12 Quality Manager jobs in Thailand

Company Description
**Location**:Robert Bosch Automotive Technologies (Thailand) Co., Ltd., Hemaraj Industrial Estate, Tasith, Pluak Daeng, Rayong, Thailand

Do you want beneficial technologies being shaped by your ideas? Whether in the area of mobility solutions, consumer goods, industrial technology of energy and building technology - with us, you will have the chance to improve quality of life all across the globe. Welcome to Bosch.

This site is the **integral manufacturing plant and R&D Center**. It is the first smart factory in Thailand. It will enable us to respond to growing automobile production in Thailand and to serve international as well as local automotive customers on the spot. The supplier of technology and services is focusing heavily on connected manufacturing at the factory.

**Manufacturing Plant**:The Company is constructing its first plant of the manufacturing of gasoline injection systems in Thailand. It is capable of production 1 million fuel injector units every year. With the new fuel injector plant we are able to meet the increasing demand of our customers in the region.

**R&D Center**: The R&D office and laboratory are located on same site as production. In order to have dedicated laboratory accommodating automotive specific machine and equipment such as fuel testing benches and Noise, Vibration, Harshness chambers.

**Job Description**:
**Key Responsibilities**: Leader of connector team in PS/QMM1-HmjP to prepare and support customer requirements such as PPAP, customer complain, etc.
- Leader of the Connector team in PS/QMM1-HmjP (CC-associates development, Task monitoring, LPC)
- Prepare and submit PPAP (Production Part Approval Process) to customer
- Customer complaint handling
- Prepare and execute customer audit
- 14Q, FMEA walk, quality activities and find opportunities to improve quality together with other department
- SAP Key User
- Fulfill other assigned jobs by Quality Group Leader

**Qualifications**:
**Educational Background**:

- B.A. Degree of Engineering or related field

**Qualifications**:

- Good command of English
- Experience to lead the team of Quality Engineer in quality areas and shop floor area
- At least 5 years work experience in quality control or quality assurance (manufactory environment)
- or manufacturing engineer
- QMS knowledge (IATF, CDQ)
- IATF core tools knowledge
- Connector product knowledge
- SAP knowledge
- Microsoft office tools

Additional Information
**Your future job offers you**

Housing allowance, company shuttle, free lunch, provident fund, medical benefits, OPD, IPD, dental benefits, performance bonus, service year reward, insurance, diligent allowance, marriage allowance, new born gift, oversea allowance, etc.

**Make it happen**

Interested applicants are invited to submit your CV, current & expected salary, and contact information.

**Follow us on Facebook : Bosch Thailand Career

Manager - Quality
TE Connectivity is a global industrial technology leader creating a safer, sustainable, productive, and connected future. Our broad range of connectivity and sensor solutions enable the distribution of power, signal and data to advance next-generation transportation, renewable energy, automated factories, data centers, medical technology and more. With more than 85,000 employees, including 8,000 engineers, working alongside customers in approximately 140 countries, TE ensures that EVERY CONNECTION COUNTS. Learn more at and onLinkedIn, ( Facebook, WeChat, ( Instagram andX (formerlyTwitter). ( Our core values are **integrity, accountability, inclusion, innovation and teamwork** .
**Job Overview**
Develop and improve quality procedures and system; and monitor the quality control activities **with the objective** of achieving business development requirements **within** the QS and global policies, procedures and guidelines.
**Job Requirements**
**Planning and Budgeting**
Develop and implement department budget and plan, allocate department target to subordinates, monitor their performance and the achievement of the budget in order to achieve targeted department performance.
**Policies and Procedures**
Localize and oversee the implementation of global quality policy, procedures and systems; and review QA reports within the entire factory to ensure the business procedures in line with QS and global standards.
**People Management and Development**
Allocate and balance work across direct reports; review and provide timely performance feedback to direct reports; mentor, develop and motivate them; and help resolve people/functional issues in the team in order to achieve targeted department performance and retain key talent.
**Quality System**
Set up and monitor the implementation of the quality policies, including internal audit policy; oversee effectiveness of quality system; visit key accounts; provide feedback towards the quality-related best practices to global quality team; and coordinate audit from key customers and third parties to meet business development requirement and align with global quality policy.
**Quality Engineering**
Visit key suppliers and drive their quality performance improvement; resolve key customers complaints; review factory quality performance and set up process quality improvement plan and monitor the implementation in order to improve factory and suppliers' quality performance.
**Quality Control**
Supervise the implementation of quality control for income/in-process/final productions; and initiate internal quality audit; provide professional advice and coordinate key quality issues with related departments in order to ensure product quality to meet customer/regulatory requirements
**Testing**
Review current testing capability situation; and develop testing capability improvement plan to meet business development requirements
**What your background should look like**
+ Bachelor degree with engineering and technology major background
+ 15 years quality working experience in MNC, including 5 years managerial experience
+ Excellent verbal and written communications skills in both Thai and English
+ Initiator / Ability to work with limited guidance
+ Strong Analytical Skills
+ Strong Project Management and Organization Skills
**Competencies**
SET : Strategy, Execution, Talent (for managers)
Location:
Lamphun, 51, TH, 51000
City: Lamphun
State: 51
Country/Region: TH
Travel: 10% to 25%
Requisition ID: 139106
Alternative Locations:
Function: Quality
TE Connectivity and its subsidiaries, affiliates, and operating units (collectively, the "Company") is committed to providing a work environment that prohibits discrimination on the basis of age, color, disability, ethnicity, marital status, national origin, race, religion, gender, gender identity, sexual orientation, protected veteran status, disability or any other characteristics protected by applicable law or regulation.

