Total 1,035 quality control manager job vacancies in Quality Assurance / Control category in The Philippines

Key descriptions
1) incoming & Outgoing goods /weight verification & control
2)Quality Inspection
3)DOCUMENTATION & RECORD KEEPING
4)PROCESS MONITORING
5) REPORTING & RISK CONTROL
6)CUSTOMER & VISITOR HANDLING
7)Coordination & crosschecking
8)Discrepancy reporting
9)EQUIPMENT MAINTENANCE

REQUIREMENT
EXPERIENCE IN RECYCLING ,metal trading,warehouse ,or logistic enviromennt isan advantage
Strong attention to detail andintegrity
Basic computer skills for recordkeeping
Physically fit and able to work inwarehouse environment
Responsible and able to workindependently

• Conduct in-process and finished product checking and standardisation.
• Monitor product quality and assist in trouble shooting.
• Manage and supervise laoboratory staffs during shift duty.

Requirements:

• Degree in Food Technology or Food Science or
• Diploma in Chemical Process (food option) with 3 years of experience
• Willing to work on Sundays and Public holidays (occasionally)

MAIN DUTIES AND RESPONSIBILITIES:

* Inspection of in-coming parts for release to manufacturing.

* Identify and analyse non-conforming parts for corrective action.

* Record, document and maintain inspection records.

* Assist in vendor audit and development.

MAIN JOB SPECIFICATIONS / REQUIREMENTS:

* Nitec/NTC/ITC in Mechanical Engineering or its equivalent.

* Minimum 2 years' relevant experience in fabrication environment.

* Ability to use Venier Caliper, Micrometer, Height & Depth Gauge, Profile Projector, Gauge Block and Smart Scope.

* Ability to read and interpret technical drawings.

Key Responsibilities 

• Produce monthly QA/QC status reports.
• Manage companywide nonconformities and claims. 
• Collaborate with cross-functional teams (QA, QC, Engineering, Production) to gather and validate documentation inputs. 
• Ensure all documents comply with internal policies and external regulatory standards (e.g., ISO 9001, ISO 14001). 
• Support internal and external audits by preparing and organizing required documentation. 
• Assist in development, review, and maintain quality documentation including SOPs, work instructions, inspection protocols, and quality manuals. 
• Assist in maintenance document control systems, ensuring version control and proper archival of obsolete documents. 
• Analyse performance data to identify areas for improvement. Measure the impact of improvements and adjust strategies. 

Qualifications & Requirements:

• Bachelor’s degree or Diploma in Mechanical Engineering, Industrial Engineering, or a related field.
• Minimum 2–3 years of relevant experience in a quality assurance within a manufacturing environment
• Proven experience in quality auditing, quality assurance, or similar roles within a manufacturing or engineering environment.
• Strong understanding of quality management systems (QMS), including ISO 9001.
• Exceptional communication and interpersonal skills, with the ability to work collaboratively across departments and present findings to various levels of management.
• Strong analytical and problem-solving skills; ability to interpret engineering drawings and technical specifications.
• Ability to work independently, prioritize tasks, and collaboratively in a fast-paced, dynamic environment, with a strong focus on customer satisfaction and continuous improvement.
• Detail-oriented, with the ability to handle multiple priorities and meet deadlines in a fast-paced environment.
• Strong problem-solving skills and attention to detail, with a commitment to delivering high-quality training solutions tailored to the needs of machinery manufacturing.
• Familiarity with machining processes, CNC technologies, and machine tool operations is highly advantageous.

Job Purpose

The QA Engineer is responsible for ensuring product quality, compliance, and continuous improvement within AMI coating production. 

This role supervises QA Technicians in carrying out quality inspections, oversees quality data collection and reporting, manages customer feedback, and drives improvement initiatives. 

The QA Engineer also supports new project development and Quality & Environmental Management Systems (QEMS) to meet organizational goals. 

Responsibilities

1. Quality Assurance & Inspection

• Supervise QA Technicians to perform Outgoing Quality Assurance (OQA) inspections for shipment release.

• Ensure inspection processes are executed accurately and in compliance with established standards and requirements.

• Ensure proper control is exercised for identification, segregation, disposition and documentation of all non-conforming materials and products in coating production.

2. Data Collection & Reporting

• Collect, monitor, and analyze coating production yield data.

• Prepare and submit weekly quality and yield reports to management.

3. Continuous Improvement

• Initiate and lead continual improvement and lean projects to enhance quality, efficiency, and process reliability.

• Identify recurring quality issues and implement corrective and preventive measures.

4. Corrective Action Process

• Conduct failure analysis for both internal quality issues as well as customer feedback.

