1 321 Quality Systems jobs in Vietnam
Manager, Quality Systems
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At STERIS, we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe.
Position Summary
The Quality Manager is responsible for leading quality improvement for an AST processing or lab facility. This position leads implementing and maintaining state-of-the-art quality practices and assumes overall responsibility in ensuring that the site maintains operational and quality systems in a state of compliance to domestic and international standards.
The role is responsible for the organization, documentation, and maintenance of the quality system to be compliant with, as appropriate, the following standards: ISO 9001, ISO 13485, FDA 21 CFR Part 820/211, EU GMPs, ISO 17025, ISO 11137 and/or ISO 11135 and other applicable regulatory standards. This role leads the local site efforts focused on quality system improvement, supplier quality, process quality, new service/modality/technology development quality and quality system compliance. The Quality Manager serves as the Management Representative for the site(s) and is responsible for ensuring the quality system meets all applicable regulatory standards.
The Quality Manager has the responsibility, duty, and decision-making authority to put any product on hold that is identified as potentially non-conforming and escalating as needed for additional reviews by Technical teams.
Parque Zona Franca Las Americas
Santo Domingo Este, Republica Dominicana
Location STERIS DR is
What You'll Do As a Manager Quality Systems
- Lead the organization's Quality staff to ensure compliance to the overall Quality Management System and drive continuous improvement.
- Lead the organization's Quality staff to ensure alignment to operations, support Lean efforts and drive quality improvement for services/processes.
- Work closely with site senior management to provide strategic direction and development of the organization's quality strategies and tactics.
- Provide quality viewpoints and opinions on future service/technology offerings.
- Provide coaching, mentoring and leadership to the Quality staff.
- Serve as the site's Management Representative and lead the organization's Management Review process.
- Ensure compliance with appropriate domestic regulatory and international standards and requirements.
- Lead the organization's continuous improvement process; including data analysis, improvement projects and process capability to improve key metrics as measured by the product/service quality dashboard.
- Lead and implement effective production and process controls.
- Manage the CAPA, complaint and non-conformance handling processes to ensure customer responsiveness and process improvements.
- Responsible for successfully leading and managing Regulatory Agency and Notified Body inspections and driving the creation and implementation of sustainable and effective remediation plans. Responsible for overseeing completion of Customer audits.
- Apply regulatory knowledge and judgment to the evaluation of quality concerns and regulatory compliance issues.
- Travel to other AST facilities, domestically and/or globally, to support remediation activities, audits/inspections, and/or continuous improvement initiatives.
- Overall responsibilities include commitment to ensure external and internal requirements are met according to documented policies, procedures, standards, and regulations.
- The position requires a level of authority to conduct and direct required activities such as quality planning, personnel management, and regulatory compliance.
- Perform other duties as assigned.
The Experience, Skills, And Abilities Needed
Required:
- Graduate/Masters (related scientific or technical degree)
- Minimum 10 years of combined Manufacturing/Quality Engineering and/or Quality Systems experience
- Minimum 10 years of experience working in an ISO certified environment
- Minimum of 2 years in a Quality leadership role
- Excellent problem-solving skills
- Focus on identification of potential issues and continuous improvement
- Experience working on cross-functional teams and on own initiative
- Must have PC experience, as well as working familiarity of desktop applications including Excel, Word, and PowerPoint
- Bilingual English/Spanish
Preferred:
- Sterilization experience
- Working knowledge of FDA QSR/ EUGMP regulations
- Minimum 10 years of experience with medical device or other regulated industries
Other:
- Ability to work in a fast-paced, regulated environment with strict deadlines and ever-changing responsibilities
- Mathematical skills including practical application of fractions, percentages, ratios, proportions, and algebra
- Effective interpersonal skills, ability to work independently under minimal guidelines and supervision
- Demonstrated excellent organizational, oral, and written communications skills
STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention. WE HELP OUR CUSTOMERS CREATE A HEALTHIER AND SAFER WORLD by providing innovative healthcare, life sciences and dental products and services. STERIS is a $5 billion, publicly traded (NYSE: STE) company with approximately 17,000 associates and Customers in more than 100 countries.