Join our global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes to our patients. We are all in it together to make a difference. Be a part of a culture that doesn't just wait for change but actively creates itwhere your skills and values drive our collective progress and impact.
**Job Description:**
+ Work as a regional RA leader to prepare registration strategy, submission plan and coordinate registration submissions in APAC, Thailand, Philippines, Malaysia, Singapore, as well as other south east Asia countries;
+ Lead country team and global team to prepare submission dossiers, interact and coordinate the interaction with different health authorities;
+ Work as a key contact point for APAC regulatory intelligence, proactively search and monitor policy and regulation changes from health authorities, work with cross functions to analyze the impact of regulatory environment changes to the companys products and business, and update to key stakeholders timely;
+ Overall monitor the registration projects in ASEAN countries, make sure product approvals on time, timely update and report to all stakeholders;
+ Review and approve advertising, promotional materials and labeling to ensure regulatory compliance;
+ Maintain QMS and certification within the sites, including the the control of quality procedures and records
+ Oversee quality processes such as product releases, product re-labelling, complaint investigations and reporting, change control, non-conformance, correct and preventive actions.
+ Monitor 3PLs, suppliers, service providers and distributors with regards to maintenance of product quality and compliance to quality procedures, through regular checks and audits
+ Create quality awareness and educate and train employees on the organization QMS, local regulations and certification requirements
+ Ensures each sites audit readiness and manage external regulatory and corporate inspections to ensure full compliance. Coordinate internal audits within the sites
+ Escalate critical quality issues and lead any field service corrections / market actions
+ Perform post-marketing materiovigilance activities such as reportability assessments for complaints, submission of medical device event reports as required by applicable local laws and regulations, respond to regulatory agencies inquiries on serious Injury and/or Device Malfunction.
**Qualifications:**
+ Bachelor degree or above in life science, engineering or mechanical discipline;
+ 8-10 years regulatory affairs experience in MNC, familiar with medical device registration in ASEAN countries, other APAC countries in a plus;
+ Good project management and interpersonal skills, team player with the ability to work independently in a fast-paced and dynamic environment;
+ Experience of active device registration, laser or RF device registration is a plus, aesthetic device is a plus;
+ Basic ISO9001, ISO 13485, GMP and GDP knowledge, auditing Skills (preferred)
+ Fluency in written and spoken English, other languages in ASEAN countries is a plus.
We are an Equal Opportunity Employer. EOE Disability/Veteran. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates collaboration.