• Follow up Production’s corrective action report before closure.

• Record and track production customer’s feedback/complaint.

5. Project & Document Support

• Support new project development by preparing and implementing Quality Plans, Standard Operating Procedures (SOP), Standard Inspection Plans

• (SIP), and Work Instructions (WI).

• Collaborate with cross-functional teams to integrate quality requirements into project activities.

6. Measurement

• Monitor daily measurement results and analyze measurement deviation.

• Manage measurement equipment: Arrange for calibration and maintenance.

7. Engineering Change Process

• Track Engineering Change Request report.

• Validate changes as per ECR.

• Track and check on first 3 lots batch production upon completion of ECR.

8. QEHS Support

• Support the Quality & Environmental Management Systems (QEMS) by monitoring quality and environmental performance targets and programs.

• Ensure compliance with ISO and other regulatory requirements.

• Ensure proper control is exercised in production as per QEMS requirements and strive to achieve QEMS and Safety objectives.

9. Key Performance Indicators (KPI)

• Coating production yield

• CONQ

• Customer complaint rate and response time

• Internal quality deviations

• Zero nonconformance at internal and external ISO audit.

•   Initial and complete at least 1 lean project per quarter.

Requirements

• Bachelor Degree in Engineering/ Science

• Good documentation skills.

•   Knowledge of quality assurance methodologies, tools, and techniques

• Familiarity with ISO 9001 and ISO 14001, 2015 standards

• Experience in coating, surface treatment, or manufacturing industry is an advantage.

• Strong data analysis and reporting skills, with proficiency in MS Office (Excel, PowerPoint, Word).

• Ability to prepare and review Quality Plans, SOPs, SIPs, and Work Instructions.

• Understanding of lean manufacturing and continual improvement methodologies (Kaizen, 5S, Six Sigma).

• Comfortable working on-site (Monday - Friday).

This role is responsible to drive compliance and quality programs for Healthcare Transportation & Facilities and supporting the Healthcare Quality Management System to ensure processes and systems are compliant with regional and local regulations and customer requirements.

Responsibilities:

1. Quality Policies & Procedures:

Determine, implement & promote policies and procedures for Company’s Network and facilities (hubs & stations) to ensure compliance to standards such as GDP, GCP and others

2. Quality Assessment & Standards:

Write & review SOPs and Work Instructions for transportation & fulfilment solutions pertaining to the healthcare industry

3. Compliance & Quality Program Management:

Implement compliance and quality programs to support local Quality teams to ensure they are kept up-to-date and prepared.

4. CAPA Process Management:

Lead in process creation and review of documentation on the implementation and responses to corrective and preventive actions (CAPAs) and monitor action progress until closure.

5. Healthcare Quality Management System:

Develop, implement & support the system and processes, develop corresponding training programs, and acts as Super User for eQMS system.

6. Internal Audit Programs:

Provide inputs to support the design & implementation of robust internal audit processes to ensure readiness of various functions & processes when meeting regulatory agencies & customer audits

7. Certification Audits:

Lead and support various certification audits with relevant regulatory agencies and certification providers for the depot.

8. Operations & Customer Audit Programs:

Lead regular audit programs / random checks to achieve successful audit outcomes and proper post audit follow up actions.

9. Healthcare Customer Liaison:

Liaise with customers to understand quality requirements / issues / underlying concerns to advise on the way forward, provide advice based on interpretations as applicable to 3PL and support in issue resolution via conducting root cause analysis (depot).

10. Healthcare Quality Feedback:

Liaise, consolidate feedback from different functions to update and prepare final copy for Quality Questionnaires, Agreements and RFQ Proposals for customers.

11. Validation Programs:

Lead and support validation of transportation lanes and critical equipment like cold chain facilities, and packaging systems

Requirements :

• Hold local pharmacist license

• Have 3-5 years of relevant experience in pharmaceutical or healthcare industry in a quality related role

• Have competencies in quality assurance / regulatory affairs, customer relationship management and root cause analysis

• Have working experience ensuring compliance in accordance to Goods Manufacturing Practise cGMP,)/, Good Clinical Practises cGCP, Goods Distribution Practice (GDP) for Medical Devices and other local certifications in a warehouse and transportation business.

• IATA CEIV will be desired but not necessary.

• Familiar with drugs control and secondary labelling system

• Experience in conducting external and internal audits

• Must hold at least Bachelor’s degree in Pharmacy from a reputable local institute.

