9 Regulatory Standards jobs in Thailand

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.

Our client is a global soft drinks company, one of the world's largest food and beverage companies.
- Conducting a regulatory check for compliance (in partnership with the local regulatory manager) and providing regulatory approval for Import and Export products.
- Being the point of contact for regulatory affairs of exporting countries to acquire the required regulatory package (product composition, seasoning specification and label) and registration documents.
- Reviewing product package for compliance with importing country’s regulatory requirements.
- Identifying information gaps and working with cross-functional teams to obtain the necessary information to achieve compliance with regulatory requirements and final regulatory approval.
- Providing regulatory support for product registration for importing countries.
- Reviewing and preparing the registration package for MU or local RA to proceed with registration.
- Providing all necessary support for any regulatory deficiencies may have.
- Developing the product label specification (PLS) for imported products.
- Developing product label specifications in accordance with local regulatory labelling requirements.
- Reviewing product labels and providing regulatory approval.

**Education and Experience**:

- 2-3 years experience in Regulatory Affairs from Food Business.
- Education in Food Science and other related field.
- Able to speak English would be preferred.

Regulatory.
TFDA.
Food.

**Responsibilities**:
Ensure product management comply with local regulation and company compliance policy.
Support all necessary regulatory information to related function.
Responsible for product registration, amendment, label and advertisement.
Maintaining and secure the regulatory database.
Build/enhance good relationship with TFDA and other government authorities and internal stake holder.
Manage the product registration of new countries and new phases of Cambodia and Myanmar.
Support Store on Product registration, Store Licenses, Store projects on Food Safety and all RA projects.

**Qualifications**:
Bachelor degree in Science, Pharmacy or related field.
Minimum 5 years working experience in regulatory affairs area especially in food.
Strong interpersonal, negotiation, communication and presentation skills.
Good command of written & spoken English including computer literacy.
High ability to learn with good attitude.
Ability to effectively manage projects and good human relation.

**Job skills required**: English, Negotiation, Compliance

Job Description Summary

To ensure all BD products with new MDR and IVDR labeling comply with all relevant local pre/post-market requirements for the country. Registration submission to support product registration in Thailand and OTA countries.

**Job Description**:

- Responsible for all activities associated with regulatory clearance for all products in the country which includes:

- Work closely with the Business Leads from the various BU to determine which products need to be included for registration
- Work with BD division RA (BURA) to obtain necessary information / documents (e.g. CFG / CFS, etc.)
- Compile documentation and ensure completeness and quality of registration dossier
- Submit registration dossier and follow through until regulatory clearance is obtained (if applicable)
- Review and Prepare change notifications or amendments of registered products for submission
- Submit change notifications or amendments of registered products (if required)
- Maintain and update list of registered products in the applicable platforms (e.g. SharePoint, RA Shared folders, RIM etc.)
- Support any post-market field action reporting to local MOH (if applicable)
- Where applicable, act as the main focal point for distributors pertaining to regulatory activities.
- Updates and maintain In-Country Registration Submission Tracker and Planner and other local requirements as deemed appropriate.
- Responsible to review and provide impact assessments for any changes to products. (e.g. change in packaging and labeling)
- Responsible for providing regulatory input and review for new product development projects, promotional materials, local country specific labeling if needed
- Undertake additional projects and tasks as assigned by the supervising manager
- Provide regulatory inputs for and participate in GDP audits where appropriate
- Build a good relationship with in-country junior regulators at the least (where appropriate)

**Requirements**:

- Degree in Pharmaceutical/Science/Biomedical or equivalent
- Minimum 2 years of working experience in a function related to regulatory or quality, preferably in the healthcare industry.
- Knowledge of quality systems or regulatory requirements preferably related to medical devices.
- Good team player
- Have good problem-solving acumen
- Independent, meticulous and communicates well
- Proficient in Microsoft Office (Word, PowerPoint, Excel)

Primary Work Location

THA Bangkok - The Offices at Central World

Additional Locations

Work Shift

Job Description Summary

To ensure all BD products with new MDR and IVDR labeling comply with all relevant local pre/post-market requirements for the country. Registration submission to support product registration in Thailand and OTA countries.