Identify business process pain points based on management's direction by analyzing current operational data.
Initiate business processes, strategies, and process designs and align with the current process to enhance the overall process and enhance business competitiveness.
Redesign management infrastructure system and improve in accordance with the related process operation standards. accordance with the related process operation standards.
Develop process performance indicators and analyze operational levels by monitoring abnormal situations.
Lead and follow up to ensure the new business process is well implemented.
Required
Qualifications Bachelor's degree in business management, Industrial engineering or a related field of study.
At least 5+ years of experience in process improvement.
At least one year of experience supporting senior and executive-level client decision-making and proactively anticipating stakeholders need.
At least one year of experience developing new and re-designing existing processes to meet new and/or evolving business requirements.
At least one year of experience facilitating group meetings or workshops to achieve desired outcomes and achieve consensus, with stakeholders.
Preferred Process improvement and/or project management certification (e.g., Lean Six Sigma Green Belt, CAPM, PMP).
Experience using quality improvement programs (e.g., Total Quality Management, Six Sigma).
Project management experience.
Strong oral and written communication skills to various audiences in a professional business environment.
Experience analyzing large and complex data sets, including a demonstrated thorough aptitude for conducting quantitative and qualitative analyses.
Demonstrated ability to collaborate and contribute as a team member: understanding personal and team roles, contributing to a positive working environment by building solid relationships with team members, and proactively seeking guidance, clarification and feedback.
Demonstrated ability identifying and addressing client needs, building relationships with clients, developing requests for information, demonstrating flexibility in prioritizing and completing tasks, and communicating potential conflicts to a supervisor.
Experience prioritizing and handling multiple tasks, researching and analyzing pertinent client, industry and technical matters, and utilizing problem-solving skills to achieve desired outcomes Skills and Qualifications

**Job skills required**: Project Management, Industrial Engineering

Req ID: 125736
Remote Position: No
Region: Asia
Country: Thailand
State/Province: Chonburi
City: Laem Chabang
**Summary**
Oversee Supplier Quality and manages and sets direction for semi-skilled and entry-level professional personnel. Provide direction, coordination, education and tools needed to achieve and maintain the site Quality Management System and enable the achievement of quality objectives.
#LI-TP1 #LI-Onsite
**Detailed Description**
Performs tasks such as, but not limited to, the following:
+ Supports generation of performance metrics for products and processes of relatively low complexity, and drives the team to achieve Quality Goals set by management (i.e.: DPQL, Total Quality at Celestica ( )), following industry standards such as ISO, IPC, AS, TL
+ Leads Quality Improvement Programs (QIP) in support of customer requirements and expectations that are considered small in scale and low in complexity.
+ Mentors and trains personnel in the practices of Quality management and Quality improvement (succession development)
+ Resolves customer issues of low difficulty using quality tools: Root Cause Analysis and Corrective Actions that are effective and timely.
+ Provides leadership and support in a variety of areas such as, analysis of nonconforming materials and customer return material authorizations.(RMA's), coordinating ESD compliance, supporting customer and 3rd party audits, and the administration of Quality management (Documentation, Change Control, Corrective & Preventive Actions and Calibration)
+ Supports new customer qualification and New product introduction with supplier assessments, First Article Inspections and oversee generation of product documentation for products / programs that are relatively low risk
**Knowledge/Skills/Competencies**
+ In-depth knowledge of quality metrics, ISO standards and processes.
+ Knowledge of Lean and Six Sigma Manufacturing processes and controls including: Statistical Process Control (SPC), 5S and Value Stream Mapping (VSM)
+ Good knowledge of Quality Management tools including: **Failure Mode and Effect Analysis (FMEA)** and development of **Quality Control Plans**
+ Strong Project Management Skills
+ Ability to coordinate a wide variety of resources to meet production quality and quantity metrics.
+ Ability to effectively communicate with a wide variety of internal and external customers.
+ Ability to effectively lead, manage, train and motivate a diverse group of employees to achieve high production levels within tight time deadlines and in a ~highly dynamic manufacturing environment.
+ Ability to use some or all of the following PC applications: Google Applications, Word, Excel, and PowerPoint.
+ Strong knowledge of the manufacturing processes
+ Excellent communication in English
**Typical Experience**
+ 8 years total working experiences with at least 4-6 years in manager/supervisor roles.
+ Industry expereinces in Electronics Manufacturing or Automotive.
**Typical Education**
+ Bachelor's Degree in related field of study, Engineering is preferred.
**Notes**
This job description is not intended to be an exhaustive list of all duties and responsibilities of the position. Employees are held accountable for all duties of the job. Job duties and the % of time identified for any function are subject to change at any time.
Celestica is an equal opportunity employer. All qualified applicants will receive consideration for employment and will not be discriminated against on any protected status (including race, religion, national origin, gender, sexual orientation, age, marital status, veteran or disability status or other characteristics protected by law).
At Celestica we are committed to fostering an inclusive, accessible environment, where all employees and customers feel valued, respected and supported. Special arrangements can be made for candidates who need it throughout the hiring process. Please indicate your needs and we will work with you to meet them.
**COMPANY OVERVIEW:**
Celestica (NYSE, TSX: CLS) enables the world's best brands. Through our recognized customer-centric approach, we partner with leading companies in Aerospace and Defense, Communications, Enterprise, HealthTech, Industrial, Capital Equipment and Energy to deliver solutions for their most complex challenges. As a leader in design, manufacturing, hardware platform and supply chain solutions, Celestica brings global expertise and insight at every stage of product development - from drawing board to full-scale production and after-market services for products from advanced medical devices, to highly engineered aviation systems, to next-generation hardware platform solutions for the Cloud. Headquartered in Toronto, with talented teams spanning 40+ locations in 13 countries across the Americas, Europe and Asia, we imagine, develop and deliver a better future with our customers.
Celestica would like to thank all applicants, however, only qualified applicants will be contacted.
Celestica does not accept unsolicited resumes from recruitment agencies or fee based recruitment services.

