431 Quality Specialist jobs in Vietnam
Pharmaceutical Quality Assurance Specialist
53000 Thuy Van
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Job Description
We are seeking a highly meticulous and experienced Pharmaceutical Quality Assurance Specialist for a fully remote position. This role is vital in ensuring our pharmaceutical products meet the highest standards of quality, safety, and efficacy. You will be responsible for developing, implementing, and maintaining robust quality assurance systems and procedures. Your expertise will be critical in ensuring compliance with regulatory requirements and driving continuous improvement in our pharmaceutical operations. This is a fully remote role.
Key Responsibilities:
Qualifications:
This is an exceptional opportunity for a dedicated QA professional to contribute significantly to the pharmaceutical sector from a remote setting.
Key Responsibilities:
- Develop, implement, and maintain the company's Quality Management System (QMS) in accordance with international standards (e.g., GMP, ISO).
- Conduct internal audits and quality assessments of pharmaceutical processes and documentation.
- Review and approve batch records, specifications, validation protocols, and reports.
- Monitor and analyze quality control data to identify trends and potential areas for improvement.
- Investigate deviations, out-of-specification results, and customer complaints, implementing corrective and preventive actions (CAPA).
- Ensure compliance with relevant regulatory requirements from health authorities.
- Prepare for and participate in external audits and regulatory inspections.
- Collaborate with cross-functional teams, including R&D, manufacturing, and regulatory affairs, to ensure quality throughout the product lifecycle.
- Contribute to the training of personnel on quality assurance principles and practices.
- Stay abreast of evolving pharmaceutical regulations and quality standards.
Qualifications:
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field.
- Minimum of 5 years of experience in Quality Assurance or Quality Control within the pharmaceutical industry.
- In-depth knowledge of Good Manufacturing Practices (GMP) and other relevant pharmaceutical quality standards.
- Proven experience in developing and implementing QMS, conducting audits, and managing CAPA.
- Strong analytical, problem-solving, and critical thinking skills.
- Excellent written and verbal communication skills, with the ability to clearly document findings and recommendations.
- Proficiency in using quality management software and data analysis tools.
- Ability to work independently, manage multiple projects, and meet deadlines in a remote environment.
- Detail-oriented with a strong commitment to quality and compliance.
- Experience with regulatory submissions is a plus.
This is an exceptional opportunity for a dedicated QA professional to contribute significantly to the pharmaceutical sector from a remote setting.
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Pharmaceutical Quality Assurance Specialist
55000 Hoa Sơn
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Our client, a growing pharmaceutical company, is seeking a detail-oriented and experienced Pharmaceutical Quality Assurance Specialist for their facility in Quy Nhon, Binh Dinh, VN . This is a critical on-site role responsible for ensuring that all pharmaceutical products meet stringent quality standards and regulatory requirements throughout the manufacturing process. Your expertise will be vital in maintaining product integrity and compliance.
Responsibilities:
Responsibilities:
- Develop, implement, and maintain Quality Management Systems (QMS) for pharmaceutical manufacturing.
- Ensure compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant regulatory guidelines.
- Review and approve batch records, analytical data, and other quality-related documentation.
- Conduct internal audits and inspections to assess compliance with quality standards.
- Investigate deviations, out-of-specification (OOS) results, and customer complaints, implementing corrective and preventive actions (CAPAs).
- Participate in external audits from regulatory agencies and customers.
- Monitor and analyze quality control data to identify trends and areas for improvement.
- Collaborate with manufacturing, R&D, and other departments to ensure quality is integrated into all stages of product lifecycle.
- Develop and deliver training programs on quality assurance principles and practices for staff.
- Manage and maintain quality control equipment calibration and validation schedules.
- Write and revise Standard Operating Procedures (SOPs) and quality policies.
- Perform risk assessments and implement mitigation strategies.
- Release finished products after reviewing all necessary quality documentation.
- Stay updated on current regulatory requirements and industry best practices.
- Contribute to the continuous improvement of quality processes.
- Bachelor's degree in Pharmacy, Chemistry, Biology, or a related science field. Advanced degree is a plus.
- Minimum of 3-5 years of experience in Quality Assurance or Quality Control within the pharmaceutical industry.
- In-depth knowledge of GMP, FDA, and other relevant pharmaceutical regulations.
- Experience with QMS, CAPA systems, and deviation management.
- Strong analytical, problem-solving, and documentation skills.
- Excellent attention to detail and accuracy.
- Proficiency in Microsoft Office Suite.
