1 746 Quality Lead jobs in Vietnam

About Dat Bike

Dat Bike 

is a technology startup whose mission is to drive mass adoption of green transportation in Vietnam. We make the most compelling and dependable electric bikes so that customers can just switch without making any compromises. To do this, we welcome the brightest people to join our journey.

About Job

Quality Lead (IQC/SQC) is responsible for driving suppliers quality initiatives and activities, including quality plan implementation, guiding selected suppliers through the approval and qualification processes and training suppliers on quality requirements, driving continuous improvement, do suppliers auditing to ensure compliance with Dat Bike requirements.

Responsibilities

• To chair the meeting with suppliers to settle all Technical materials/parts/components issues.
• New suppliers qualification base on Dat Bike's requirement.
• Suppliers annual audit and publish the audit check list accordingly and follow up the suppliers improvement action plan after auditing.
• Perform onsite supplier visit for root cause analysis and verification of CAPA report of suppliers quality issues, work with suppliers to close out any open CAPA in a timely.
• Work with PD and RD team to define process parameters and criteria to ensure supplier process capability is effective to meet products and process requirements.
• Provide expertise in supplier development initiatives to ensure best practice and industry standards are implemented and operated at all suppliers.
• Train suppliers on the company system/requirements and monitor suppliers activities for non-conformance.
• Lead supplier approval process by assessing potential new suppliers' manufacturing capabilities.
• Oversee new safe products launch, leading activities such control plan, first inspection…
• Issue the Non-conformance and suppliers CAPA log sheet to follow up all suppliers improvement action which are committed by suppliers.
• Make suppliers claims log sheets report to follow up all suppliers compensation.

Requirements

• Bachelor's degree in Mechanical, Electrical, Electronics, Mechatronics Engineering or related field.
• Minimum of 3-5 years of experience in manufacturing quality management roles, preferably in the automotive or related industry.
• Knowledge of quality management principles, methodologies, and tools(FMEA, SPC, CAPA, PDCA, 8D Analysis, 7 QC Tools, TQM, Keizen.
• Proven experience in leading teams and driving continuous improvement initiatives.
• Excellent communication, leadership, and problem-solving skills
• Good at English

Benefits

• Competitive income.
• Meal support according to company policy
• Social insurance.
• MIC insurance.
• Discount price to buy a Dat Bike.

Location

Dat Bike factory, No.1 CN10, Tan Binh, Tay Thanh, Tan Phu District, Ho Chi Minh City

Mô tả công việc

• Chịu trách nhiệm lập kế hoạch, thiết kế và thực hiện kiểm thử phần mềm.
• Xây dựng, quản lý và cải tiến quy trình QA nhằm đảm bảo chất lượng sản phẩm.
• Quản lý, đào tạo và hỗ trợ các thành viên QA trong nhóm.
• Phối hợp chặt chẽ với các bộ phận phát triển, BA, PM để kiểm soát chất lượng trong suốt vòng đời dự án.
• Báo cáo tiến độ, kết quả test và đề xuất các biện pháp cải thiện chất lượng sản phẩm.

Yêu cầu

• Có kinh nghiệm vững trong thiết kế test case, thực hiện test và quản lý quy trình kiểm thử.
• Có khả năng
  tự chủ trong việc thiết kế và thực hiện test
  .
• Trình độ tiếng Nhật
  N3 trở lên
  .
• Trình độ tiếng Anh
  TOEIC 800+
  hoặc tương đương (business level).
• Có kỹ năng lãnh đạo, quản lý nhóm và giao tiếp tốt.
• Ưu tiên ứng viên có chứng chỉ
  ISTQB
  .