**About UOB**:
United Overseas Bank Limited (UOB) is a leading bank in Asia with a global network of more than 500 branches and offices in 19 countries and territories in Asia Pacific, Europe and North America. In Asia, we operate through our head office in Singapore and banking subsidiaries in China, Indonesia, Malaysia and Thailand, as well as branches and offices.

Our history spans more than 80 years. Over this time, we have been guided by our values — Honorable, Enterprising, United and Committed. This means we always strive to do what is right, build for the future, work as one team and pursue long-term success. It is how we work, consistently, be it towards the company, our colleagues or our customers.

**About the Department**:
Group Technology and Operations (GTO) provides software and system development, information technology support services and banking operations.

We have centralized and standardized the technology components into Singapore, creating a global footprint which can be utilized for supporting our regional subsidiaries and the branches around the world. We operate and support 19 countries with this architecture to provide a secure and flexible banking infrastructure.

Our Operations divisions provide transactional customer services for our businesses while also focusing on cost efficiency through process improvements, automation and straight through processing.

**Responsibilities**:
**Job Requirements**:
**Be a part of UOB Family**:

**Our Global Company**
**Access countless opportunities to advance your career**
**Fresenius Medical Care offers products and services along the entire dialysis value chain from a single source. As of December 31, 2023, we cared for more than 332,000 patients in our global network of roughly 4,000 dialysis clinics. At the same time, we operated around 40 production sites on all continents, to provide dialysis products such as dialysis machines, dialyzers and related disposables.**
**Corporate Headquarters**
**Fresenius Medical Care's corporate headquarters is in Bad Homburg v. d. Höhe, Germany. The North American regional offices are located in Waltham, Massachusetts, the Asian-Pacific regional offices are located in Hong Kong and the South American regional offices are in Rio de Janeiro, Brazil.**
**Our corporate headquarters coordinates activities at an international scale in close collaboration with regional headquarters across the globe.**
The function assures that all water treatment systems (WTS) and concentrate delivery and production systems are set up to achieve the dialysis fluid quality in compliance with the corresponding FME standards as well as legal and other external requirements in the most efficient way, at regional level and collaborate with the local technical operations. This is mainly achieved by establishing and maintaining a proper operational monitoring, microbiological and chemical test system as well as supporting the required system validation, monitoring and training system.
**Tasks performed regularly which form the essential characteristics of the position.**
**Operations according to Care Delivery International APAC Water Quality Standard**
- Implementation of a monitoring, reporting and training system related to dialysis fluid quality and water treatment system parameters as input for data evaluation (e.g. quarterly reporting of relevant parameters by the clinic to country headquarter) including
- Training of qualified personnel for routine monitoring and water quality related activities
- Approval of accreditation of proper laboratory
- Supervise WTS and dialysis fluid quality monitoring process in dialysis clinics including:
- Periodic evaluation of routine monitoring results (e.g. data correctness, compliance with fluid quality requirements)
- Root-cause analysis and risk evaluation in the case of critical deviations in dialysis fluid or WTS parameters, with the assistance of regional & local Technical Operation and Nursing and Clinic Quality Management Team.
- Performance of risk assessments for e.g. concurrent validation, deviations from requirements, etc.
- Execution of immediate correction and corrective actions / risk reduction measures in case of critical deviations of dialysis fluid quality or water treatment parameters, with the assistance of regional & local Technical Operation and Clinic Quality Management Team.
- Immediate reporting to CDI management in case of critical deviations of dialysis fluid quality or WTS parameters
- Support of the responsible functions at clinic and country level in implementation of
- Work with local Technical Operations Team (TO), Project Planners (PP) and external vendor (if required) to the selection of water treatment and concentrate delivery systems, validation, routine monitoring, disinfection and sampling plans, etc. to ensure the proper operations of the WTS
- Immediate correction and corrective actions in the case of deviations of dialysis fluid quality or WTS parameters
