1 674 Industrial Engineering 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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Senior Industrial Process Engineer
30000 An Thanh
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Our client is seeking a highly skilled Senior Industrial Process Engineer to optimize manufacturing and operational processes. This hybrid role, based in **Vung Tau, Ba Ria–Vung Tau, VN**, will involve analyzing existing production systems, identifying areas for improvement, and implementing solutions to enhance efficiency, reduce waste, and improve product quality. You will be responsible for designing, developing, and implementing new manufacturing processes, ensuring they are safe, cost-effective, and meet all regulatory requirements. A key focus will be on applying Lean Manufacturing principles and Six Sigma methodologies to drive continuous improvement initiatives. The ideal candidate will have a strong background in industrial engineering, process optimization, and statistical analysis. Proficiency in process simulation software and CAD tools is highly desirable. You will work closely with production teams, quality assurance, and engineering departments to troubleshoot issues and implement best practices. Excellent problem-solving skills, data analysis capabilities, and strong project management experience are essential. The ability to lead cross-functional teams and effectively communicate technical information to both technical and non-technical audiences is crucial. This position requires a blend of on-site presence for hands-on analysis and team collaboration, alongside remote work capabilities for data analysis and reporting. We are looking for a motivated engineer passionate about improving operational performance and driving innovation in manufacturing processes.
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Industrial Automation Engineer
95000 Long Xuyen, An Giang
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Our client is seeking a highly skilled Industrial Automation Engineer for their facility in Long Xuyen, An Giang, VN . This role requires hands-on expertise in designing, implementing, and maintaining automated systems for manufacturing processes. You will be responsible for improving efficiency, quality, and safety through the application of automation technologies, including PLC programming, HMI development, robotics, and SCADA systems. The ideal candidate will have a strong background in industrial control systems, a solid understanding of electrical and mechanical principles, and experience with various automation hardware and software platforms.
Key Responsibilities:
Key Responsibilities:
- Design, program, and commission automated control systems using PLCs, HMIs, and SCADA.
- Develop and implement robotic solutions for manufacturing processes.
- Troubleshoot and maintain existing automation equipment and systems.
- Optimize manufacturing processes through the application of automation technologies.
- Collaborate with cross-functional teams on new equipment installations and upgrades.
- Ensure compliance with safety standards and regulations.
- Develop technical documentation, including schematics, manuals, and programming logic.
- Identify opportunities for automation improvements and cost savings.
- Provide technical support and training to operations staff.
- Participate in project planning and execution for new automation initiatives.
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2
Industrial Process Engineer
60000 Hoi An
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Our client is seeking an experienced Industrial Process Engineer to contribute to their manufacturing operations located in **Buon Ma Thuot, Dak Lak, VN**. This role is essential for optimizing production processes, improving efficiency, and ensuring the highest standards of quality and safety. You will be responsible for analyzing existing manufacturing workflows, identifying areas for improvement, and implementing innovative solutions to enhance productivity and reduce waste. This will involve working closely with production teams, quality control personnel, and management to develop and execute process improvements. Key duties include designing and testing new process layouts, developing standard operating procedures (SOPs), and conducting performance monitoring to ensure adherence to specifications. You will also be involved in troubleshooting production issues, implementing corrective actions, and driving continuous improvement initiatives. The ideal candidate will have a strong foundation in industrial engineering principles, with a proven ability to apply quantitative methods to process analysis and optimization. Excellent analytical, problem-solving, and project management skills are required. You should be proficient in process simulation software and have a solid understanding of lean manufacturing and Six Sigma methodologies. A bachelor's degree in Industrial Engineering or a related field is mandatory, along with several years of relevant experience in a manufacturing or industrial setting. This is a critical role that offers the chance to make a significant impact on our client's operational success. Join our dedicated team in **Buon Ma Thuot, Dak Lak, VN** and help shape the future of our production.
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Industrial Process Engineer
67000 My Tho, Tien Giang
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Are you an innovative Industrial Process Engineer passionate about optimizing manufacturing operations? Our client is seeking a skilled professional to join their globally distributed team. This is a fully remote role, allowing you to leverage your expertise to improve efficiency, quality, and cost-effectiveness in industrial processes. You will be responsible for analyzing existing production systems, identifying bottlenecks, and implementing process improvements. This involves utilizing advanced engineering principles, data analysis, and collaborative problem-solving with cross-functional teams.
Key Responsibilities:
Qualifications:
This is an excellent opportunity for an experienced Industrial Process Engineer to contribute significantly to our client's success while enjoying the flexibility of a remote career. If you are driven by innovation and efficiency, we encourage you to apply.
Key Responsibilities:
- Analyze and design industrial processes to maximize efficiency, productivity, and safety.
- Develop and implement process improvements and optimization strategies using lean manufacturing and Six Sigma principles.
- Conduct feasibility studies and pilot tests for new processes and technologies.