**Job Description**:

- Responsible for all activities associated with regulatory clearance for all products in the country which includes:

- Work closely with the Business Leads from the various BU to determine which products need to be included for registration
- Work with BD division RA (BURA) to obtain necessary information / documents (e.g. CFG / CFS, etc.)
- Compile documentation and ensure completeness and quality of registration dossier
- Submit registration dossier and follow through until regulatory clearance is obtained (if applicable)
- Review and Prepare change notifications or amendments of registered products for submission
- Submit change notifications or amendments of registered products (if required)
- Maintain and update list of registered products in the applicable platforms (e.g. SharePoint, RA Shared folders, RIM etc.)
- Support any post-market field action reporting to local MOH (if applicable)
- Where applicable, act as the main focal point for distributors pertaining to regulatory activities.
- Updates and maintain In-Country Registration Submission Tracker and Planner and other local requirements as deemed appropriate.
- Responsible to review and provide impact assessments for any changes to products. (e.g. change in packaging and labeling)
- Responsible for providing regulatory input and review for new product development projects, promotional materials, local country specific labeling if needed
- Undertake additional projects and tasks as assigned by the supervising manager
- Provide regulatory inputs for and participate in GDP audits where appropriate
- Build a good relationship with in-country junior regulators at the least (where appropriate)

**Requirements**:

- Degree in Pharmaceutical/Science/Biomedical or equivalent
- Minimum 2 years of working experience in a function related to regulatory or quality, preferably in the healthcare industry.
- Knowledge of quality systems or regulatory requirements preferably related to medical devices.
- Good team player
- Have good problem-solving acumen
- Independent, meticulous and communicates well
- Proficient in Microsoft Office (Word, PowerPoint, Excel)

Primary Work Location

THA Bangkok - The Offices at Central World

Additional Locations

Work Shift

More than just a recruitment company. At PRTR, we have been a part of our customer's success for 30 years as their total HR solutions partner. With 550 dedicated professionals and over 15,000 outsourced staff, we will continue to carry out our mission to develop a better career, a better life, and a better society, and thrive to become the No.1 people solutions organization in Southeast Asia.

**Roles & Responsibilities**
- Ensuring compliance with all regulatory requirements.
- Maintaining regulatory documentation database and determining and/or validating existing.
- Handling supplier's approval and development-Audit and Training all trollers.
- Ensuring the export items comply with food laws in the Philippines, Indonesia, Malaysia, Vietnam, China, Japan, the US, and Europe.
- Ensuring compliance with the requirements of third-party certifying bodies. Certifying audits (BRC. GMP, HACCP, Kosher, Halal, etc.) and all customer requirements.
- Ensuring Customer complaint handling program.

**Qualifications**
- Bachelor's or master’s degree in food science / Science.
- At least 5 years of experience in RA within the Flavour/food ingredients industry.
- Strong knowledge of Asia, US, and European Food legislation, and food safety standards.
- Familiar with the Thai FDA.
- Understand HACCP and quality management systems.
- Good personality, Flexible, Self-motivated, Leadership.
- Good command of English.

ยา/เภสัชกรรม

วันนี้
- คุณสมบัติพื้นฐาน
- งานประจำ- 3 - 5 ปี- สมุทรปราการ- ปริญญาตรีหรือสูงกว่า- ขึ้นอยู่กับคุณสมบัติและประสบการณ์- หน้าที่และความรับผิดชอบ

**Are you highly responsible persons?**

**Are you at your very best when there’s problem to be solved?**

**Are you an extremely excitable person?**
- Mega Lifesciences is looking for a R
- **egulatory Affair Pharmacist** to work closely with
- **Regulatory Affair Manager** in a fast-paced environment that will offer ample opportunities to learn and expand your experience and expertise.**Job Summary**
- As a
- **Regulatory Affair Pharmacist**, your key tasks are as below:
- Preparing CTD and ACTD dossiers for ROW markets
- Responsible for handling queries received from respective health authorities
- Preparing documents for filing relevant variations
- Coordinating with other departments and outsourced manufacturers for arranging documents related to product approvals.

คุณสมบัติ
- Applications are invited from the potential talents who meet the following criteria:
- Bachelor’s Degree or Master’s Degree in Pharmacy
- Minimum 3 - 5 years of experience in pharmaceutical industry or in Drug Regulatory affairs
- Experience in a global/matrix environment or cross-functional teams in the
- Pharmaceutical industry or in clinical research
- Fluency in English - written and verbal
- Self-motivated individual with organizational skill
- Creative, hardworking, and strong problem solving ability
- Ability to work under pressure and meet deadlines.
- Open & Interested to work in Bangpoo, Samutprakarn

**Skill & Knowledge**Benefits**:

- Salary increment
- Annual leave
- Yearly bonus
- Provident fund
- Life insurance
- Medical insurance (IPD & OPD)
- Telemedicine
- Health checkup
- Uniform
- New Year party
- Good Health by Yourself activities
- etc.
- If you are eager to make the most of this opportunity, then press APPLY in this job posting OR please send your resume via
- For further information, please call
- ** 02-709-3600 ext. 4857 (K.Nitchapon).**

ดูคุณสมบัติเพิ่มเติม
- สวัสดิการ
- Good Health by Yourself activities
- Health checkup
- Life insurance
- Medical insurance (IPD & OPD)
- New Year party
- Provident fund
- Salary increment
- Uniform (provided but not compulsory)
- ทำงานสัปดาห์ละ 5 วัน
- ประกันสังคม
- โบนัสประจำปี

ดูสวัสดิการเพิ่มเติม