- Gap analysis based on the retrospective annual validation and legal requirements including evaluation of resulting costs (i.e. project management for the directive implementation)
- Optimise dialysis fluids and water treatment related costs in cooperation with e.g. real estate and facility management function in compliance with FME's eco-control targets, with the assistance of the local TO/PP
- Planning of validation and re-validation processes, with the assistance of the local TO/PP
- Training of qualified personnel in the implementation of the validation/re-validation processes
- Cooperate with interface at local and at corporate headquarters, e.g. Technical Operations, Care Operations Establishment of network and close collaboration with technical experts, e.g. clinic technicians, WT project engineers, etc. and international FQR community
- Define targets and follow up on achievement
- Document all relevant reports, e.g. re-/ validation, risk assessments, disinfection and sampling protocols etc. in an organized and well-structured way
- Support local country organisation and management during internal and external audits by providing audit relevant documents and participation during audit
- Supervise and support the APAC Country FQR.
**Quality, Legal & Compliance**
- Follow and comply with all relevant FME policies, guidelines, manuals and SOPs in the version as amended from time to time ("FME Policies")
- Keep yourself updated about the current version of the FME Policies that are relevant for your role and integrate corporate values in daily business
- Legal requirements must be considered for defining the local responsibilities on authorization / release of dialysis fluids production equipment in the dialysis clinics (e.g. medical director, centre responsible, pharmacist)
**Key Performance Indicators**
- Provide information to respective Country Managing Director, Area Manager of business location in APAC, and participate in optimising total cost of ownership for water treatment systems.
- Reduction of WTS' contamination incidence rate
- Meeting legal & regulatory requirements and Local & FME compliance standards
**Qualifications, experience, know-how and skills critical for success***
**1) Required training and education:**
- Academic degree with additional specialized qualification or subject-related education, preferably in technical, engineering or healthcare services
- Project Management Experience on Water Treatment Systems
- Knowledge on international and regional regulations on Water Treatment Systems
- Preferably, Corporate FQR's qualification training on international/local legal regulations, corporate water directives, microbial management and basic WTS engineering
**2) Required professional experience (in years):**
At least 2-4 years professional experience in equivalent or similar functions ideally in a technical, engineering, healthcare or healthcare-related business environment
**3) Required personal competencies:**
- Highly professional attitude characterized by a result, quality, patient and customer-oriented working style
- High social competence paired with persuasiveness and self-confidence, high level of energy and positivity based on a sincere personality
- Team Player with a strong drive to create positive work environment, able to motivate, empower and connect teams
- Strong structured methodical approach leading to pragmatic and effective solutions
- Strong ability to set priorities and self-manage high volume workload
- High ability to think strategically and take qualitative decisions even under changing conditions or conflicting requirements
- High analytical and problem-solving skills with proven ability to organize and analyse data
- Very structured way of working with strong focus on efficient and effective processes even under pressure
- Hight level of change, negotiation and conflict management skills
- Basic skills in presentation, facilitation and training
- High resilience and flexibility
**4) Other specialized knowledge, expertise and skills:**
a) Technical knowledge
- Understanding of technical aspects of the water treatment system components and other related medical devices and products
- Awareness of the potential impacts of contaminated water/dialysis fluids on dialysis patients
- Chemical and microbiological knowledge related to water and dialysis fluids
- Knowledge of the applicable legal and IMS requirements
- Ability to evaluate the economic impact of decisions
b) IT skills
- Understand and use modern communication software and systems 
- Good IT user knowledge (MS Office, Intranet etc.) 
- Understand basics of e-health, data security and related topics
- Basic knowledge of EuClid desirable
c) Languages
- Country language and English fluent as a must (presenting, writing, reading)
- Other languages besides country language an asset
5) Special personal requirements:
Please list requirements such as willingness to travel or work weekends or shifts etc.
- Working for an international company with international standards 
- Travelling within the region and international across different time zones