Working hours:

Mon to Fri 9am-6pm

Job Summary / Purpose

• Lead and maintain Quality Management System (QMS) aligned with ISO 9001, ISO 22000, ISO 13485

• Ensure compliance with GMP, GDP, FDA, EU regulations, China GB and other applicable standards

• Drive quality assurance across incoming, in-process & outgoing controls

• Support audits, regulatory compliance, and customer requirements

Responsibilities and Accountabilities:

• Quality Operations

· Establish and maintain QA inspection procedures

· Manage non-conformance and corrective actions (8D, RCA)

· Perform SPC, trend analysis, and risk assessment (FMEA)

• QMS & Compliance

· Maintain ISO 9001, ISO 22000, ISO 13485 systems

· Ensure GMP, GDP compliance

· Control SOPs and documentation

• Audit Management

· Conduct internal audits and follow up CAPA

· Support external certification audits

· Handle customer audits and responses

· Perform supplier audits and qualification

• Regulatory Compliance

· Ensure compliance with FDA, EU, China GB requirements.

· Support documentation such as DoC, SDS, and reports.

• Management Review & Improvement

· Prepare management review data and reports.

· Drive continuous improvement and Lean initiatives.

• Customer Management

· Handle customer complaints and quality communication.

• People Management

· Train and supervise QA Inspectors

· Manage QA Engineers (For Senior QA)

Requirement

• Degree in Engineering (Mechanical, Materials, Chemical, or related field)

• Certified Internal Auditor (ISO 9001 / ISO 22000 / ISO 13485)

• Certified Quality Engineer (CQE) or equivalent

• Minimum 2–5 years (QA Engineer)

• Minimum 5–8 years (Senior QA Engineer, with leadership experience)

• Experience in manufacturing (packaging, food, medical, or related industries preferred)

• Preferably able to start work immediately or at short notice

• Strong knowledge of :

1. QMS standards (ISO 9001, ISO 22000, ISO 13485)

2. GMP, GDP, and regulatory frameworks

3. SPC, FMEA, CAPA

4. Root Cause Analysis (8D)

5. Data analytics and reporting

6. Good understanding of manufacturing processes

7. Strong communication and audit handling skills

8. Ability to lead cross-functional teams

Job Summary

Responsible for management of Asia Quality System, Policies, Programs and Initiatives. Part of the Global Quality Team to maintain global quality system and drive global initiative.

Role and Responsibilities

Quality System

1. Develop, implement and maintain QMS documentation to maintain compliance with applicable standards such as ISO 9001, ISO 13485 or GMP

2. Monitor regulatory changes and update the QMS accordingly

3. Conduct internal audits and support external audits (external auditing bodies, suppliers and customers)

4. Analyze quality data and metrics to identify trends and areas for improvement

5. Collaborate with cross functional teams to ensure that the quality standards are integrated into processes

Management Representative

1. Reports on QMS performance to top management and recommend improvement

2. Point of contact for certification bodies

3. Lead Management Review and follow up action items

Product Quality Management

1. Analyze and capture recurring product complaints, collaborate with Operation and Technology teams to address compound specified failures

2. Operational Quality Support. To facilitate continuous improvement initiatives, by providing on the floor support through use of quality tools and coaching teams to build ownership and proactive engagement with quality processes.

Customer Complaints Management

1. CCAR Manager. Manage the customer complaints handling process to ensure that all complaints are logged with right information for investigation till auditing process

2. Collaborate with cross functional team during the investigation, resolution and communication of customer complaints

3. Review interim CCAR reports to ensure that root cause is data driven and corrective action(s) address the root cause

Supplier Complaints Management

1. SCAR Manager. Approve SCAR – Supplier related complaints and defects, review and monitor the effectiveness of corrective actions

2. Collaborate with Procurement, Supplier and internal stakeholders to investigate issues and resolution

3. Collaborate with Procurement, Operation and Technology to assess risk and quality impact of raw material on finished goods

Global Quality Team Collaboration

1. Support the implementation of global quality initiatives, systems and tools

2. Ensure that local QMS aligns with global practices and corporate policies

3. Share best practices and lessons learned across global sites

Support Quality Contracts/Documentation

1. Review customer documents and quality related agreements for compliances to ensure clauses are relevant, assess the risks.

2. Response to customer request for certifications, compliance/quality related/audit documents

System

1. Conduct training for staff in Quality Procedure, Standards and Tools.

2. Lead processes identified by the Global Quality Team such as PPAP, QIR, CCAR, SCAR and Mastercontrol for the Asia Region

Requirements:

· Degree or equivalent experience in a field of study such as chemistry, business, accounting, engineering, etc.

· Certificate in Quality Engineering is preferred.

· 4-6 years of quality management experience. Junior with 1-2 experience in related field can also apply

· Demonstrates introductory understanding and ability and with guidance, applies competency in typical situations.

