1 404 Pharmaceutical jobs in Vietnam
Senior Pharmaceutical Quality Assurance Analyst
62001 My Tho, Tien Giang
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Our client is seeking a meticulous and experienced Senior Pharmaceutical Quality Assurance Analyst to join their team in My Tho, Tien Giang, VN . This role is critical for ensuring that all pharmaceutical products meet rigorous quality and regulatory standards throughout the manufacturing process. You will be responsible for developing, implementing, and maintaining quality assurance systems and procedures to guarantee product safety, efficacy, and compliance with Good Manufacturing Practices (GMP) and other relevant regulations. Your analytical skills and attention to detail will be vital in safeguarding the integrity of our client's pharmaceutical offerings.
Key responsibilities include conducting thorough quality audits of manufacturing processes, reviewing batch records, and investigating deviations and out-of-specification results. You will participate in the validation of manufacturing equipment and processes, and ensure that all documentation is accurate, complete, and compliant with regulatory requirements. Developing and implementing corrective and preventive actions (CAPA) to address quality issues will be a core function. You will also be involved in supplier qualification and auditing, and in collaborating with regulatory affairs teams to ensure compliance with national and international pharmaceutical regulations.
The ideal candidate will possess a Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field. A minimum of 6 years of experience in pharmaceutical quality assurance or quality control is required. A strong understanding of GMP, regulatory guidelines (e.g., FDA, ICH), and quality management systems is essential. Excellent analytical, problem-solving, and documentation skills are mandatory. Experience with laboratory testing methods and equipment is beneficial. Strong communication and interpersonal skills are needed to effectively collaborate with various departments and regulatory bodies. This role requires a high level of precision, integrity, and commitment to maintaining the highest quality standards in pharmaceutical manufacturing. If you are a dedicated QA professional looking to make a significant contribution in the pharmaceutical industry, we encourage you to apply.
Key responsibilities include conducting thorough quality audits of manufacturing processes, reviewing batch records, and investigating deviations and out-of-specification results. You will participate in the validation of manufacturing equipment and processes, and ensure that all documentation is accurate, complete, and compliant with regulatory requirements. Developing and implementing corrective and preventive actions (CAPA) to address quality issues will be a core function. You will also be involved in supplier qualification and auditing, and in collaborating with regulatory affairs teams to ensure compliance with national and international pharmaceutical regulations.
The ideal candidate will possess a Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field. A minimum of 6 years of experience in pharmaceutical quality assurance or quality control is required. A strong understanding of GMP, regulatory guidelines (e.g., FDA, ICH), and quality management systems is essential. Excellent analytical, problem-solving, and documentation skills are mandatory. Experience with laboratory testing methods and equipment is beneficial. Strong communication and interpersonal skills are needed to effectively collaborate with various departments and regulatory bodies. This role requires a high level of precision, integrity, and commitment to maintaining the highest quality standards in pharmaceutical manufacturing. If you are a dedicated QA professional looking to make a significant contribution in the pharmaceutical industry, we encourage you to apply.
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Remote Pharmaceutical Research Scientist - Drug Discovery
44000 Hoang Hoa
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Our client is seeking a highly motivated and experienced Remote Pharmaceutical Research Scientist specializing in Drug Discovery. This is a fully remote position that offers the opportunity to contribute to cutting-edge research from your home laboratory or office. You will be instrumental in identifying, validating, and characterizing novel drug targets and therapeutic compounds. Your responsibilities will include designing and executing in vitro and ex vivo experiments, analyzing biological data, and interpreting results to guide the drug development pipeline. This involves leveraging expertise in molecular biology, biochemistry, and pharmacology. You will be expected to conduct thorough literature reviews, develop new experimental protocols, and contribute to the scientific strategy of the research programs. Collaboration is key in this remote role; you will work closely with a multidisciplinary team of scientists, clinicians, and project managers using virtual platforms for communication and data sharing. The ideal candidate will possess strong experimental skills, a deep understanding of disease mechanisms, and a proven track record of success in pharmaceutical research. Proficiency in data analysis software, bioinformatics tools, and scientific writing is essential. We are looking for an innovative thinker with excellent problem-solving abilities, a commitment to scientific rigor, and the capacity to work independently while contributing to a collaborative virtual environment. This role requires a proactive approach to scientific inquiry and a passion for advancing medicine. If you are dedicated to making a significant impact in drug discovery and thrive in a remote research setting, we encourage you to apply.
Responsibilities:
Responsibilities:
- Design and conduct complex biological experiments for drug discovery projects.
- Analyze and interpret large datasets from various experimental platforms.