- Good communication and interpersonal skills.
- Ability to work effectively both independently and as part of a team.
- Experience with validation processes (process, equipment, cleaning) is desirable.
This advertiser has chosen not to accept applicants from your region.
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Pharmaceutical Quality Assurance Specialist
320000 An Thanh
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Our client, a dynamic pharmaceutical company, is seeking a dedicated Pharmaceutical Quality Assurance Specialist. This role offers a fully remote work opportunity, allowing you to contribute to ensuring the highest standards of quality and compliance within the pharmaceutical manufacturing process from anywhere. You will be instrumental in upholding our client's commitment to safety and efficacy.
Responsibilities:
Responsibilities:
- Develop, implement, and maintain the Quality Management System (QMS) in compliance with GMP, ICH, and other relevant regulatory guidelines.
- Conduct internal audits and inspections to ensure adherence to quality standards.
- Review and approve batch records, validation protocols, and manufacturing documentation.
- Investigate deviations, out-of-specification (OOS) results, and customer complaints, implementing corrective and preventive actions (CAPAs).
- Participate in external audits and inspections by regulatory authorities and clients.
- Collaborate with manufacturing, R&D, and regulatory affairs departments to resolve quality issues.
- Develop and deliver quality training programs to personnel.
- Monitor and analyze quality control data to identify trends and areas for improvement.
- Contribute to the qualification and validation of equipment and processes.
- Stay current with evolving regulatory requirements and industry best practices in the pharmaceutical sector.
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
- Minimum of 4 years of experience in Quality Assurance within the pharmaceutical industry.
- In-depth knowledge of Good Manufacturing Practices (GMP) and other relevant pharmaceutical regulations.
- Experience with QMS, CAPA systems, and deviation management.
- Proficiency in reviewing technical documents and performing quality audits.
- Strong analytical and problem-solving skills.
- Excellent written and verbal communication abilities.
- Ability to work independently and collaboratively in a remote team environment.
- Meticulous attention to detail and commitment to quality.
- Experience with sterile manufacturing or specific drug product categories is an advantage.
This advertiser has chosen not to accept applicants from your region.
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Pharmaceutical Quality Assurance Specialist
90000 Rach Gia, Kien Giang
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Job Description
Our client is seeking a meticulous and experienced Pharmaceutical Quality Assurance Specialist to join their regulatory compliance team. This is a fully remote role, vital for ensuring that all pharmaceutical products meet stringent quality standards and regulatory requirements. You will be responsible for reviewing and approving batch records, investigating deviations and out-of-specification results, and implementing corrective and preventive actions (CAPA). The ideal candidate possesses a strong understanding of Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and relevant pharmaceutical regulations. Your role will involve developing and maintaining quality systems, conducting internal audits, and participating in external audits. You will work closely with R&D, manufacturing, and regulatory affairs departments to ensure product quality throughout the entire lifecycle. This role requires exceptional attention to detail, strong analytical skills, and the ability to interpret and apply complex quality standards. Excellent written and verbal communication skills are essential for documenting findings, communicating with cross-functional teams, and preparing regulatory submissions. We are looking for individuals who are proactive in identifying and resolving quality issues and are committed to maintaining the highest standards of pharmaceutical quality and patient safety. Your contribution will be crucial in ensuring the integrity and compliance of our client's pharmaceutical products. This is an excellent opportunity for a quality professional to contribute to a leading pharmaceutical company from a remote setting. Join us in upholding the highest standards of pharmaceutical excellence.
Key Responsibilities:
Key Responsibilities:
- Review and approve batch production and control records.
- Investigate deviations, CAPAs, and out-of-specification results.
- Ensure compliance with GMP, GLP, and other regulatory guidelines.
- Develop, implement, and maintain quality management systems.
- Conduct internal audits and support external audits.
- Collaborate with manufacturing and R&D on quality-related issues.
- Analyze quality data and identify trends.
- Prepare quality documentation and reports.
- Participate in validation activities.
- Stay current with pharmaceutical regulations and quality standards.
- Proven experience as a Quality Assurance Specialist in the pharmaceutical industry.
- In-depth knowledge of GMP, GLP, and regulatory requirements (e.g., FDA, EMA).
- Experience with quality management systems and audit processes.
- Strong analytical and problem-solving skills.
- Excellent documentation and communication abilities.
- Ability to work independently and manage responsibilities in a remote environment.
- Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
This advertiser has chosen not to accept applicants from your region.