· Able to design quality systems to meet customer expectations and internal needs. New approaches and continuous improvement must be ongoing.

· Good experience into customer & supplier audit and able to conduct training

· Good interpersonal skills to be able to communicate and collaborate with all stakeholders and deal with situation proactively

· Occasionally overseas travel and weekly conference call is required for the role

· This position required to communicate closely with vendors in China.

Working hours:

Mon to Fri 8.30am - 5.30pm ( 1 day hybrid )

Responsibilities:

1. Responsible for the end-to-end setup of the process quality module for the new factory;

2. Responsible for monitoring quality objectives during project trial production and mass production, and collecting issues;

3. Responsible for organizing Quick Response Quality Control (QRQC) meetings and handling non-conforming products;

4. Responsible for monitoring the progress of quality issue analysis and resolution, and escalate issues in a timely manner based on the current situation;

5. Responsible for updating and maintaining on-site Control Plans (CP) and Standard Inspection Procedures (SIP);

6. Responsible for leading customer audits and following up on identified issues;

7. Responsible for onboarding training for quality control inspectors.

Requirements:

1. 5+ years of work experience in the field of quality (including 2+ years of work experience in process quality); Experience in the automotive industry is preferred;

2. Possess IATF internal auditor qualification;

3. Be proficient in the five core quality tools in the automotive industry (APQP, PPAP, FMEA, MSA, SPC);

4. Experience in the end-to-end setup of a factory is preferred.

Position Summary

This position play a critical role in driving compliance and quality programs for Healthcare Transportation & Facilities and supporting the Healthcare Quality Management System to ensure processes and systems are compliant with regional and local regulations and customer requirements.

Job Scope

1. Quality Policies & Procedures: Determine, implement & promote policies and procedures for company’s Network and facilities (hubs & stations) to ensure compliance to standards such as GDP, GCP and others.

2. Quality Assessment & Standards: Write & review SOPs and Work Instructions for transportation & fulfilment solutions pertaining to the healthcare industry.

3. Compliance & Quality Program Management: Implement compliance and quality programs to support local Quality teams to ensure they are kept up-to-date and prepared.

4. CAPA Process Management: Lead in process creation and review of documentation on the implementation and responses to corrective and preventive actions (CAPAs) and monitor action progress until closure.

5. Healthcare Quality Management System: Develop, implement & support the system and processes, develop corresponding training programs, and acts as Super User for eQMS system.

6. Internal Audit Programs: Design & implement robust internal audit processes to ensure readiness of various functions & processes when meeting regulatory agencies & customer audits.

7. Certification Audits: Lead various certification audits with relevant regulatory agencies and certification providers across the region.

8. Operations & Customer Audit Programs: Lead & prepare for regular audit programs / random checks / regulatory activities to achieve successful audit outcomes and proper post audit follow up actions.

9. Healthcare Customer Liaison: Liaise with customers to understand quality requirements / issues / underlying concerns to advise on the way forward, provide advice based on interpretations as applicable to 3PL and resolve issues via conducting root cause analysis.

10. Healthcare Quality Feedback: Liaise, consolidate feedback from different functions to update and prepare final copy for Quality Questionnaires, Agreements and RFQ Proposals for customers.

11. Validation Programs: Lead the validation of transportation lanes and critical equipment like cold chain facilities, and packaging systems.

12. Depot Support: Provide secondary / backup support to healthcare specialists for market depots.

Requirements :

1. Hold local pharmacist license

2. Have at least 5 -7 years of relevant experience in warehouse, quality + QMS for pharmaceutical / healthcare industry in quality related role

3. Experience working in warehouse is desire

4. Have competencies in quality assurance / regulatory affairs, customer relationship management and root cause analysis

5. Have working experience ensuring compliance in accordance to Goods Manufacturing Practise cGMP,)/, Good Clinical Practises cGCP, Goods Distribution Practice (GDP) & ISO13485 for Medical Devices,

6. Experience in local certifications in a warehouse and transportation business.

7. IATA CEIV certification knowledge would be at advantage but not necessary.

8. Experience in conducting external and internal audits for regions

9. Must hold at least Bachelor’s degree in Pharmacy from a reputable local institute in Singapore.

10. Occasionally travel is required to sites and region warehouses.

Competency

1. Accuracy & attention to detail which is crucial to proper compliance to regulatory and standards

2. Problem-solving skills to support customer issue resolution

3. Planning & organization skills to ensure proper audit programs are managed effectively

4. Communication skills to facilitate engagements with customer and regulatory agencies

5. Project management capabilities and familiarity with Process Mapping, Six Sigma, Lean Methodology, Agile or Design Thinking

6. Apply data-driven decision making with the use of data analytics and visualization tools like Power BI and competency in Microsoft Office applications like Excel, Word, and PowerPoint

Working hours:

Mon to Fri 9am-6pm

Key Responsibilities

Develops and applies quality standards in accordance with company and customer requirements. Develops and conducts related tests.