Quyền lợi

• Lương hấp dẫn
  (thương lượng theo năng lực).
• Xét tăng lương định kỳ
  theo hiệu suất.
• Đóng đầy đủ
  bảo hiểm
  theo quy định pháp luật Việt Nam.
• Thưởng hiệu suất, thưởng dự án
  theo kết quả triển khai.
• 12 ngày phép/năm
  , nghỉ lễ theo quy định Nhà nước.
• Khám sức khỏe định kỳ
  hằng năm.
• Môi trường làm việc
  ổn định, thân thiện, theo phong cách Nhật Bản
  .
• Hỗ trợ
  team building, nghỉ mát, quà sinh nhật và các hoạt động nội bộ
  định kỳ.

Company:
An IT product company specializing in systems that analyze and connect data across engineering and supply chains for the manufacturing industry.

Location:
Hybrid in Binh Thanh (work in the office once per week)

Salary:
FROM
$3,000

Responsibilities

• You'll lead the definition and execution of our product QA strategy. Your mission is to continuously deliver value and earn customer trust. You'll achieve this by collaborating and discussing with stakeholders from a broad perspective, moving beyond just "how to ensure quality and improve processes" to also consider "why quality is important and what we should prioritize right now".

• You will be responsible for establishing the first QA team in the Vietnamese organization from scratch.

Qualifications

• 7+ years of experience in similar positions

• Experience leading the formulation and execution of QA strategies

• Experience playing a central role in improving quality in a rapidly growing product

• Fluent business communication skills in English.

• Experience in development and QA for large-scale systems spanning multiple teams

• Experience in designing test processes following standards such as ISTQB and ISO29119, and general QA practices, and implementing them in development organizations

Benefits

• Annual paid leave: 12 days

• Year-end holidays (December 31 to January 2)

• Salary review twice a year

• Employee Stock Option

• 13th-month salary

• Salary review: every 6 months

• 100% monthly basic salary and mandatory social insurances for a 2-month probation period

• Premium Health Insurance

• Social insurance, health insurance, unemployment insurance, workers' accident compensation insurance

• Annual health check-up

• Intensive training program (external or internal training courses, workshop, etc)

• Devices: PC and display of desired specifications

• Company awards, every 6 month-MVP-award

• Year-end party, team building, etc

Interview process:

1st: HR Interview or Online English speaking test

2nd: Technical assignment (work sample)

3rd: Technical interview with engineers

4th: Final interview with CTO

• Lead the development, implementation, and continuous improvement of the Quality Management System (QMS) in alignment with global regulatory standards (e.g., FDA, EMA, WHO).
• Oversee and manage all aspects of pharmaceutical quality assurance, including batch record review, deviation investigation, CAPA management, change control, and validation.
• Ensure compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and Good Distribution Practices (GDP).
• Conduct internal audits and support external regulatory inspections, ensuring readiness and successful outcomes.
• Develop and implement quality training programs for personnel involved in pharmaceutical manufacturing and development.
• Collaborate with R&D, manufacturing, and regulatory affairs teams to ensure quality is integrated into product development and commercialization.
• Analyze quality data, identify trends, and implement preventive actions to mitigate risks.
• Manage and mentor a team of quality assurance professionals, fostering a culture of quality excellence.
• Stay current with evolving pharmaceutical regulations and industry best practices.
• Serve as a key point of contact for quality-related inquiries and issues.

• Master's or Ph.D. in Pharmacy, Pharmaceutical Sciences, Chemistry, Biology, or a related discipline.
• A minimum of 10 years of progressive experience in pharmaceutical quality assurance and quality control, with at least 4 years in a leadership or principal role.
• Deep understanding of pharmaceutical manufacturing processes, drug development, and regulatory affairs.
• Extensive knowledge of global pharmaceutical regulations, including ICH guidelines, FDA CFR, and EU GMP.
• Proven experience in leading successful regulatory inspections and audits.
• Exceptional analytical, problem-solving, and decision-making skills.
• Outstanding leadership, communication, and interpersonal skills, with the ability to effectively manage and mentor teams remotely.
• Proficiency in QMS software and data analysis tools.
• Experience in sterile manufacturing, biologics, or specific therapeutic areas is a strong asset.
• Demonstrated ability to drive quality initiatives and ensure compliance in complex organizations.