3
Pharmaceutical Quality Assurance Specialist
30000 Thai Binh , Thai Binh
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Job Description
Our client is seeking a meticulous and experienced Pharmaceutical Quality Assurance Specialist for their operations in Thai Binh, Thai Binh, VN . This role is critical in ensuring that all pharmaceutical products meet stringent quality standards and comply with regulatory requirements. You will be responsible for developing, implementing, and maintaining quality assurance systems and procedures throughout the product lifecycle, from raw material sourcing to finished product release. The ideal candidate will possess a comprehensive understanding of Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant pharmaceutical quality standards.
Key responsibilities include conducting regular audits of manufacturing processes, reviewing batch records, and investigating deviations and non-conformances. You will be involved in validating manufacturing equipment and processes, as well as developing and executing quality control tests. The ability to analyze data, identify root causes of quality issues, and implement corrective and preventive actions (CAPAs) is essential. We are looking for a detail-oriented individual with strong analytical and problem-solving skills, coupled with excellent written and verbal communication abilities. Proficiency in documentation management and a thorough understanding of regulatory submissions and compliance are highly valued. Experience in the pharmaceutical or biotechnology industry is a prerequisite. You will play a key role in ensuring the safety and efficacy of pharmaceutical products and maintaining the company's commitment to quality excellence. Collaboration with R&D, production, and regulatory affairs teams will be integral to success in this role. Your expertise will contribute directly to patient safety and product integrity.
Key responsibilities include conducting regular audits of manufacturing processes, reviewing batch records, and investigating deviations and non-conformances. You will be involved in validating manufacturing equipment and processes, as well as developing and executing quality control tests. The ability to analyze data, identify root causes of quality issues, and implement corrective and preventive actions (CAPAs) is essential. We are looking for a detail-oriented individual with strong analytical and problem-solving skills, coupled with excellent written and verbal communication abilities. Proficiency in documentation management and a thorough understanding of regulatory submissions and compliance are highly valued. Experience in the pharmaceutical or biotechnology industry is a prerequisite. You will play a key role in ensuring the safety and efficacy of pharmaceutical products and maintaining the company's commitment to quality excellence. Collaboration with R&D, production, and regulatory affairs teams will be integral to success in this role. Your expertise will contribute directly to patient safety and product integrity.
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Pharmaceutical Quality Assurance Specialist
20000 Phuong Son
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Job Description
Our client, a leading pharmaceutical company, is seeking a meticulous and dedicated Pharmaceutical Quality Assurance Specialist to join their team in Thai Nguyen, Thai Nguyen, VN . This critical role ensures that all pharmaceutical products meet the highest standards of quality and safety throughout the manufacturing process. You will be responsible for developing, implementing, and maintaining robust quality assurance systems and procedures in compliance with regulatory requirements such as GMP (Good Manufacturing Practices). Your duties will include conducting regular inspections of production facilities, reviewing batch records, analyzing product samples, and investigating any deviations or non-conformities. You will also play a key role in validating manufacturing processes and equipment, and in training staff on quality control procedures. The ideal candidate will possess a strong scientific background, meticulous attention to detail, and a thorough understanding of pharmaceutical regulations and quality management principles. Excellent analytical skills and the ability to work effectively within a team are crucial. This is an excellent opportunity to contribute to the development and production of life-saving medicines.
Key Responsibilities:
Key Responsibilities:
- Develop, implement, and maintain quality assurance programs and SOPs.
- Conduct internal audits and inspections of manufacturing processes and facilities.
- Review and approve batch records, validation protocols, and quality-related documents.
- Investigate deviations, CAPAs (Corrective and Preventive Actions), and customer complaints.
- Perform product release testing and ensure compliance with specifications.
- Collaborate with R&D, production, and regulatory affairs teams to ensure product quality.
- Train personnel on quality control procedures and GMP requirements.
- Stay updated on relevant industry regulations and quality standards.
- Participate in external audits by regulatory agencies.
- Contribute to continuous improvement initiatives for quality systems.
- Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
- Minimum of 3 years of experience in pharmaceutical quality assurance or quality control.
- In-depth knowledge of GMP, ICH guidelines, and other relevant pharmaceutical regulations.
- Experience with quality management systems (QMS) and audit procedures.
- Strong analytical and problem-solving skills.
- Excellent documentation and technical writing skills.
- Proficiency in MS Office and quality management software.
- Ability to work effectively in a team-oriented environment.
This advertiser has chosen not to accept applicants from your region.
