiency in analytical techniques (HPLC, GC, spectroscopy, titrations).
• Knowledge of pharmaceutical regulations (GMP, GLP).
• Strong attention to detail and accuracy.
• Excellent record-keeping and documentation skills.
• Ability to work independently and as part of a team.
• Good understanding of laboratory safety procedures.

Our client, a leading pharmaceutical company, is seeking a meticulous and highly skilled Pharmaceutical Quality Control Analyst to join their esteemed quality assurance team. This vital role ensures that all pharmaceutical products meet stringent quality standards and regulatory requirements before release. You will perform a variety of laboratory tests on raw materials, in-process samples, and finished products using advanced analytical techniques and equipment. Key responsibilities include executing test methods, documenting results accurately, maintaining laboratory equipment, and adhering to Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP). The ideal candidate will have a strong background in chemistry, analytical science, or a related field, coupled with hands-on experience in pharmaceutical quality control. Proficiency with analytical instrumentation such as HPLC, GC, UV-Vis spectrophotometry, and dissolution testers is essential. You should possess excellent attention to detail, meticulous record-keeping skills, and a deep understanding of pharmaceutical regulations and quality systems. This role requires a commitment to accuracy, safety, and scientific integrity. You will play a critical part in ensuring the safety and efficacy of our client's pharmaceutical products. We are looking for a team player who can collaborate effectively with research and development, production, and regulatory affairs departments. This position offers an excellent opportunity for professional growth within the pharmaceutical industry, contributing to the development of life-saving medications. Your dedication to quality will directly impact patient well-being. The ability to troubleshoot analytical methods and participate in method validation activities is highly valued.

Responsibilities:

• Perform analytical tests on raw materials, intermediates, and finished pharmaceutical products.
• Execute test methods accurately using various laboratory equipment (e.g., HPLC, GC, UV-Vis, dissolution apparatus).
• Document all testing procedures and results in compliance with GMP and GLP guidelines.
• Calibrate and maintain laboratory instruments to ensure proper functioning.
• Prepare reagents and standards required for testing.
• Investigate out-of-specification (OOS) or out-of-trend (OOT) results.
• Participate in method validation and transfer activities.
• Ensure compliance with all safety regulations and laboratory procedures.
• Review and approve analytical data generated by other team members.
• Contribute to the continuous improvement of quality control processes.

Qualifications:

• Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, Biotechnology, or a related scientific field.
• Minimum of 2-4 years of experience in pharmaceutical quality control or a related analytical laboratory setting.
• Proven experience with analytical instrumentation (HPLC, GC, UV-Vis, FTIR, etc.).
• Strong understanding of GMP, GLP, and regulatory requirements (e.g., FDA, EMA).
• Excellent analytical skills and attention to detail.
• Proficiency in laboratory documentation and data management.
• Ability to work independently and as part of a team.
• Good problem-solving skills and a methodical approach.
• Strong written and verbal communication skills.
• Familiarity with pharmacopeial methods (USP, EP) is a plus.

This role is based in the vibrant city of Da Nang, Da Nang, VN , contributing to the advancement of healthcare.

Our client is seeking a meticulous and experienced Pharmaceutical Quality Control Analyst to join their dedicated team in Vung Tau, Ba Ria–Vung Tau, VN . This vital role ensures the quality and safety of pharmaceutical products by performing rigorous testing and analysis. You will be responsible for conducting in-process and finished product testing, utilizing a variety of analytical techniques and laboratory equipment. Key responsibilities include performing assays, dissolution testing, impurity profiling, and stability studies according to established protocols and Good Manufacturing Practices (GMP). The ideal candidate will have a strong background in analytical chemistry, instrumental analysis (HPLC, GC, UV-Vis, IR), and wet chemistry techniques. You will be required to meticulously document all testing procedures, results, and deviations in compliance with regulatory standards. This position requires a keen eye for detail, excellent laboratory skills, and the ability to interpret complex data. The Pharmaceutical Quality Control Analyst will collaborate with R&D, production, and regulatory affairs departments to address quality-related issues. You will also participate in method validation and instrument calibration activities. Accurate record-keeping and adherence to safety protocols are paramount. This role is laboratory-based, demanding precision and commitment to quality in the Vung Tau, Ba Ria–Vung Tau, VN facility. A Bachelor's degree in Chemistry, Pharmacy, or a related life science field, along with a minimum of 3 years of experience in pharmaceutical quality control, is required. Experience with specific pharmacopoeias (e.g., USP, EP) is highly beneficial.