- Identify and validate novel drug targets and lead compounds.
- Develop and optimize assay methodologies.
- Contribute to the strategic planning and execution of research programs.
- Collaborate effectively with a remote team of scientists and researchers.
- Prepare research reports, presentations, and contribute to publications.
- Stay current with scientific literature and emerging technologies in drug discovery.
- Troubleshoot experimental issues and propose solutions.
- Ph.D. in Pharmacology, Biochemistry, Molecular Biology, or a related life science discipline.
- Minimum of 4 years of post-doctoral or industry experience in pharmaceutical drug discovery.
- Extensive experience with assay development, cell-based assays, and biochemical assays.
- Strong knowledge of medicinal chemistry and pharmacokinetics/pharmacodynamics (PK/PD).
- Proficiency in data analysis software (e.g., GraphPad Prism, R) and bioinformatics tools.
- Excellent scientific writing and presentation skills.
- Demonstrated ability to work independently and collaboratively in a remote setting.
- Strong critical thinking and problem-solving capabilities.
- Experience with relevant therapeutic areas is a plus.
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Pharmaceutical Quality Control Analyst
67000 My Tho, Tien Giang
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Our client is looking for a detail-oriented Pharmaceutical Quality Control Analyst to join their dynamic team in **My Tho, Tien Giang, VN**. This hybrid position requires a blend of laboratory work and analytical reporting, contributing to the rigorous quality assurance of pharmaceutical products. You will be responsible for performing a variety of analytical tests on raw materials, in-process samples, and finished products to ensure they meet strict regulatory and company standards. Your duties will include operating and maintaining sophisticated laboratory equipment, accurately documenting test results, and preparing comprehensive analytical reports. You will also play a role in investigating out-of-specification (OOS) results and participating in method validation studies. The ideal candidate will possess a strong understanding of pharmaceutical quality systems, Good Manufacturing Practices (GMP), and relevant analytical techniques (e.g., HPLC, GC, UV-Vis spectroscopy). Exceptional attention to detail, strong problem-solving skills, and the ability to work collaboratively in a team environment are essential. A bachelor's or master's degree in Pharmacy, Chemistry, Biology, or a related scientific field is required, along with relevant laboratory experience in the pharmaceutical industry. This role offers a significant opportunity to contribute to the development and production of high-quality medicines. We are committed to fostering a productive and innovative work environment in **My Tho, Tien Giang, VN**, offering a competitive salary and opportunities for professional growth.
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Pharmaceutical Research Scientist
52000 Thuy Van
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Our client, a leading pharmaceutical research company, is seeking a dedicated and innovative Pharmaceutical Research Scientist to contribute to groundbreaking drug discovery and development. This is a fully remote position, offering a unique opportunity to work on cutting-edge research from anywhere. You will be responsible for designing and conducting experiments, analyzing data, and contributing to the development of new therapeutic agents. This role requires a strong scientific background, excellent laboratory skills (utilized through remote monitoring and data analysis), and a passion for advancing healthcare.
Key Responsibilities:
Qualifications:
This is a remarkable opportunity for a skilled Pharmaceutical Research Scientist to contribute to significant advancements in medicine from a remote setting. If you are driven by scientific curiosity and possess a strong research background, we encourage you to apply.
Key Responsibilities:
- Design, execute, and optimize in vitro and in vivo experimental protocols for drug discovery and development.
- Analyze and interpret complex biological and chemical data, drawing accurate conclusions.
- Utilize advanced computational tools and databases for data analysis and hypothesis generation.
- Prepare detailed research reports, scientific presentations, and manuscripts for publication.
- Collaborate closely with cross-functional teams, including chemists, biologists, and pharmacologists.
- Maintain accurate and up-to-date laboratory notebooks and research records.
- Stay abreast of the latest scientific literature and technological advancements in the pharmaceutical industry.
- Contribute to the development of new research methodologies and experimental designs.
- Participate in scientific discussions and provide critical feedback on research projects.
- Ensure compliance with all safety regulations and ethical guidelines in research.
- Assist in the preparation of grant proposals and regulatory submissions.
- Manage research projects, ensuring timely completion of milestones.
Qualifications:
- Ph.D. or Master's degree in Pharmacology, Molecular Biology, Biochemistry, or a related life science discipline.
- Minimum of 3-5 years of post-doctoral or relevant industry research experience.
- Proven expertise in (Specify Area, e.g., drug metabolism, cellular signaling, medicinal chemistry).
- Strong understanding of drug discovery and development processes.
