8 Manager Quality jobs in Thailand

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.

**We Put the World on Vacation**
Travel + Leisure Co. is the world's leading vacation ownership and travel membership company, with a dynamic and growing portfolio of resort, travel club, and lifestyle travel brands. Our dedicated associates help the company achieve its mission to put the world on vacation. Innovation and growth keep our work interesting and fun. Every day is a chance to learn something new and turn vacation inspiration into exceptional experiences for millions of travelers worldwide.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
· Complete and review all sales and finance documents with all new and upgrading owners,
· Provide pre and post-sale Count on Me! Service to ensure retention of the business and ensure compliance with all regulatory, Finance and business processes, policies and procedures,
· Ensure timely collection and processing of any information required by the company and or Finance By Wyndham, in order for the company to approve the Application for Vacation Credits, and for Finance by Wyndham to complete the loan assessment process supporting the purchase of Vacation Credits,
· Observe and identify any compliance concerns, patterns or any other issues detrimental to maintaining business retention and communicate such with the Site Project Directors and or Quality Assurance Manager ( where applicable), and conduct appropriate training with staff, or work with the site dedicated traniner.
· Active participant in sales and site management meetings,
· Any other duties as assigned by the Director Business Retention and Discovery and or, Quality Assurance Manager (where applicable),
**Where Memories Start with You**
Hospitality is at the heart of all we do at Travel + Leisure Co. Here, you'll find an inclusive environment where we deliver excellence and take time to have fun, celebrate together, and support one another. We're always looking ahead to what's next and how we can strengthen our business, its neighboring communities, and the customer experience. Join our global team and build a career where memories start with you.
We are an equal opportunity employer, and all applications will be considered for employment without attention to their membership in any protected class. If you require any reasonable accommodation to complete your application or any part of the recruiting process, please email your request to , including the title and location of the position for which you are applying.

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
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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
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+ © 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.

**What are my responsibilities?**
- Overseeing Quality Management systems at SMO Customer Service Project in Thailand to drive consistency and alignment and ensure ISO9001, and applicable customer requirement compliance and sustainable operations.
- Perform Quality Lead internal auditor and support implementation of follow-up corrective actions to ensure compliance with ISO9001/Customer/Head Quarter and applicable local regulations
- Driven and influencing organizations, management, and teams to maintain and develop Quality performance.
- Partnering with maintenance site to increase quality and safety awareness, tracking and monitoring Quality key performance indicators and driving continuous improvement efforts incorporation with Section Manager.
- Developing aligned methods, business processes and procedure for consistent of Quality Management System within SMO Customer Service, Thailand.
- Take role of Quality Manager in Project for maintenance project bidding/offering and ensure it’s fulfill with customer and Siemens requirement.
Lead implementation, best practice and lesson learned sharing including consultation in Quality perspective.
- Update quality documentation and communicate to carry forward lessons learned from quality concerns
- Resolve complex compliance matters, incident investigation relating to quality including use of required data and management systems
- To review and pre-approval on cost relating to quality on yearly basis.

**What do I need to qualify for this role?**
- Professional experience: Above 5 years working experience in Sciences/Engineering and related field of Quality Management System, or other Management System e.g Environmental, Occupational health and Safety in public transportation or similar fields.
- A detailed understanding of ISO9001/ISO14001/ISO45001 and experience in auditing.
- Project experience: Office administration, project or processes/event planning and organization
- Leadership experience: Coaching, decision making, analytical, problem solving
- Intercultural experience: able to communicate, interact, motivate, manage a variety of cross-functional team members and dealing with customers and suppliers
- Good in written, verbal and presentation skills
- Good in organizational and follow-up skills
- Be able to communicate and understanding in English writing, speaking, and listening.

**Organization**: Siemens Mobility
**Company**: Siemens Mobility Limited
**Experience Level**: Experienced Professional

**Job Type**: Full-time

**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

Our client is a global player in upstream pharma production globally, with over 20 manufacturing sites across the world. With their site in Thailand, they are looking for a Quality Systems Manager on-site to oversee site QS management and participate in improvement projects to enhance site quality & capability.

**Responsibilities**:
Reports to Site Quality Director; leading a small team of 3.

Overall management & supervision on quality system to ensure documentation processes are correctly followed and performed in a timely manner

Responsible for all quality systems related issues, including APR, Complaints, Change Control, Recall/Return, Audits, Documentation, Qualification/Validations etc.

Regular improvements and maintenance on all quality processes according to cGMP, ISO 9001 and other related requirements

Maintain and review Quality KPI metrics to monitor site performance & efficiency

**Requirements**:
Degree holder in any science or engineering related disciplines

Minimum 5 years of experience in QA/QC, preferably with extensive exposure in QS management under cGMP and ISO 9001.

Prior working experience within Pharma, Medical Devices or Chemical industries

A team player, attentive to details, excellent time management & organization skills.

Excellent in written and spoken English

Our client is a global player in upstream pharma production globally, with over 20 manufacturing sites across the world. With their site in Thailand, they are looking for a Quality Systems Manager on-site to oversee site QS management and participate in improvement projects to enhance site quality & capability.

**Responsibilities**:
Reports to Site Quality Director; leading a small team of 3.

Overall management & supervision on quality system to ensure documentation processes are correctly followed and performed in a timely manner

Responsible for all quality systems related issues, including APR, Complaints, Change Control, Recall/Return, Audits, Documentation, Qualification/Validations etc.

Regular improvements and maintenance on all quality processes according to cGMP, ISO 9001 and other related requirements

Maintain and review Quality KPI metrics to monitor site performance & efficiency

**Requirements**:
Degree holder in any science or engineering related disciplines

Minimum 5 years of experience in QA/QC, preferably with extensive exposure in QS management under cGMP and ISO 9001.

Prior working experience within Pharma, Medical Devices or Chemical industries

A team player, attentive to details, excellent time management & organization skills.

Excellent in written and spoken English