5
Pharmaceutical Quality Assurance Specialist
55000 Hoa Sơn
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Our client, a prominent pharmaceutical company, is looking for a meticulous and experienced Pharmaceutical Quality Assurance Specialist to join their team in **Da Nang, Da Nang, VN**. This on-site role is crucial for ensuring the highest standards of quality and compliance throughout the pharmaceutical manufacturing process. You will be responsible for developing, implementing, and maintaining quality systems and procedures in accordance with regulatory requirements (e.g., GMP, GDP). Key duties include reviewing and approving batch records, performing internal audits, and managing deviations and change controls. You will also participate in external audits and inspections and contribute to the continuous improvement of quality processes. The ideal candidate will have a strong understanding of pharmaceutical manufacturing, quality control principles, and regulatory affairs. Excellent analytical skills, attention to detail, and strong documentation abilities are essential. You will work closely with manufacturing, R&D, and regulatory departments to ensure product quality and patient safety. Responsibilities also include training personnel on quality-related matters and investigating quality issues to identify root causes and implement corrective actions. This position requires a proactive approach to quality management and a commitment to upholding industry standards. Your expertise will be instrumental in ensuring the integrity and safety of our pharmaceutical products. If you are a detail-oriented QA professional with a passion for quality and a desire to contribute to a leading pharmaceutical organization, we encourage you to apply.
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Pharmaceutical Quality Assurance Specialist
55000 Hoa Sơn
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Job Description
Our client is seeking a detail-oriented and experienced Pharmaceutical Quality Assurance Specialist to join their dynamic team in Da Nang, Da Nang, VN . This role is essential for ensuring that our client's pharmaceutical products meet the highest standards of quality, safety, and efficacy, adhering to all regulatory requirements. The Quality Assurance Specialist will be responsible for developing, implementing, and maintaining the quality management system, conducting internal audits, reviewing batch records, investigating deviations and out-of-specification (OOS) results, and managing change control processes. Key responsibilities include ensuring compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant industry regulations; participating in regulatory inspections and audits; reviewing and approving quality-related documentation; collaborating with manufacturing, R&D, and regulatory affairs departments to resolve quality issues; and contributing to the continuous improvement of quality processes. The ideal candidate will possess a strong understanding of pharmaceutical manufacturing processes, quality control principles, and regulatory affairs. Excellent analytical, problem-solving, and documentation skills are crucial. This position offers a hybrid work arrangement, providing flexibility while maintaining essential on-site collaboration. If you are a dedicated quality professional passionate about ensuring the integrity of pharmaceutical products and contributing to public health, we encourage you to apply.
Responsibilities:
Responsibilities:
- Implement and maintain the Quality Management System (QMS) according to pharmaceutical regulations.
- Conduct internal audits and ensure compliance with GMP and GLP.
- Review and approve batch records, validation reports, and other quality documents.
- Investigate deviations, OOS results, and customer complaints.
- Manage the change control process and ensure proper implementation.
- Participate in external audits and regulatory inspections.
- Collaborate with cross-functional teams to address quality issues.
- Contribute to the continuous improvement of quality processes and systems.
- Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science field.
- Minimum of 3-5 years of experience in Quality Assurance within the pharmaceutical industry.
- In-depth knowledge of GMP, GLP, and other relevant regulatory guidelines (e.g., FDA, EMA).
- Experience with quality control testing and data analysis.
- Strong understanding of pharmaceutical manufacturing processes.
- Excellent documentation, analytical, and problem-solving skills.
- Proficiency in quality management software is a plus.
- Ability to work effectively in a hybrid work environment.
This advertiser has chosen not to accept applicants from your region.
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Pharmaceutical Quality Assurance Specialist
07000 Nam Dinh , Nam Dinh
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Job Description
Our client is seeking a meticulous and experienced Pharmaceutical Quality Assurance Specialist to join their remote team. This critical role ensures that all pharmaceutical products meet stringent quality standards and comply with regulatory requirements throughout the development and manufacturing lifecycle. You will be responsible for developing and implementing quality management systems, conducting internal audits, reviewing batch records, and investigating deviations and out-of-specification results. Your ability to maintain meticulous documentation, interpret regulatory guidelines (e.g., GMP, FDA), and collaborate effectively with cross-functional teams (e.g., R&D, Manufacturing, Regulatory Affairs) will be essential. We are looking for individuals with a strong background in pharmaceuticals or biotechnology, excellent analytical skills, and a deep understanding of quality assurance principles. Proficiency with quality management software and a commitment to continuous improvement are highly desirable. This is an exciting opportunity to contribute to the integrity and safety of life-saving medications from a remote work setup. The ideal candidate will be detail-oriented, possess strong problem-solving skills, and have excellent written and verbal communication abilities. You should be comfortable working independently and managing multiple QA-related tasks with precision. Your role will be pivotal in ensuring product quality and compliance, thereby safeguarding patient health and supporting our client's reputation for excellence.