Our client, a leading pharmaceutical company, is looking for a meticulous and experienced Pharmaceutical Quality Control Analyst to join their team in Thai Binh, Thai Binh, VN . This role is critical in ensuring the quality and safety of pharmaceutical products by performing rigorous testing and analysis. The successful candidate will work in a state-of-the-art laboratory environment, adhering to strict regulatory standards and contributing to the overall quality assurance of manufactured drugs.

Key Responsibilities:

• Perform in-process and finished product testing using various analytical techniques, including HPLC, GC, UV-Vis, and titration.
• Analyze raw materials, intermediates, and final products to ensure they meet established specifications and quality standards.
• Prepare and standardize reagents and solutions required for laboratory analysis.
• Maintain accurate and detailed laboratory records, including test results, procedures, and deviations, in compliance with GMP guidelines.
• Calibrate and maintain laboratory equipment, ensuring its proper functioning and performance.
• Troubleshoot analytical methods and instrumentation when necessary.
• Review and interpret analytical data, identify out-of-specification (OOS) results, and participate in investigations.
• Write and revise Standard Operating Procedures (SOPs) for laboratory testing and equipment operation.
• Participate in method validation and transfer activities.
• Ensure a safe working environment by adhering to all safety protocols and handling chemicals appropriately.
• Collaborate with other departments, such as Production, Research & Development, and Quality Assurance, to resolve quality issues.
• Prepare reports on testing activities and analytical findings.
• Stay updated with regulatory requirements and industry best practices in pharmaceutical quality control.
  
  Qualifications:
  
  • Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
  • Minimum of 2-4 years of experience in pharmaceutical quality control or a related laboratory setting.
  • Hands-on experience with analytical instrumentation common in pharmaceutical QC labs (HPLC, GC, etc.).
  • Strong knowledge of Good Manufacturing Practices (GMP), pharmacopeial standards (USP, EP), and regulatory guidelines.
  • Excellent laboratory technique, analytical skills, and attention to detail.
  • Proficiency in data analysis and interpretation.
  • Strong written and verbal communication skills in Vietnamese and English.
  • Ability to work independently and as part of a team in a fast-paced environment.
  • Good record-keeping and documentation skills.
  • Familiarity with laboratory information management systems (LIMS) is a plus.
  
  This is an on-site position located in Thai Binh, Thai Binh, VN . We are looking for a dedicated professional who is committed to upholding the highest standards of quality and safety in pharmaceutical manufacturing. If you possess the required skills and experience, we encourage you to apply.

A leading pharmaceutical company is seeking a meticulous and dedicated Pharmaceutical Quality Control Analyst to join their team in Da Nang, Da Nang, VN . This on-site role is critical to ensuring the quality, safety, and efficacy of our pharmaceutical products. You will be responsible for performing a variety of laboratory tests and analyses on raw materials, in-process samples, and finished products to ensure they meet strict quality standards and regulatory requirements. The ideal candidate will possess a strong background in analytical chemistry or a related scientific discipline, along with hands-on experience with laboratory equipment and testing methodologies. You will work under Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) guidelines. Key responsibilities include executing test methods, documenting results accurately, troubleshooting analytical procedures, and participating in method validation activities. You will also be involved in maintaining laboratory equipment, ensuring proper calibration, and contributing to the continuous improvement of quality control processes. We are looking for an individual with exceptional attention to detail, strong problem-solving skills, and a commitment to scientific integrity. Your ability to work independently and as part of a team, along with excellent data recording and reporting skills, will be essential for success. Join a company that is committed to improving health outcomes and offers a stimulating work environment with opportunities for professional development.