STERIS strives to be an Equal Opportunity Employer.
Quality Management Assistant Manager
Posted today
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Job Description
Are you a
Quality Management Assistant Manager
passionate about quality management? If so, this opportunity could be for you Join us in Hanoi at B. Braun, a leader in the medical devices industry, where your skills and experience will be recognized and celebrated. Take the next step in your career with us and help shape the future of healthcare
As a
Quality Management Assistant Manager
at B. Braun, you will play a vital role in administering quality management system of the assigned production facilities.
Main job responsibilities:
- Assist QM Manger to ensure establishment and maintenance of the quality management system to meet WHO GMP, ISO as well as other regulatory and company requirements, include lead responsible for reviewing & revising QM documents.
- Properly apply production and operation controls to meet GMP, ISO and related regulatory requirements.
- Control and monitor the quality performance objective.
- Establish and lead the annual audit program (internal, external and division…) including unplanned audit and inspection.
- Coordinate and follow up the CAPA, Customer Complaints, Audits, Change Control, Risk Management with relevant stakeholders to ensure all matters are solved properly and in accordance with requirements, verify improvement actions and evidence.
- Prepare quality reports and any information that required.
- Act as local safety officer to execute properly relevant SOPs for this responsibility including Recall, HHA, Vigilance.
- Evaluate, assessment and give final QM statement for IC & PC complaints on SAP C3, and DIR, CAPA… on B.TraQS
- Coordinate with relevant stakeholders to ensure the technical registration of BBVN at oversea market to be provided properly and on time in full.
- Supervise, develop team members and provide the on-the-job coach and guidance.
Qualification Requirements:
- Bachelor degree in technical or pharmacy field
- More than 6 years of related working experience in quality management in manufacturing environment, medical devices/ pharmaceutical industry preferred
- Experience in leading a team
- Standard: ISO 9001, ISO 19011, ISO 14644, GMP ; 5whys analysis
- Good English and communication skill
- Auditting, reporting, presentation, troubleshooting skill
What sets B. Braun apart?
B. Braun Vietnam, a subsidiary of one of the world's leading healthcare technology companies, B. Braun Melsungen AG Group, now operates one of the largest medical complexes in Vietnam and has become a prestigious trademark in Vietnam healthcare market. With more than 1,400 employees nationwide and proud to be one of 'Best Companies to Work for' in Asia, we develop high quality "made in Vietnam" products widely being used and appreciated in international and domestic market. Our product offering ranges from hospital consumables to high-tech medical devices and equipment.
Every service provided by B. Braun Vietnam incorporates the entirety of our knowledge and skills, the company's deep understanding of users' needs and extensive expertise. Our mission is to PROTECT and IMPROVE the health of people around the world. We welcome you to join the B. Braun family and share your expertise
What can we offer you?
- Competitive salary and attractive annual bonus
- Guaranteed 13th month salary
- Company health insurance
- Responsibility allowance
- Service award
- Company canteen or lunch allowance
- Company bus for those based in Hanoi Plant
- Exciting company engagement activities
What's next?