Responsibilities:
Qualifications:
Responsibilities:
- Implement and maintain the Quality Management System (QMS) in compliance with GMP and other relevant regulations.
- Conduct internal audits of manufacturing processes, documentation, and systems.
- Review and approve batch records, analytical data, and validation reports.
- Investigate deviations, out-of-specification results, and customer complaints.
- Develop and implement corrective and preventive actions (CAPAs).
- Participate in external audits and regulatory inspections.
- Provide training to personnel on quality assurance principles and procedures.
- Collaborate with manufacturing and R&D teams to resolve quality issues.
- Monitor and analyze quality metrics to identify trends and areas for improvement.
- Stay updated with evolving pharmaceutical quality standards and regulatory requirements.
Qualifications:
- Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science field.
- Minimum of 3-5 years of experience in pharmaceutical quality assurance or quality control.
- Thorough understanding of Good Manufacturing Practices (GMP) and other relevant regulatory guidelines.
- Experience with internal audits, batch record review, and deviation investigations.
- Proficiency in quality management software and tools.
- Strong analytical and problem-solving skills.
- Excellent written and verbal communication skills.
- Ability to work independently and manage multiple priorities in a remote setting.
- Detail-oriented with a strong commitment to quality and compliance.
This advertiser has chosen not to accept applicants from your region.
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Pharmaceutical Quality Assurance Specialist
710000 My Tho, Tien Giang
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Job Description
Our client is seeking a meticulous and experienced Pharmaceutical Quality Assurance Specialist to uphold the highest standards of product quality and compliance. This role involves a hybrid work arrangement, allowing for strategic collaboration in the office and focused remote work. As a Quality Assurance Specialist, you will be responsible for developing, implementing, and maintaining quality systems and procedures throughout the pharmaceutical product lifecycle. You will ensure adherence to Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant regulatory guidelines.
Key responsibilities include reviewing and approving batch records, conducting internal audits, and managing deviations, CAPAs (Corrective and Preventive Actions), and change controls. You will also participate in vendor qualification processes, analyze quality data, and contribute to the continuous improvement of quality processes. The ideal candidate will have a strong understanding of pharmaceutical manufacturing, regulatory affairs, and quality management systems. Excellent analytical, problem-solving, and documentation skills are essential.
You will collaborate closely with cross-functional teams, including R&D, production, and regulatory affairs, to ensure product quality and compliance. This role requires a proactive approach to identifying and mitigating quality risks. Strong communication skills are necessary for interacting with internal stakeholders and potentially external regulatory bodies. If you are a detail-oriented professional with a passion for ensuring pharmaceutical product integrity and safety, we encourage you to apply.
Responsibilities:
Key responsibilities include reviewing and approving batch records, conducting internal audits, and managing deviations, CAPAs (Corrective and Preventive Actions), and change controls. You will also participate in vendor qualification processes, analyze quality data, and contribute to the continuous improvement of quality processes. The ideal candidate will have a strong understanding of pharmaceutical manufacturing, regulatory affairs, and quality management systems. Excellent analytical, problem-solving, and documentation skills are essential.
You will collaborate closely with cross-functional teams, including R&D, production, and regulatory affairs, to ensure product quality and compliance. This role requires a proactive approach to identifying and mitigating quality risks. Strong communication skills are necessary for interacting with internal stakeholders and potentially external regulatory bodies. If you are a detail-oriented professional with a passion for ensuring pharmaceutical product integrity and safety, we encourage you to apply.
Responsibilities:
- Ensure compliance with cGMP, ICH, and other relevant pharmaceutical regulations.
- Review and approve manufacturing and laboratory batch records for accuracy and completeness.
- Manage deviations, OOS (Out-of-Specification) investigations, and CAPA implementation.
- Conduct internal audits and support external regulatory inspections.
- Participate in change control processes to evaluate and implement modifications to processes and documentation.
- Develop and update quality procedures, work instructions, and specifications.
- Analyze quality metrics and trends to identify areas for continuous improvement.
- Collaborate with production, QC, and other departments to resolve quality issues.
- Contribute to product lifecycle management and regulatory submissions.
This advertiser has chosen not to accept applicants from your region.
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