Key Responsibilities:

• Performing analytical tests on pharmaceutical products using various laboratory techniques.
• Ensuring compliance with GMP and GLP standards.
• Documenting all testing procedures and results accurately.
• Calibrating and maintaining laboratory equipment.
• Troubleshooting analytical methods and identifying root causes of deviations.
• Preparing reports on test results and quality assessments.
• Participating in method validation and transfer activities.
• Collaborating with R&D and production teams to address quality issues.

Qualifications:

• Bachelor's or Master's degree in Chemistry, Pharmacy, or a related science field.
• 2+ years of experience in pharmaceutical quality control or a related laboratory setting.
• Proficiency in analytical techniques such as HPLC, GC, UV-Vis, and titration.
• Knowledge of pharmaceutical regulations (e.g., FDA, ICH).
• Strong attention to detail and accuracy.
• Excellent record-keeping and documentation skills.
• Ability to work independently and in a team environment.

Our client, a rapidly growing pharmaceutical company, is seeking a meticulous and detail-oriented Pharmaceutical Quality Control Analyst to join their team in Buon Ma Thuot, Dak Lak, VN . This position offers a hybrid work model, combining essential laboratory work with remote data analysis and reporting.

The Pharmaceutical Quality Control Analyst will be responsible for performing a wide range of laboratory tests and analyses to ensure the quality, safety, and efficacy of pharmaceutical products. You will play a crucial role in maintaining compliance with regulatory standards and contributing to the overall success of our client's product development and manufacturing processes.

Key Responsibilities:

• Conduct analytical testing of raw materials, in-process samples, and finished products using various laboratory techniques (e.g., HPLC, GC, spectroscopy, titration).
• Prepare reagents, calibrate instruments, and maintain laboratory equipment to ensure accuracy and reliability.
• Analyze test results, interpret data, and prepare detailed reports documenting findings.
• Identify and investigate any deviations from established specifications or procedures.
• Ensure all activities are performed in compliance with Good Manufacturing Practices (GMP) and other relevant regulatory guidelines.
• Maintain accurate and organized laboratory records, batch records, and testing documentation.
• Participate in method validation and transfer activities.
• Collaborate with R&D, production, and regulatory affairs departments to resolve quality issues.
• Stay current with scientific advancements and regulatory changes in the pharmaceutical industry.

Qualifications:

• Bachelor's or Master's degree in Chemistry, Pharmacy, Biotechnology, or a related scientific field.
• Minimum of 3 years of experience in pharmaceutical quality control or a similar laboratory environment.
• Hands-on experience with analytical instrumentation (e.g., HPLC, GC, UV-Vis, FTIR).
• Strong understanding of GMP, ICH guidelines, and pharmaceutical quality systems.
• Excellent analytical, problem-solving, and critical-thinking skills.
• Proficiency in data analysis and scientific report writing.
• Strong attention to detail and accuracy.
• Good laboratory practices (GLP) and safety awareness.
• Effective communication and teamwork skills.

This role offers a challenging and rewarding opportunity to contribute to the development of life-saving medicines and grow your career in the pharmaceutical sector.

Our client, a leading pharmaceutical company, is seeking a meticulous and experienced Pharmaceutical Quality Control Analyst. This role is crucial for ensuring the quality and safety of pharmaceutical products. Located in **Long Xuyen, An Giang, VN**, this position offers a hybrid work arrangement, balancing essential lab work with remote data analysis and reporting. You will perform a variety of laboratory tests on raw materials, in-process samples, and finished products to ensure they meet stringent quality standards and regulatory requirements.

Key Responsibilities:

• Perform analytical testing on raw materials, intermediates, and finished pharmaceutical products using various techniques such as HPLC, GC, UV-Vis spectroscopy, and wet chemistry.
• Prepare reagents, standards, and samples for testing according to approved procedures.
• Calibrate and maintain laboratory equipment, ensuring proper functioning and accuracy.
• Accurately record and document all testing results in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
• Analyze test data, interpret results, and prepare reports summarizing findings.
• Investigate out-of-specification (OOS) or out-of-trend (OOT) results and contribute to deviation investigations.
• Participate in method validation and transfer activities.
• Ensure all laboratory activities are conducted in compliance with company policies, SOPs, and regulatory guidelines (e.g., FDA, WHO).
• Maintain a clean and organized laboratory environment.
• Stay updated on scientific advancements and relevant industry regulations.
• Collaborate with R&D, production, and quality assurance departments to resolve quality issues.
• Assist in the development and optimization of analytical methods.
• Prepare and maintain inventory of laboratory supplies and chemicals.
• Conduct stability studies and analyze the resulting data.
• Contribute to internal audits and regulatory inspections.