Upon receiving your application, our dedicated Talent Acquisition team will review your application. If you stand out, you'll be invited to engage in dynamic interviews, ranging from phone calls to video chats and in-person meetings. Throughout this process, we will keep you informed and inspired with regular updates and feedback. Finally, if you shine through and decide to join us, we will lead you into our seamless onboarding experience. Join us and be part of something extraordinary
We appreciate different perspectives, thoughts, experiences and backgrounds. By strengthening an appreciative, inclusive, respectful and equal working environment, we create a culture in which all our employees feel free to be who they are. To find out more about our commitment to diversity click here
Check us out on Social Media
B. Braun Group LinkedIn
B. Braun Group YouTube
To find out more about B. Braun Vietnam just click here
Total Quality Management Intern
Posted today
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Job Description
JOB DESCRIPTION
Responsible for data quality and using data analysis tool/others method to detect any abnormal data that may potentially impact data quality
Manage project from start to end: Briefing, monitor data quality, propose action for abnormal data or data quality issue
Brief project requirement to Audio checker to ensure understanding project requirements
Repair project report to stakeholders and Report to line manager
Other Task/initiative assigned by line Manager
REQUIREMENTS
Fresh graduates or 4th year students who can work full-time;
Strong communication skills, ability to present the findings in a detailed and accurate manner;
Proficiency use of Microsoft office, especially Excel;
Having knowledge of Programming, Macro,. is a plus point
Detail-oriented, both in understanding instructions and executing process and deliverables;
Organized with strong time management skills;
Logical thinking;
Good English communication is a plus.
Workplace:
Level 4, Centre Point Building, No. 106, Nguyen Van Troi Street, Ward 8, Phu Nhuan District, Ho Chi Minh city
Working hours:
From 9:00 to 18:00 (Mon - Fri), Lunch break: 1 hour
BENEFITS
Salary: 6,000,000 VND/month
Dynamic and creative working environment at the world's leading multinational cooperation in the market research industry
Comprehensive self-development with intensive training programs and follow-up by a senior manager
Enjoy the welfare policies in accordance with the company's regulations.
HOW TO APPLY
Kindly submit your English CV to Ms. Nhi ) with subject: (NielsenIQ - CMI Ops) - (TQM Checker) – (Your Full Name)
Head of Quality Management
Posted today
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Job Description
JOB TITLE:
Head of Quality Management – Carmel International Hospital
Location:
Ho Chi Minh City, Vietnam
Reports to:
Chief Executive Officer (CEO) – Carmel International Hospital
JOB SUMMARY:
The Head of Quality Management is responsible for leading the hospital-wide quality assurance and patient safety programs, with a strategic focus on achieving Joint Commission International (JCI) accreditation. This role oversees the planning, implementation, monitoring, and evaluation of quality initiatives, ensuring that clinical and operational practices align with international best practices, regulatory standards, and Carmel International Hospital's mission of delivering world-class healthcare.
The Head of Quality Management collaborates with clinical, administrative, and support service leaders to foster a culture of continuous improvement, patient-centered care, risk management, and regulatory compliance.
KEY RESPONSIBILITIES:
Quality Leadership & Governance
- Lead the hospital's quality and patient safety strategy, including the development and implementation of a hospital-wide Quality Management System (QMS).
- Establish and chair the hospital's Quality Council and relevant sub-committees (e.g., Patient Safety, Infection Control, Risk Management).
- Serve as the primary advisor to executive leadership on all quality-related matters, including accreditation readiness, regulatory compliance, and quality performance.
- Foster a culture of continuous quality improvement, safety, and accountability across all departments.
- Ensure compliance with local, national, and international regulations, including those from the Ministry of Health, Department of Health, and other accreditation bodies.
- Lead the hospital's preparation for JCI accreditation including gap analyses, policy development, and staff readiness.
Performance Improvement & Data Management
- Design and oversee the hospital's Performance Improvement Program, including identification of key KPIs, benchmarking, and dashboard reporting.
- Utilize data analytics and root cause analysis tools (e.g., RCA, FMEA) to drive evidence-based improvements in clinical and operational outcomes.
- Coordinate hospital-wide quality improvement projects in collaboration with departmental leaders.
- Monitor quality metrics and publish regular performance reports for leadership review and decision-making.
Risk Management & Patient Safety
- Develop and implement an effective Risk Management Program to identify, assess, and mitigate clinical and operational risks.
- Lead incident reporting systems, adverse event reviews, and investigations of sentinel events or near-misses.
- Promote a "Just Culture" that encourages transparent reporting and learning from errors without blame.
- Ensure effective operation of patient safety programs, including hand hygiene, medication safety, fall prevention, and infection control.