- Proficiency in data analysis software (e.g., GraphPad Prism, R, Python) and bioinformatics tools.
- Excellent analytical, problem-solving, and critical thinking skills.
- Exceptional written and verbal communication skills.
- Ability to work independently and effectively within a remote research team.
- Experience with laboratory automation and high-throughput screening is an advantage.
- A passion for scientific inquiry and a commitment to innovation.
This is a remarkable opportunity for a skilled Pharmaceutical Research Scientist to contribute to significant advancements in medicine from a remote setting. If you are driven by scientific curiosity and possess a strong research background, we encourage you to apply.
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Senior Pharmaceutical Quality Assurance Specialist
400000 Nam Dinh , Nam Dinh
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Our client is looking for a meticulous and experienced Senior Pharmaceutical Quality Assurance Specialist to join their esteemed team in **Nam Dinh, Nam Dinh, VN**. This critical role involves ensuring that all pharmaceutical products manufactured by our client meet the highest standards of quality, safety, and efficacy, adhering strictly to national and international regulatory guidelines. You will be responsible for developing, implementing, and maintaining robust quality management systems (QMS), including SOPs, batch record reviews, and deviation investigations. The ideal candidate will possess a thorough understanding of Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant pharmaceutical quality standards. Your responsibilities will include conducting internal audits, performing risk assessments, and validating manufacturing processes and equipment to ensure compliance. You will also play a key role in regulatory inspections, preparing necessary documentation, and acting as a point of contact for health authorities. Excellent analytical and problem-solving skills are essential for identifying root causes of quality issues and implementing effective corrective and preventive actions (CAPA). This position requires strong attention to detail, the ability to work independently as well as collaboratively with cross-functional teams (e.g., production, R&D, regulatory affairs), and outstanding written and verbal communication skills. A Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific field is required, along with significant experience (typically 5+ years) in pharmaceutical quality assurance or quality control. Familiarity with pharmaceutical documentation, validation principles, and quality risk management is crucial. This is an opportunity to contribute to the production of life-saving medications and ensure patient safety. The successful candidate will be proactive, results-oriented, and committed to upholding the highest standards of pharmaceutical quality.
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Remote Senior Pharmaceutical Researcher
70000 An Thanh
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This is a fully remote position. Our client, a renowned pharmaceutical company, is seeking a highly qualified Remote Senior Pharmaceutical Researcher to contribute to cutting-edge drug discovery and development. In this vital role, you will conduct advanced research, design and execute experiments, analyze complex data sets, and contribute to the scientific literature. Your expertise will be crucial in identifying and validating novel therapeutic targets, developing innovative drug candidates, and ensuring the efficacy and safety of pharmaceutical products. You will collaborate with a multidisciplinary team of scientists and researchers, both domestically and internationally, all working remotely. The ideal candidate possesses a strong background in pharmacology, medicinal chemistry, or a related life science discipline, with a proven track record of successful research projects and publications. You should be proficient in advanced research methodologies, laboratory techniques, and scientific data analysis tools. A PhD or equivalent advanced degree is required. This is an exceptional opportunity to advance pharmaceutical science from the comfort of your home office. Responsibilities include:
- Conducting original research in pharmaceutical sciences.
- Designing and performing complex experiments and analytical studies.
- Analyzing and interpreting scientific data, drawing robust conclusions.
- Developing and optimizing experimental protocols and methodologies.
- Contributing to the discovery and development of new therapeutic agents.
- Preparing scientific reports, publications, and presentations.
- Collaborating with internal and external research partners.
- Mentoring junior researchers and scientific staff.
- Staying updated with the latest advancements in pharmaceutical research.
- Ensuring compliance with research ethics and regulatory guidelines.
- PhD in Pharmacology, Medicinal Chemistry, Biochemistry, or a related field.
- Demonstrated experience in pharmaceutical research and drug development.
- Expertise in relevant scientific techniques and methodologies.
- Strong publication record in peer-reviewed journals.
- Excellent analytical, problem-solving, and critical thinking skills.
- Proficiency in scientific data analysis software.
- Strong written and verbal communication skills for scientific reporting.
- Ability to work independently and effectively in a remote research setting.