Quality Assurance Supervisor
Job ID
226055
Posted
27-Jun-2025
Service line
Advisory Segment
Role type
Full-time
Areas of Interest
Building Management, Facilities Management, Property Management
Location(s)
Bangkok - Krung Thep Maha Nakhon - Thailand
**KEY FUNCTIONS:**
Be responsible for developing and implementing quality assurance processes to maintain service quality, process efficiency, and operational compliance with internal standards and external regulations. This role involves leading a team, conducting inspections and audits, and driving continuous improvement initiatives.
**RESPONSIBILITIES:**
**Site inspection and Internal Audit**
+ Supervise managed building team to ensure full compliance with ISO Operational, Engineering, Accounting and HSE requirements.
+ Perform regular inspections of managed buildings to ensure practical alignment of building operations and company standards and requirements.
+ Identify problems and follow up with operation team to the timely investigation and resolution of complains.
+ Plan and execute Quality Assurance practices in corporation with ISO and internal audit activities.
+ Supervise and cooperate with internal team across functional team to address and solve quality/service issues or drive improvement to meet customer satisfaction.
+ Prepare a QA report to Property Management Team in monthly basis.
**ISO Standard Audit**
+ Oversee the effective implementation, maintenance and improvement the internal process to comply with the ISO standard and related requirement such as ISO Audit, KPI report and Management Review.
+ Manage ISO documentation, including Management Manuals, System Procedures (SP), Standard Operation Procedure (SOP), Work Instruction (WI), and Forms.
+ Update PFMR documents, Action plan and P-FMEA with division concerned to ensure that all control documents will be available for audit process and managed buildings.
+ Ensure that document records and reports provided to QMR (PFMR) with accuracy.
+ Review effectiveness of PFMR documents, Corrective Action Request (CARs) and Preventive Action Request (PARs) before closure.
+ Contributing and supporting to DCs team on document control approval and document announcement.
+ Act as a main representative to coordinate and support internal and external audit mandatories (Consultant & Certified Body) as part of ISO certificate surveillance and renewal.
**QUALIFICATIONS:**
+ Bachelor's degree in quality management, Business Administration, or related field.
+ At least 5 years working experience in the role of Quality Assurance / Quality Control / or Quality Management.
+ Strong ISO knowledge and holding ISO Certification or training in ISO standards (ISO internal audit is a must).
+ Involvement in implementing ISO 9001, ISO 14001, ISO 45001 or ISO 41001 standards is preferrable.
+ Strong attention to detail and analytical skills.
+ Ability to multitask, prioritize, and manage time efficiently.
+ Effective communication in English (verbal and written).
+ Proficiency in MS Office such as Words, PowerPoint, Excel, and QMS system.
CBRE, Inc. is an Equal Opportunity and Affirmative Action Employer (Women/Minorities/Persons with Disabilities/US Veterans)

