• Managing manpower to achieve the monthly planning.
• Managing subordinates to produce products
• Monitoring and control line performance in order to promote high efficiency and good quality.
• Other related jobs
• Supervise all inspection data and manpower in QA.
• Responsible for SPC&R/M to supervise and analyze all data in manufacture & QA
• Review and manage customer quality requirements and work with customers to resolve and quality issue.
• Pay attention to ISO, Safety and environment system.
• Coach and train the operator/leader/supervisor on quality principle, methodology and tools.
• Other related Jobs
1.Research and develop new products, improve quality of product to meet the needs of customers and markets.
- New Product and process design
- New product planning and market research
- Current Product design changes
- Evaluation of alternative materials for cost reduction/discontinuance
- Sales support for the introduction of products into the market
2.Production support for new products (transfer to production section)
3.Cooperate with production department (chemical production section) and production department (QC section) for trial production of new products.
4.Prepare research and development related reports.
5.Creating and control of product specifications, user's manuals and technical documentation
6.Report the work progress to the supervisor.
7.Coordinate the job with related department/section.
8.Daily management of equipment, facilities
9.Other jobs as assigned by supervisory
- Promotion and supporting of carbon neutral activities at each production site in ASEAN region
- Setting policy, target and create roadmap for the achievement of carbon neutrality in ASEAN
- Information gathering such as carbon neutrality related laws & regulations, subsidies etc.
- Promotion of studied activities at each production site
- Human resources development on carbon neutrality and CO2 reduction
- Making annual budget and monitoring plan vs actual
- Collaborate with regulatory and cross-functional colleagues on clinical document reviews
- Provides support in the preparation of regulatory submissions for investigation and commercial products in line with FDA requirements, regional requirements, and scientific and company policies and procedures
- Successfully handle routine labelling changes and drug listings
- Performs work-flows and procedures regarding document tracking, indexing and retrieving, and disseminating information to the Regulatory department
- Keep up to date with changes in regulatory legislation and guidelines
- Offer advice about company policies, practices and systems
- Support analysis/activities/communications from RA perspective on product complaints, adverse events, and field actions, etc.
• Understand Company's quality standards and the quality requirements of customers and then communicate those information with supply partners to minimize the defect.
• Share and instruct necessary actions with team and partners to satisfy quality and delivery requirements.
• Improve quality level of supplier partners by introducing appropriate inspection and Kaizen process.
• Resolve issues that come up (defect, delay, accidents) .
• Collaborate with other department for continuous quality improvement.
• Participate in ISO system and related documentation such as Standard/Instruction.
• Knowledge of green procurement standard concerned with chemical substances and RoHS (Restriction of Hazardous Substances in Electrical and Electronic Equipment).
1. Basic knowledge of DWG, QC Process Chart, Inspection std.
2. Knowledge and understanding of the production process (MFG Process) Stamping Press
3. Good knowledge and ability to solve problems or Problem Solving.
4. Have knowledge and understanding of the IATF 1649 system (SPC, Process Capability, MSA).
5. Have basic knowledge and can use measuring tools well such as Vernier, Micro Meter etc.
6. Able to liaise with customers, suppliers, including summarizing the quality report to customers.
* Assist the QA/QC Engineer in conducting Good Practice Trainings, In-process Inspections, identifying defective works, conducting in-house testing, in-house Quality Assessment
* Lead a team of QA/QC Technicians and QC Inspector.
* Maintain and control QA/QC practices with regular checks and inspections ensuring correct operation and implementation of procedures.
* Able to follow material specification as instructed by QA/QC Engineers
-Support any Quality Regulatory Compliance related special projects that assigned by
company policy as well as by the change of Thai FDA regulation and requirement.
-Prepare, register, and gather documents related to registration process to get both new and
renew import licenses e.g. Certificate of Free Sale/ Certificate of Goods/ Free Sale
Certificate, ISO/ any other applicable standard certificate, product catalog/ brochure,
Instruction for use/ Notice, and declaration letter (if needed).
-Incorporate with QA/RA manager to oversee the changes and/ or new legislations,
requirements, applicable standard and/ or requirement that lead to impact to registration
process and Quality Management System.
-Gather, file, and maintain all data/ information regarding FSCA/ AE/ Customer Complaint
and any other related QA/RA issues.
-Act as Document Control Center to handling all quality and regulatory documents related to
applicable standard for Quality Management System.
-Support any Quality Regulatory Compliance related special projects that assigned by
company policy as well as by the change of Thai FDA regulation and requirement.
-Prepare, register, and gather documents related to registration process to get both new and
renew import licenses e.g. Certificate of Free Sale/ Certificate of Goods/ Free Sale
Certificate, ISO/ any other applicable standard certificate, product catalog/ brochure,
Instruction for use/ Notice, and declaration letter (if needed).
-Incorporate with QA/RA manager to oversee the changes and/ or new legislations,
requirements, applicable standard and/ or requirement that lead to impact to registration
process and Quality Management System.
-Gather, file, and maintain all data/ information regarding FSCA/ AE/ Customer Complaint
and any other related QA/RA issues.
-Act as Document Control Center to handling all quality and regulatory documents related to
applicable standard for Quality Management System.
- Manage and lead all facility, production, and administrative departments
- Ensure that the facility runs efficiently with the highest productivity possible
- Ensure that each department is producing products of the highest possible quality
- Conduct periodic inspections of all departments to ensure standards are met
- Maintain constant communication with employees, suppliers, and vendors
- Keep up to date on all current events and issues in the manufacturing industry
- Oversee safety protocols and programs
- Ensure that all employees and subcontractors are following all safety protocols
1. Plan and control production process.
2. Plan and control employees to produce according to standards.
3. Plan and support the preparation of work manuals according to IATF16949.
4. Invent ways to reduce working time to increase production efficiency.
5. Control expenses Departmental costs
6. Control and supervise reporting on production, quality, and waste.
7. Take care and maintain the environmental management standard system according to the regulations.