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5
Clinical Research Associate
94000 Can Tho , Can Tho
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We are seeking a dedicated and detail-oriented Clinical Research Associate (CRA) to support our ongoing pharmaceutical research projects in Can Tho, Can Tho, VN . The CRA will be instrumental in ensuring the quality and integrity of clinical trials by monitoring study sites, verifying data accuracy, and ensuring adherence to protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements. Your responsibilities will include site selection and initiation visits, conducting routine monitoring visits (on-site and remote), and performing close-out visits. You will be responsible for reviewing case report forms (CRFs), source documents, and study records to ensure data accuracy and completeness. The role involves proactive identification and resolution of site issues, including protocol deviations and data discrepancies. You will also play a key part in training site staff on study procedures and regulatory requirements. Building and maintaining strong working relationships with investigators, site staff, and internal study teams is crucial. You will prepare accurate and timely monitoring visit reports and ensure essential documents are complete and up-to-date. This position requires a thorough understanding of the drug development process and clinical trial management. Exceptional organizational skills and the ability to manage multiple tasks and priorities effectively are essential. A commitment to patient safety and data integrity is paramount. Experience in therapeutic areas such as oncology, cardiology, or neurology is a significant plus. The ideal candidate will possess excellent communication skills, both written and verbal, and the ability to work independently and as part of a team. Frequent travel to study sites within the region may be required.
Responsibilities:
Responsibilities:
- Conduct site monitoring visits to ensure protocol compliance.
- Verify the accuracy and completeness of clinical trial data.
- Ensure adherence to GCP, SOPs, and regulatory guidelines.
- Train site staff on study-specific procedures.
- Manage site communication and problem resolution.
- Review source documents and case report forms.
- Prepare comprehensive monitoring visit reports.
- Maintain essential study documents and regulatory files.
- Contribute to site selection and initiation processes.
- Bachelor's degree in a life science, nursing, or related field.
- Minimum of 3 years of experience as a Clinical Research Associate.
- In-depth knowledge of GCP and regulatory requirements.
- Experience with electronic data capture (EDC) systems.
- Strong understanding of clinical trial processes.
- Excellent analytical and problem-solving skills.
- Effective communication and interpersonal abilities.
- Willingness to travel to study sites as needed.
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6
Pharmaceutical Quality Assurance Specialist
25000 Phuong Son
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WhatJobs is recruiting a meticulous and experienced Pharmaceutical Quality Assurance Specialist to join our team in Thai Nguyen, Thai Nguyen, VN . This role is critical in ensuring that our pharmaceutical products meet the highest standards of quality, safety, and efficacy. You will be responsible for developing, implementing, and maintaining quality management systems and ensuring compliance with regulatory standards such as cGMP (current Good Manufacturing Practices). Your duties will include conducting internal audits, reviewing batch records, investigating deviations and out-of-specification (OOS) results, and participating in CAPA (Corrective and Preventive Actions) implementation. You will also be involved in process validation, equipment qualification, and change control management. Collaborating with various departments, including manufacturing, quality control, and regulatory affairs, is essential to ensure a cohesive approach to quality. The ideal candidate will have a strong understanding of pharmaceutical manufacturing processes, quality control procedures, and relevant regulatory guidelines. Excellent analytical skills, attention to detail, and the ability to interpret complex data are crucial. You should be proficient in risk assessment and mitigation strategies. This position offers the opportunity to contribute significantly to the success of our pharmaceutical development and manufacturing operations. Your ability to work effectively in a team environment, as well as independently, will be highly valued. Strong documentation and report-writing skills are a must. Experience with validation protocols and reports is a significant advantage. If you are passionate about ensuring product quality and have a keen eye for detail in a regulated industry, we encourage you to apply.
Responsibilities:
Responsibilities:
- Implement and maintain Quality Management Systems (QMS).
- Conduct internal audits and ensure compliance with cGMP.
- Review and approve batch manufacturing records.
- Investigate deviations, OOS results, and customer complaints.
- Develop and implement CAPAs.
- Participate in validation activities (process, equipment, cleaning).
- Manage change control processes.
- Collaborate with cross-functional teams on quality-related issues.
- Ensure all quality documentation is accurate and maintained.
- Stay updated on regulatory requirements and industry best practices.
- Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
- Minimum of 4 years of experience in pharmaceutical Quality Assurance or Quality Control.
- In-depth knowledge of cGMP and other relevant regulatory guidelines (FDA, EMA).
- Experience with pharmaceutical manufacturing processes.
- Proficiency in quality risk management and deviation investigations.
- Strong analytical and problem-solving skills.
- Excellent documentation and report-writing abilities.
- Ability to work effectively both independently and as part of a team.
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7
Remote Pharmaceutical Quality Assurance Specialist
60000 Hoi An
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Our client, a leading pharmaceutical entity, is searching for a meticulous and experienced Remote Pharmaceutical Quality Assurance Specialist. This position is entirely remote, providing flexibility for talented individuals nationwide.