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 a similar laboratory setting.
• Strong knowledge and hands-on experience with analytical instruments like HPLC, GC, FTIR, and UV-Vis spectrophotometers.
• Familiarity with pharmacopeial methods (e.g., USP, EP, JP).
• Understanding of GMP, GLP, and other relevant regulatory guidelines.
• Excellent data analysis and interpretation skills.
• Proficiency in using laboratory information management systems (LIMS) and Microsoft Office Suite.
• Strong attention to detail and accuracy in record-keeping.
• Good written and verbal communication skills.
• Ability to work effectively both independently and as part of a team in a hybrid work environment.
• Problem-solving abilities and a methodical approach to tasks.
• Experience with method validation and troubleshooting analytical equipment is a plus.

This is a vital role in maintaining the high standards of our pharmaceutical products. Join us in **Long Xuyen, An Giang, VN** and contribute to public health.

Our client is seeking a meticulous and experienced Pharmaceutical Quality Control Analyst to join their team in a fully remote capacity. This role is critical in ensuring the quality, safety, and efficacy of pharmaceutical products by performing rigorous analytical testing and adhering to strict regulatory guidelines. You will be responsible for conducting a range of tests on raw materials, in-process samples, and finished products using various laboratory techniques and instruments. The ideal candidate will possess a strong foundation in analytical chemistry, a thorough understanding of GMP (Good Manufacturing Practices), and experience with pharmaceutical quality control procedures. Your responsibilities will include preparing samples, operating and calibrating analytical equipment (e.g., HPLC, GC, UV-Vis spectrophotometers), interpreting test results, documenting findings accurately, and troubleshooting analytical methods. You will also play a key role in ensuring that all laboratory activities comply with FDA, EMA, and other relevant regulatory standards. This remote position requires exceptional attention to detail, strong organizational skills, and the ability to work independently while maintaining high-quality standards. You will collaborate with R&D teams and manufacturing personnel to resolve quality issues and contribute to process improvements. A commitment to maintaining the integrity of the pharmaceutical supply chain is paramount. Responsibilities:

• Perform analytical testing on raw materials, intermediates, and finished pharmaceutical products using various laboratory techniques.
• Operate, calibrate, and maintain analytical instruments such as HPLC, GC, UV-Vis, FTIR, and dissolution testers.
• Prepare reagents, standards, and samples according to established protocols.
• Interpret test results, compare them against specifications, and document findings accurately in lab notebooks and reports.
• Troubleshoot analytical methods and instrumentation as needed.
• Ensure compliance with all applicable regulatory guidelines, including GMP, ICH, and USP.
• Maintain a clean and organized laboratory environment.
• Participate in method validation and transfer activities.
• Collaborate with cross-functional teams (R&D, Manufacturing) to address quality-related issues.
• Contribute to the continuous improvement of quality control processes and procedures.

Qualifications:

• Bachelor's or Master's degree in Chemistry, Pharmacy, Biochemistry, or a related scientific field.
• Minimum of 3-5 years of experience in pharmaceutical quality control or analytical laboratory testing.
• Hands-on experience with analytical instrumentation (HPLC, GC, UV-Vis are essential).
• Strong knowledge of GMP, ICH guidelines, and pharmacopeial standards (USP, EP).
• Proficiency in data analysis and interpretation, with excellent documentation skills.
• Excellent problem-solving abilities and attention to detail.
• Ability to work independently and manage time effectively in a remote setting.
• Strong written and verbal communication skills.
• Familiarity with electronic laboratory notebooks (ELN) and laboratory information management systems (LIMS) is a plus.

This remote role offers a vital contribution to pharmaceutical product quality.