Supplier Quality Assurance Specialist
Company : Safran Cabin
Job field : Purchasing
Location : Lamphun , Thailand
Contract type : Permanent
Contract duration : Full-time
Required degree : Bachelor's Degree
Required experience : More than 8 years
Professional status : Professional, Engineer & Manager
Spoken language(s) :
English Fluent
Thai Mother tongue
# 2025-160007
Apply with one click Any questions ?
**Job Description**
3.0 Detailed department related duties
Summary of Duties
3.1 Responsible for ensuring quality compliance of parts /materials to meet product /part specification and standard related.
3.2 Control and monitor parts quality and on time delivery of suppliers
- Responsible for the incoming inspection team to ensure they perform according to WI of inspection works and that all incoming inspection detail is correct.
- Use statistical approach to monitor quality data of the supplier and publish weekly/month report basis or any report request.
- Collect and evaluate supplier quality and on time delivery data to identify process improvement opportunities within the supply chain.
- Maintain supplier quality and on time delivery metrics and provide regular feedback to all suppliers
3.3 Lead effort to resolve supplier quality issues.
3.4 Review and analyze supplier non-conformance reports, perform internal investigation and participate in material review board.
3.5 Work directly with supplier to investigate rot cause and identify/follow up corrective actions.
3.6 Issue NCR and or 8D to suppliers and coordinate with purchase team to follow their corrective action.
- Verify the defect of material issue related
- Initiate and follow-up Supplier Corrective Actions (SCAR) in partnership with Manufacturing Engineering to ensure complete and effective root cause analysis and corrective action implementation.
- Manage suppliers' non-conformances, including their disposition, documentation, and communication.
- Validate the action items by quality control technics, communicating with suppliers.
3.7 Perform supplier audits to evaluate supplier compliance to SAFRAN requirements and audits required for supplier approval/re-approval process. Follow up on corrective actions resulting from audit findings.
3.8 Implement quality-related action plans to enable suppliers to achieve an acceptable performance level.
3.9 Provide assistance to suppliers on new products, process capability improvements, quality systems development.
3.10 Work with Engineering Team and Sourcing team to evaluate potential suppliers.
- Evaluate potential suppliers' quality management systems.
- Ensure that the right quality, customer flow down and regulatory requirements are properly called out on the drawings, purchase orders, and contracts before their transmission to suppliers.
- Conduct capability assessments that verify supplier qualifications, and travel to assigned suppliers.
3.11 Participate as a member of the Material Review Board to review and disposition Supplier related Nonconformance Material Reports as required
3.12 Assist supplier on product qualification and first article inspection activities
3.13 Lead Advanced Product Quality Planning (APQP) activity as assigned from manager.
3.14 Assure that all supplier quality related activities are conducted in compliance with the SAFRAN Standard.
3.15 Supervise and coach SQA Engineer.
**Job Requirements**
4.1 Thai Nationality only.
4.2 Complete bachelor's degree in ME/IE/EE or any field related.
4.3 Experience: 5 years of progressive quality experience in aerospace, automotive or mechanical manufacturing environment with the ability to lead and influence others. AS/ISO standards. Experience in supplier quality audit is preferable.
4.4 Ability to read and understand drawing, technical specifications, technical report, etc.,
4.5 Ability to write technical documents, audit reports, non-conformance dispositions
4.6 Strong knowledge APQP, PPAP, 8D and FAI Process
4.7 Capable of MS. Office and other Application.
4.8 Other Skills: Must be very organized, detailed oriented, systematic and accurate. Strong problem-solving skills. Knowledge of Lean and six sigma tools is desired.
4.9 Fluent communication in English is mandatory. Additional languages are a plus.
**But what else? (advantages, specific features, etc.)**
3.16 Cooperate with teams related on problem solving, quality improvement activities.
3.17 Implement SAFRAN specification and standard on concern process.
3.18 Process improvement as project assign.
3.19 Lead and coach supplier quality engineer.
3.20 Support and represent Supplier Performance Management Manager as assign.
3.21 Reduce Quarantine Inventory of RTV.
3.22 FAI Report review and approval.
3.23 Weekly/Monthly/Quarterly reports.
**Company Information**
Safran is an international high-technology group, operating in the aviation (propulsion, equipment and interiors), defense and space markets. Its core purpose is to contribute to a safer, more sustainable world, where air transport is more environmentally friendly, comfortable and accessible. Safran has a global presence, with 100,000 employees and sales of 27.3 billion euros in 2024, and holds, alone or in partnership, world or regional leadership positions in its core markets.
Safran is in the 2nd place in the aerospace and defense industry in TIME magazine's "World's best companies 2024" ranking.
Safran Cabin designs, certifies, manufactures and supports innovative aircraft cabin interiors, equipment and systems, providing airlines and OEM Customers with distinctive aircraft branding, and their passengers with a safe, comfortable and enjoyable flying experience.
**Locate your future workplace**
Ban Klang, Mueang Lamphun District51000
Lamphun
Thailand
100,000
employees worldwide
27
Number of countries where Safran is located
35
business area families
+ Maps are available under theOpen Database Licence ( .
+ © OpenStreetMap ( contributors.
+ © Safran
Safran is an Equal Opportunity Employer
All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, or other legally protected status.