- Create and maintain process flow diagrams, standard operating procedures (SOPs), and technical documentation.
- Troubleshoot production issues and implement root cause analysis to prevent recurrence.
- Collaborate with R&D, production, and quality control teams to integrate new products and processes.
- Design and implement systems for process monitoring and control.
- Evaluate and recommend new equipment and technologies to enhance production capabilities.
- Train production staff on new processes and best practices.
- Manage process engineering projects from concept to implementation, ensuring successful outcomes.
- Monitor key performance indicators (KPIs) for process efficiency and product quality.
- Ensure compliance with environmental, health, and safety regulations.
Qualifications:
- Bachelor's degree in Industrial Engineering, Mechanical Engineering, Chemical Engineering, or a related field.
- Minimum of 5 years of experience in process engineering within a manufacturing or industrial environment.
- Proven experience in process optimization, lean manufacturing, and Six Sigma methodologies.
- Strong analytical and problem-solving skills with a data-driven approach.
- Proficiency in process simulation software and CAD tools.
- Excellent understanding of manufacturing principles and production systems.
- Strong communication and interpersonal skills, with the ability to collaborate effectively in a remote team.
- Experience with project management and leading improvement initiatives.
- Familiarity with quality management systems (e.g., ISO 9001).
- Ability to interpret technical drawings and specifications.
- A proactive and continuous improvement mindset.
This is an excellent opportunity for an experienced Industrial Process Engineer to contribute significantly to our client's success while enjoying the flexibility of a remote career. If you are driven by innovation and efficiency, we encourage you to apply.
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Senior Industrial Engineer
800000 My Tho, Tien Giang
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Our client is seeking a highly analytical and process-oriented Senior Industrial Engineer for a fully remote position. You will play a pivotal role in optimizing complex systems of people, materials, information, equipment, and energy. Your expertise will be directed towards improving efficiency, productivity, quality, and safety across various operational domains. Key responsibilities include analyzing operational workflows, identifying bottlenecks and areas for improvement, developing and implementing process enhancements, conducting time and motion studies, and utilizing statistical methods and simulation tools to model and analyze system performance. You will also be involved in designing manufacturing processes, recommending equipment upgrades, and developing quality control systems. The ideal candidate holds a Bachelor's or Master's degree in Industrial Engineering or a related field, with substantial professional experience in process improvement and system optimization. Strong proficiency in simulation software (e.g., Arena, AnyLogic), statistical analysis tools (e.g., Minitab), and CAD software is highly desirable. Excellent analytical, problem-solving, and project management skills are essential. The ability to communicate technical information clearly and effectively to diverse stakeholders, both written and verbal, is crucial. This remote role requires a proactive individual with a keen understanding of lean manufacturing principles, Six Sigma methodologies, and a commitment to driving operational excellence from a remote work environment.
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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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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
Remote Industrial Automation Engineer
46000 Hoang Hoa
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Our client is seeking a skilled and innovative Remote Industrial Automation Engineer to design, implement, and optimize automated systems for manufacturing processes. This is a fully remote opportunity.
Responsibilities:
Location: Thanh Hoa, Thanh Hoa, VN (Remote)
Responsibilities:
- Design and develop automation solutions for industrial processes, including PLC programming, HMI development, and SCADA system integration.
- Select and specify appropriate hardware components such as sensors, actuators, motors, and control systems.
- Program and configure Programmable Logic Controllers (PLCs) using various software platforms (e.g., Rockwell Studio 5000, Siemens TIA Portal).
- Develop user-friendly Human-Machine Interfaces (HMIs) for process control and monitoring.
- Integrate automation systems with enterprise resource planning (ERP) and manufacturing execution systems (MES).
- Troubleshoot and debug automation systems, identifying and resolving technical issues remotely.
- Conduct system testing and commissioning, ensuring functionality and performance meet design specifications.
- Create and maintain technical documentation, including control narratives, P&IDs, and user manuals.
- Collaborate with clients and internal teams to define project requirements and ensure successful implementation.
- Stay current with advancements in industrial automation technologies, including robotics, IoT, and artificial intelligence.
- Bachelor's degree in Electrical Engineering, Mechanical Engineering, Computer Engineering, or a related field.
- Minimum of 4 years of experience in industrial automation and control systems engineering.
- Proficiency in PLC programming (Allen-Bradley, Siemens, Omron, etc.) and HMI/SCADA software development.
- Experience with industrial networking protocols (e.g., Ethernet/IP, Profibus, Modbus).
- Strong understanding of automation principles, control theory, and system integration.
- Ability to read and interpret electrical schematics and P&IDs.
- Excellent problem-solving and analytical skills for remote troubleshooting.
- Strong communication and collaboration skills to work effectively with distributed teams.
- Self-motivated and capable of managing projects independently in a remote work environment.
- Familiarity with robotic systems and motion control is a plus.
Location: Thanh Hoa, Thanh Hoa, VN (Remote)
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