• Lead and manage the Quality Assurance department, including team supervision and development.
• Develop, implement, and maintain the company's Quality Management System (QMS).
• Ensure compliance with all relevant pharmaceutical regulations and GMP guidelines.
• Conduct internal audits of manufacturing processes, facilities, and documentation.
• Oversee the investigation of deviations, customer complaints, and out-of-specification results.
• Manage Corrective and Preventive Actions (CAPA) programs.
• Review and approve batch records, validation protocols, and other quality-related documents.
• Collaborate with production and other departments to resolve quality issues.
• Participate in regulatory inspections and audits by health authorities.
• Drive continuous improvement initiatives to enhance product quality and process efficiency.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
• Minimum of 5-7 years of experience in Quality Assurance within the pharmaceutical industry.
• In-depth knowledge of GMP, ICH guidelines, and other relevant regulatory standards.
• Proven experience in leading QA teams and managing QMS.
• Strong understanding of pharmaceutical manufacturing processes.
• Excellent auditing, investigation, and problem-solving skills.
• Proficiency in documentation review and approval.
• Strong leadership, communication, and interpersonal skills.
• Ability to work effectively with cross-functional teams.

• Lead and manage the automotive quality assurance team and processes.
• Develop, implement, and maintain the company's quality management system (QMS).
• Establish and enforce quality control standards and procedures for manufacturing.
• Conduct regular quality audits of production lines, components, and finished vehicles.
• Investigate quality issues, perform root cause analysis, and implement corrective actions (CAPA).
• Collaborate with Engineering, Production, and Supply Chain teams to ensure product quality.
• Monitor key quality metrics and report on performance to senior management.
• Train and mentor QA personnel, fostering a culture of quality excellence.
• Ensure compliance with industry-specific quality standards (e.g., IATF 16949).
• Drive continuous improvement initiatives to enhance product quality and manufacturing efficiency.

• Bachelor's degree in Engineering (Mechanical, Electrical, or related field), or equivalent practical experience.
• 7+ years of experience in quality assurance within the automotive industry.
• Proven experience in a leadership or supervisory role within a QA department.
• In-depth knowledge of IATF 16949 standards and automotive quality principles.
• Experience with quality tools and methodologies (e.g., FMEA, SPC, 8D).
• Strong analytical, problem-solving, and decision-making skills.
• Excellent communication, interpersonal, and leadership abilities.
• Proficiency in quality management software and MS Office Suite.
• Ability to work effectively in a manufacturing environment.

• Develop, implement, and manage comprehensive quality assurance programs for pharmaceutical products.
• Ensure compliance with cGMP, GLP, GCP, and other relevant regulatory guidelines.
• Conduct internal audits and inspections to assess compliance and identify areas for improvement.
• Manage deviations, CAPAs (Corrective and Preventive Actions), and change control processes.
• Review and approve quality-related documentation, including SOPs, batch records, and validation reports.
• Provide training and guidance to personnel on quality assurance principles and regulatory requirements.
• Lead and mentor QA team members.
• Liaise with regulatory agencies during inspections and inquiries.
• Analyze quality data and metrics to identify trends and implement corrective actions.
• Contribute to the development and improvement of the company's Quality Management System (QMS).

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life sciences field.
• Minimum of 8 years of progressive experience in pharmaceutical Quality Assurance or Quality Control.
• In-depth knowledge of global pharmaceutical regulations (e.g., FDA, EMA, ICH guidelines).
• Proven experience in developing and implementing QA systems and procedures.
• Strong understanding of manufacturing processes, analytical testing, and clinical trial operations.
• Excellent auditing, problem-solving, and decision-making skills.
• Exceptional written and verbal communication and interpersonal skills.
• Ability to manage multiple priorities and work effectively in a remote, independent environment.
• Experience with QMS software and electronic batch records is a plus.
• Detail-oriented with a commitment to accuracy and compliance.