Responsibilities:
Location: Buon Ma Thuot, Dak Lak, VN (Remote)
Responsibilities:
- Develop, implement, and maintain the company's quality management system (QMS) in compliance with pharmaceutical regulations (e.g., GMP, GDP).
- Conduct internal audits and inspections of manufacturing processes, documentation, and facilities to ensure adherence to quality standards.
- Review and approve batch records, validation protocols, and other critical quality documents.
- Investigate deviations, out-of-specification (OOS) results, and customer complaints, implementing corrective and preventive actions (CAPAs).
- Manage change control processes and assess the impact of proposed changes on product quality.
- Prepare for and participate in regulatory inspections and audits by health authorities.
- Develop and deliver quality training programs to relevant personnel.
- Monitor key quality indicators (KQIs) and prepare quality metrics reports.
- Stay current with evolving regulatory requirements and industry best practices in pharmaceutical quality assurance.
- Collaborate with cross-functional teams to ensure product quality and regulatory compliance throughout the product lifecycle.
- Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science field.
- Minimum of 4 years of experience in pharmaceutical quality assurance or quality control.
- In-depth knowledge of Good Manufacturing Practices (GMP), Good Distribution Practices (GDP), and other relevant regulatory guidelines.
- Experience with quality management systems, audits, CAPA, and change control.
- Strong analytical skills and attention to detail.
- Excellent written and verbal communication skills, with the ability to document findings clearly and concisely.
- Ability to work independently and manage workload effectively in a remote setting.
- Proficiency in using QMS software and Microsoft Office Suite.
- Problem-solving aptitude and a proactive approach to quality issues.
- Understanding of pharmaceutical manufacturing processes is essential.
Location: Buon Ma Thuot, Dak Lak, VN (Remote)
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8
Senior Pharmaceutical Regulatory Affairs Associate
60000 Pleiku, Gia Lai
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Join a leading pharmaceutical company as a Senior Pharmaceutical Regulatory Affairs Associate, where you will play a critical role in ensuring compliance with global regulatory standards. This hybrid position allows for a blend of focused in-office collaboration and flexible remote work. You will be responsible for preparing, reviewing, and submitting regulatory documentation for new drug applications, variations, and renewals across various markets. Your expertise will be vital in interpreting and applying complex regulatory guidelines, ensuring that our products meet all necessary legal and scientific requirements. This involves close collaboration with R&D, clinical affairs, quality assurance, and marketing departments to gather data and ensure the accuracy and completeness of submissions. You will manage regulatory timelines, track submission status, and proactively address any regulatory challenges that may arise. A significant part of your role will involve staying abreast of evolving regulatory landscapes, new legislation, and industry best practices, translating this knowledge into actionable strategies for the company. You will also be involved in preparing responses to regulatory agency queries and managing post-approval commitments. The ideal candidate will possess a strong scientific background, a comprehensive understanding of pharmaceutical development processes, and a proven track record in regulatory affairs. Excellent analytical, written, and verbal communication skills are essential, as is the ability to manage multiple projects simultaneously. This role requires a detail-oriented individual with a high level of integrity and a commitment to patient safety. You will contribute to bringing innovative medicines to patients by navigating the complex regulatory pathways with expertise and precision. If you are driven by scientific rigor and possess a strategic approach to regulatory compliance, we encourage you to apply and make a significant impact on our mission.
Key Responsibilities:
Key Responsibilities:
- Prepare and submit regulatory dossiers (e.g., NDAs, MAAs, variations).
- Review and approve labeling, promotional materials, and other regulated documents.
- Interpret and apply global regulatory guidelines and regulations.
- Liaise with health authorities and regulatory agencies.
- Manage post-approval regulatory activities and lifecycle management.
- Provide regulatory input and strategy for product development projects.
- Collaborate with cross-functional teams (R&D, Clinical, Quality, Marketing).
- Conduct regulatory intelligence gathering and analysis.
- Prepare responses to regulatory agency questions and deficiency letters.
- Ensure compliance with GxP and other relevant quality systems.
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
- Minimum of 5 years of experience in pharmaceutical regulatory affairs.
- In-depth knowledge of regulatory submission processes and guidelines (e.g., ICH, FDA, EMA).
- Proven experience in preparing and submitting regulatory dossiers.
- Strong analytical and problem-solving skills.
- Excellent written and verbal communication abilities.
- Ability to manage multiple projects and meet tight deadlines.
- Proficiency in regulatory information management systems.
- Attention to detail and commitment to accuracy.
- Experience with hybrid work models and cross-functional team collaboration.
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