Policy Development & Document Control
- Oversee the development, approval, implementation, and review of hospital-wide policies, procedures, and SOPs in line with JCI standards.
- Establish and maintain a centralized Document Control System to ensure policy accessibility, version control, and compliance.
- Collaborate with department heads to ensure departmental policies align with overall hospital quality standards.
Training & Staff Engagement
- Organize hospital-wide training programs on quality management, patient safety, accreditation, and performance improvement.
- Conduct orientation sessions for new staff on hospital quality goals, expectations, and standards.
- Provide coaching, mentorship, and professional development opportunities for the Quality Management team.
- Encourage cross-departmental collaboration and staff engagement in quality initiatives.
Internal Audits & Continuous Monitoring
- Plan and lead regular internal audits, clinical practice evaluations, and compliance reviews across all departments.
- Track audit findings and support departments in implementing corrective and preventive actions (CAPA).
- Report audit results to hospital leadership and accreditation bodies as required.
- Maintain a readiness state for unannounced surveys or inspections.
QUALIFICATIONS & EXPERIENCE:
Education & Certifications
- Bachelor's degree in Healthcare Administration, Public Health, Quality Management, or a related clinical field.
- Professional certification in healthcare quality or patient safety (e.g., CPHQ, CPPS, JCI Internal Surveyor, Six Sigma) is highly desirable.
Experience
- Minimum 8–10 years of experience in healthcare quality management, patient safety, or hospital accreditation.
- At least 5 years in a senior leadership or department head role, preferably in a JCI-accredited hospital.
- Demonstrated success in leading hospital-wide quality initiatives and accreditation processes.
- In-depth knowledge of JCI standards, MoH regulations, ISO 15189, and international healthcare quality frameworks.
- Strong understanding of clinical workflows, risk management principles, infection control, and performance improvement tools.
Senior Quality Assurance Manager - ISO Standards
Posted 8 days ago
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Job Description
Key Responsibilities:
- Develop, implement, and maintain the company's Quality Management System (QMS).
- Lead and mentor the Quality Assurance team, providing guidance and setting performance objectives.
- Conduct regular internal audits to assess compliance with ISO standards and internal procedures.
- Manage and oversee the process for handling customer complaints and non-conformances.
- Implement and manage Corrective and Preventive Actions (CAPA) system.
- Ensure that all products and processes meet defined quality standards and regulatory requirements.
- Collaborate with R&D, production, and other departments to integrate quality considerations into all stages of product development and manufacturing.
- Prepare for and facilitate external audits by certification bodies and regulatory agencies.
- Analyze quality data to identify trends, root causes of issues, and areas for improvement.
- Develop and deliver quality training programs to employees.
- Stay up-to-date with relevant quality standards, regulations, and best practices.
- Drive continuous improvement initiatives within the quality function and across the organization.
- Bachelor's degree in Engineering, Science, or a related technical field. Master's degree is a plus.
- Minimum of 7 years of progressive experience in Quality Assurance or Quality Control roles.
- Proven experience in implementing and managing ISO 9001 or other relevant quality management systems.
- Experience conducting internal and external audits.
- Strong knowledge of quality tools and methodologies (e.g., Six Sigma, Lean, SPC).
- Excellent analytical, problem-solving, and root cause analysis skills.
- Proficiency in quality management software and data analysis tools.
- Exceptional leadership, communication, and interpersonal skills.
- Ability to manage multiple priorities and work effectively in a hybrid environment.
- Detail-oriented with a commitment to accuracy and compliance.
Engineer - Quality Management (Risk analysis)
Posted today
Job Viewed
Job Description
Are you an Engineer - Quality Management passionate about quality management? If so, this opportunity could be for you Join us in Hanoi at B. Braun, a leader in the medical devices industry, where your skills and experience will be recognized and celebrated. Take the next step in your career with us and help shape the future of healthcare
As an Engineer - Quality Management at B. Braun you will play a vital role in leading risk assessment activity for medical plants
Your key responsibilities:
- Lead risk assessment activity for medical plants: Take lead risk assessment activity from QM.
