135 Quality Control Analyst jobs in Vietnam
Pharmaceutical Quality Control Analyst
630000 Hoi An
WhatJobs
Posted today
Job Viewed
Job Description
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:
Qualifications:
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.
This advertiser has chosen not to accept applicants from your region.
0
Pharmaceutical Quality Control Analyst
550000 Hoa Sơn
WhatJobs
Posted today
Job Viewed
Job Description
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:
Qualifications:
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 advertiser has chosen not to accept applicants from your region.
1
Pharmaceutical Quality Control Analyst
51000 An Thanh
WhatJobs
Posted today
Job Viewed
Job Description
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.
This advertiser has chosen not to accept applicants from your region.
2
Pharmaceutical Quality Control Analyst
370000 Thai Binh , Thai Binh
WhatJobs
Posted today
Job Viewed
Job Description
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:
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.
This advertiser has chosen not to accept applicants from your region.
3
Pharmaceutical Quality Control Analyst
550000 Hoa Sơn
WhatJobs
Posted today
Job Viewed
Job Description
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:
Qualifications:
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.
This advertiser has chosen not to accept applicants from your region.
4
Pharmaceutical Quality Control Analyst
63000 Hoi An
WhatJobs
Posted today
Job Viewed
Job Description
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:
Qualifications:
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.
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.
This advertiser has chosen not to accept applicants from your region.
5
Pharmaceutical Quality Control Analyst
91000 Long Xuyen, An Giang
WhatJobs
Posted today
Job Viewed
Job Description
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:
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.
- 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 advertiser has chosen not to accept applicants from your region.
Be The First To Know
About the latest Quality control analyst Jobs in Vietnam !
6
Pharmaceutical Quality Control Analyst
55000 Hoa Sơn
WhatJobs
Posted today
Job Viewed
Job Description
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.
- 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 advertiser has chosen not to accept applicants from your region.
7
Pharmaceutical Quality Control Analyst
60000 Pleiku, Gia Lai
WhatJobs
Posted 1 day ago
Job Viewed
Job Description
Our client, a growing pharmaceutical company, is looking for a meticulous and detail-oriented Pharmaceutical Quality Control Analyst to join their laboratory team in **Pleiku, Gia Lai, VN**. This is an on-site role critical to ensuring product safety and efficacy.
As a Quality Control Analyst, you will perform a variety of laboratory tests on raw materials, in-process samples, and finished pharmaceutical products to ensure they meet established quality standards and regulatory requirements. Your responsibilities will include operating and maintaining analytical instrumentation such as HPLC, GC, UV-Vis spectrophotometers, and dissolution apparatus; preparing reagents and solutions; accurately documenting all test results according to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP); and investigating out-of-specification (OOS) results and deviations. You will also be involved in method validation activities and contribute to the overall quality assurance of the manufacturing process.
The ideal candidate will have a Bachelor's or Master's degree in Chemistry, Pharmacy, Biology, or a related life science field. Previous experience working in a pharmaceutical quality control laboratory is highly preferred. Strong knowledge of analytical techniques and instrumentation used in the pharmaceutical industry is required. Excellent attention to detail, strong documentation skills, and proficiency with laboratory software are essential. You should have a solid understanding of regulatory guidelines (e.g., FDA, ICH) relevant to pharmaceutical manufacturing. We are seeking a dedicated professional who is committed to upholding the highest standards of quality and safety in pharmaceutical production and possesses excellent teamwork and communication abilities.
As a Quality Control Analyst, you will perform a variety of laboratory tests on raw materials, in-process samples, and finished pharmaceutical products to ensure they meet established quality standards and regulatory requirements. Your responsibilities will include operating and maintaining analytical instrumentation such as HPLC, GC, UV-Vis spectrophotometers, and dissolution apparatus; preparing reagents and solutions; accurately documenting all test results according to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP); and investigating out-of-specification (OOS) results and deviations. You will also be involved in method validation activities and contribute to the overall quality assurance of the manufacturing process.
The ideal candidate will have a Bachelor's or Master's degree in Chemistry, Pharmacy, Biology, or a related life science field. Previous experience working in a pharmaceutical quality control laboratory is highly preferred. Strong knowledge of analytical techniques and instrumentation used in the pharmaceutical industry is required. Excellent attention to detail, strong documentation skills, and proficiency with laboratory software are essential. You should have a solid understanding of regulatory guidelines (e.g., FDA, ICH) relevant to pharmaceutical manufacturing. We are seeking a dedicated professional who is committed to upholding the highest standards of quality and safety in pharmaceutical production and possesses excellent teamwork and communication abilities.
This advertiser has chosen not to accept applicants from your region.
8
Pharmaceutical Quality Control Analyst
60000 Pleiku, Gia Lai
WhatJobs
Posted 1 day ago
Job Viewed
Job Description
Our client is seeking an experienced Pharmaceutical Quality Control Analyst to be based in Pleiku, Gia Lai, VN . This vital role ensures that all manufactured pharmaceutical products meet stringent quality standards and regulatory requirements before they reach the market. The ideal candidate will have a strong background in analytical chemistry and a thorough understanding of Good Manufacturing Practices (GMP).
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Perform a variety of analytical tests on raw materials, in-process samples, and finished products using sophisticated laboratory equipment.
- Ensure all testing is conducted according to approved methods and standard operating procedures (SOPs).
- Accurately document all laboratory results, calculations, and deviations in compliance with GMP guidelines.
- Maintain laboratory equipment, ensuring proper calibration, maintenance, and validation.
- Prepare and standardize reagents and solutions required for testing.
- Participate in method validation and development activities as needed.
- Review and approve batch records and analytical test data.
- Investigate out-of-specification (OOS) results and implement corrective and preventive actions (CAPA).
- Maintain a clean and organized laboratory environment.
- Adhere to all safety protocols and procedures within the laboratory.
Qualifications:
- Bachelor's degree in Chemistry, Pharmacy, Biology, or a related life science field.
- Minimum of 3 years of experience in pharmaceutical quality control or analytical laboratory.
- Proficiency with analytical instrumentation such as HPLC, GC, UV-Vis spectrophotometry, and titration equipment.
- Solid understanding of GMP, GLP, and relevant regulatory guidelines (e.g., FDA, EMA).
- Excellent laboratory techniques and data interpretation skills.
- Strong attention to detail and accuracy in record-keeping.
- Good problem-solving and critical thinking abilities.
- Effective communication and teamwork skills.
- Ability to work independently and manage time efficiently.
- Experience with pharmacopoeial methods (USP, EP, JP) is highly desirable.
This advertiser has chosen not to accept applicants from your region.
9