- Respond to create, supervise, and manage the risk assessment management file of medical plant.
- Respond to lead team to involve and do risk assessment of change controls, improvement projects and projects to meet requirements with stakeholders
- Coordinate with stakeholders to executive the risk assessment management file.
- To create/revise the risk assessment documentations shall comply with ISO standards, Global documentations
- Validation activity: Input risk analysis for Validation engineer during prepare validation. Update risk analysis after validation activities
- Project activity: Coordinate with Regional and Global to executive the risk assessment projects, programs. Involve/perform relate tasks to risk analysis as risk assessment expert
- Create/revise/ Training SOP Risk analysis
What you will bring to the team:
- Bachelor's Degree with 2 years of related working experience or Master's degree with 1 year of related working experience in risk management
- Requires working knowledge of technical or production field.
- Knowlegle in ISO 13485, ISO 9001, ISO 14971 is preferred
- Knowledge of root cause analysis or 5 whys analysis. Have experienct about FMEA method/ 5M + 1E during control deviation in production is preferred
- Good English
- Communication. MS Office. Presentation. Team work
What sets B. Braun apart?
B. Braun Vietnam, a subsidiary of one of the world's leading healthcare technology companies, B. Braun Melsungen AG Group, now operates one of the largest medical complexes in Vietnam and has become a prestigious trademark in Vietnam healthcare market. With more than 1,400 employees nationwide and proud to be one of 'Best Companies to Work for' in Asia, we develop high quality "made in Vietnam" products widely being used and appreciated in international and domestic market. Our product offering ranges from hospital consumables to high-tech medical devices and equipment.
Every service provided by B. Braun Vietnam incorporates the entirety of our knowledge and skills, the company's deep understanding of users' needs and extensive expertise. Our mission is to PROTECT and IMPROVE the health of people around the world. We welcome you to join the B. Braun family and share your expertise
What can we offer you?
- Competitive salary and attractive annual bonus
- Guaranteed 13th month salary
- Company health insurance
- Responsibility allowance
- Service award
- Company canteen or lunch allowance
- Company bus for those based in Hanoi Plant (to be included for those working in Plant)
- Exciting company engagement activities
What's next?
Upon receiving your application, our dedicated Talent Acquisition team will review your application. If you stand out, you'll be invited to engage in dynamic interviews, ranging from phone calls to video chats and in-person meetings. Throughout this process, we will keep you informed and inspired with regular updates and feedback. Finally, if you shine through and decide to join us, we will lead you into our seamless onboarding experience. Join us and be part of something extraordinary
We appreciate different perspectives, thoughts, experiences and backgrounds. By strengthening an appreciative, inclusive, respectful and equal working environment, we create a culture in which all our employees feel free to be who they are. To find out more about our commitment to diversity click here
Check us out on Social Media
B. Braun Group LinkedIn
B. Braun Group YouTube
To find out more about B. Braun Vietnam just click here
Listing & Content Quality Management - Operations,
Posted today
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Job Description
Job Description
Process Optimization & Automation
- Simplify workflows and improve efficiency through process automation using tools like MS Excel (e.g., Pivot, VLOOKUP).
- Monitor and optimize cost metrics, such as cost per task and cost per 1K orders.
- Stay ahead of industry standards and leverage user feedback to optimize features and strategies.
Policy Implementation & Process Improvement
- Implement and refine policies to improve listing quality, reduce violations, and enhance detection accuracy.
- Stay ahead of industry standards and leverage user feedback to optimize features and strategies.
BPO Management
- Manage external BPO teams to ensure performance meets SLA, task coverage, and backlog clearance goals.
- Drive agent productivity and optimize task allocation through efficient processes.
Quality Control & Risk Management
- Develop internal controls to reduce violations, manage bans/deletions, and ensure compliance with policies.
- Identify and anticipate risks in policy execution and proactively address gaps.
Data Analysis & Performance Optimization
- Analyze performance metrics (e.g., fail rate, trigger rate, violation patterns) and propose solutions for improvement.
- Use data insights to optimize policies, processes, and operational performance.
Key Metrics to Drive
- Performance: SLA, task coverage, backlog clearance, agent productivity, and detection accuracy.
- Cost: Optimize operational costs, including the cost per task and cost per order.
- Quality: Fail rate, trigger rate, leakage, violation reduction, and adherence to QC standards.
Requirements
- At least 2-3 years of experience in e-commerce operations, focusing on product/content quality control and compliance management.
- Strong understanding of how QC impacts other business teams, with the ability to support feature launches, campaigns, and project control at all stages.
- Logical and optimization thinking with the ability to anticipate risks in policy and execution.
- Analytical skills to solve problems and propose data-driven improvements.
- Proficiency in MS tools (e.g., Pivot, VLOOKUP) for data analysis and reporting.
- Detail-oriented, responsible, and adaptable to changing priorities.
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Agency Distribution Sales Quality Management Manager
Posted today
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Job Description
Prudential's purpose is to be partners for every life and protectors for every future. Our purpose encourages everything we do by creating a culture in which diversity is celebrated and inclusion assured, for our people, customers, and partners. We provide a platform for our people to do their best work and make an impact to the business, and we support our people's career ambitions. We pledge to make Prudential a place where you can Connect, Grow, and Succeed.
This job holder will play crucial role in building a risk and control culture for Agency channel via risk control assignments from PCA and PVA assignment. The job holder is also in charge of risk and control sharing sessions, perform data analysis to monitor sales quality indicators, assess internal controls, conduct internal reviews to support Distribution performance and other request from Line Manager.
Job Roles & Responsibilities:
- Manage the identification of sales area with heightened sales quality risk exposure via data analysis of persistency, CFI, lapse, surrender MI reports across agency sales regions on monthly basis
- Manage the review activities on monthly basis including insurance document retrieval, perform detailed review of insurance policies, customer profile and customer information change request, customer payment request; detailed review of agent profile with sales and service record such as insurance premium collection record, complaint record, result of independent controls performed by relevant stakeholders such as Mystery Shopping (MS), Welcome Call/Sales Quality Call Back (WCC/SQCB), underwriting result, claim result to identify suspicious indicators, sales malpractices and potential fraud activities
- Manage the validation activities to confirm the factual accuracy of suspicious indicators and fact findings via customer call back, sales management interview and/or field check together with Investigation team where required
- Collaborate with relevant departments including but not limited to Policy Services, NBUW, DA, Claim, Market Conduct, Contact Center, DA&I during the review/analysis activities to connect all dots for identification of sales malpractice trend, abnormal sales behavior trend
- Manage escalation and reporting to AD Management on monthly basis with suspicious indicators, fact findings, detailed case study, process control gaps, common pitfalls on periodic basis for remediation actions with relevant stakeholders
- Gain and update job knowledge to remain informed about novelty in the field.
- Other direct request from Line Manager.
Qualifications & Experience:
- BS degree in Finance and Banking, Economics, Statistic or related fields
- At least 5 years of experiences in risk and control, analysis, investigation, market conduct, compliance, audit or relevant field
- Experiences in banking, auditing, consulting in finance or insurance industry is an advantage
Knowledge and skills:
- Proven knowledge of sale performance, sale best practices/malpractices, operational controls, information security
- Proven working experience related to Analysis, Internal Control and/or Auditing, Risk
- Proficient in spreadsheets, databases, MS Office
- Sound and practical business acumen and business judgment
- Good analytical skill, negotiation skill, problem solving skill
- Professional communication skills, presentation, reporting in English and Vietnamese
- Hands on experience with reporting and analysis for the assigned indicators
- Has abilities to work independently with high quality of deliverables, to transfer knowledge and to deliver training
Prudential is an equal opportunity employer. We provide equality of opportunity of benefits for all who apply and who perform work for our organisation irrespective of sex, race, age, ethnic origin, educational, social and cultural background, marital status, pregnancy and maternity, religion or belief, disability or part-time / fixed-term work, or any other status protected by applicable law. We encourage the same standards from our recruitment and third-party suppliers taking into account the context of grade, job and location. We also allow for reasonable adjustments to support people with individual physical or mental health requirements.
Senior Quality Assurance Engineer - Aerospace Systems
Posted today
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Job Description
Key Responsibilities:
- Develop and implement robust quality assurance plans and procedures for aerospace systems.
- Conduct regular audits of manufacturing processes, product quality, and compliance with standards.
- Perform inspections and testing of components and systems to ensure adherence to specifications.
- Analyze quality data, identify trends, and lead efforts to address non-conformances.
- Implement corrective and preventive actions (CAPA) to resolve quality issues.
- Collaborate with engineering and production teams to integrate quality control throughout the product lifecycle.
- Ensure compliance with relevant aerospace industry standards and regulatory requirements.
- Prepare quality reports and present findings to management and stakeholders.
- Champion a culture of continuous improvement and quality excellence within the organization.
- Bachelor's degree in Engineering (Aerospace, Mechanical, Electrical) or a related technical field.
- Minimum of 5 years of experience in Quality Assurance or Quality Control within the aerospace or aviation industry.
- In-depth knowledge of quality management systems such as AS9100 and ISO 9001.
- Proficiency in statistical analysis tools and techniques (e.g., SPC, DOE).
- Experience with root cause analysis methodologies (e.g., 5 Whys, Fishbone diagrams).
- Strong understanding of aerospace manufacturing processes and materials.
- Excellent analytical, problem-solving, and critical thinking skills.
- Effective communication, leadership, and interpersonal abilities.
- Ability to work collaboratively in a team environment and manage multiple priorities.
Engineer - Supplier Quality Management ( Work Base Hai Phong)
Posted today
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Job Description
Mô tả công việc:
(Mức lương: Thỏa thuận)
Job Purpose:
Take care of the supplier management for the production of the product lines, including but not limited to Electronic Pen, tablet to ensure the production with reliable high-quality.
Key Responsibilities:
Work with engineering to introduce new project and move forward to smooth mass production.
Ensure production quantity at supplier and timely delivery to customer.
eview and improve production yield rate, pursue the continuous improvement of production capability of contracted EMS/ODM/supplier to achieve best cost.
ey parts vendor regular on-site check and quality improvement follow up.
romote supplier quality management based on the quality status feedbacked from customer & market.
ead the issue resolution and root-cause analysis processes associated with supplier quality issues.
erform audits at the EMS/Suppliers to ensure compliance with company strategy.
omplete other tasks assigned from the line manager.
Chức vụ: Nhân Viên/Chuyên Viên
Hình thức làm việc: Toàn thời gian
Quyền lợi được hưởng:
As company policy; 13th salary; Performance Bonus
Travel to oversea; Premium Health Insurance; Annual Health Check
Maximum 17 annual leave days/year.
Yêu cầu bằng cấp (tối thiểu): Đại Học
Yêu cầu công việc:
Bachelor's Degree or equivalent required, and ma in Electronic or Mechanical is preferred.
amiliar with production, 3 years or more experience on engineering or quality management in electronic or mechanical industry.
luent English in oral and writing, which can be as the working language, Japanese as 2nd foreign language is preferred.
ood office skills at Microsoft office such as Excel, PowerPoint, etc.
esult oriented, ability to multi-task, negotiation and problem-solving skills with partners.
team player, good communication and coordination skills which can support build interactions among multiple functions.
igh motivation, sense of responsibility, self-discipline & willing to learn.
Yêu cầu giới tính: Nam/Nữ
Ngành nghề: Quản Lý Chất Lượng (QA/QC),Sản Xuất/Lắp Ráp/Chế Biến,Điện/Điện Tử/Điện Lạnh
Đại Học
Không yêu cầu