Designs and implements methods and procedures for inspecting, testing, and evaluating the precision and accuracy of products and/ or production equipment.

Develops methods and parameters, project methodology and/ or project proposals.

Develops and uses procedures.  Prepares documentation for inspection/ testing procedures. Recommends corrective action for procedural, product, or process deficiencies.

Analyze operational data; Develop and implement recommendations.  Participates in and may lead audits. 

Evaluates work methods, procedures and policies. Tracks progress of qualification status, reviews reliability test results, determines disposition of non-compliant products, reviews and releases qualification packs 

Utilizes drawings, specifications, industry standards, and sketches, adapting inspection measuring devices and procedures when necessary. Read and interpret technical drawings and specification requirements.

Reduces qualification cycle time and cost while still meeting quality performance requirements. 

Functional Knowledge

• Demonstrates conceptual and practical expertise in own discipline and basic knowledge of related disciplines

Business Expertise

• Has knowledge of best practices and how own area integrates with others; is aware of the competition and the factors that differentiate them in the market

Leadership

• Acts as a resource for colleagues with less experience; may lead small projects with manageable risks and resource requirements

Problem Solving

• Solves complex problems; takes a new perspective on existing solutions; exercises judgment based on the analysis of multiple sources of information

Impact

• Impacts a range of customer, operational, project or service activities within own team and other related teams; works within broad guidelines and policies

Interpersonal Skills

• Explains difficult or sensitive information; works to build consensus

Job Description

We are seeking an experienced Test Manager to join our dynamic team in Singapore. In this pivotal role, you will lead and oversee all testing activities, ensuring the delivery of high-quality software products that meet our clients' expectations.

• Develop and implement comprehensive testing strategies, plans, and processes to ensure thorough testing coverage.
• Manage and mentor a team of skilled testers, providing guidance, training, and support to enhance their skills and performance.
• Collaborate closely with cross-functional teams, including developers, business analysts, and project managers, to align testing efforts with project requirements and timelines.
• Analyze and prioritize defects, ensuring timely resolution and effective communication with stakeholders.
• Continuously evaluate and improve testing processes, tools, and methodologies to enhance efficiency and effectiveness.
• Monitor testing progress, identify risks, and provide regular status updates to project stakeholders.
• Ensure compliance with industry standards, best practices, and internal quality assurance guidelines.

Qualifications

• Due to project sensitivity, we can only consider Singapore Citizen
• Proven experience as a Test Manager or a similar leadership role in software automation testing.
• Strong background in software testing methodologies, processes, and tools.
• Excellent analytical and problem-solving skills with a keen eye for detail.
• Proficient in test management tools (e.g., TestRail, qTest) and automation frameworks.
• Solid understanding of Agile/Scrum methodologies and their application in testing.
• Strong communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams.
• Bachelor's degree in Computer Science, Engineering, or a related field.
• Certification in software testing (e.g., ISTQB, CSTE) is preferred.
• Domain expertise in the relevant industry is a plus.

Salary: up to $9000

Working Days & Hours: Mon-Fri Office Hours

Location: Raffles Place

Job Description:
The registered data protection officer

Responsible for developing & maintaining APAC country specific compliance policy and process documents, training materials, providing help and guidance and awareness to APAC based employees.

Ensuring that all data protection/security/ HSE issues from audits or risks raised are recorded, with ownership, and tracking remediation tasks to closure/mitigation/acceptance of risks.

Management of the annual risk assessment program covering information security, data protection, health & safety, environment, and social governance

Initiate yearly compliance activities, eg. BCP exercise, call tree test, updating of various operations / compliance documentations, vendor due diligence exercise

Creation and maintenance of the Legal Risk Register (APAC)

Annual site audits and management of any remediation plans (H&S/Fire/Infosec/Data Protection/ESG)

Gathering of carbon emission data in support of global ESG reporting requirements

Attendance at the monthly country and compliance circle meetings

Responding to client information security assessments. Full completion and response to all Client questionnaires, including existing clients and new business opportunities.

Incident investigation and reporting pertaining to data and HSE

Development of the Quality Management System in support of attaining certification to ISO9001

Administrative tasks including but not limited to: Client sales bid compliance assistance, contract reviews (Data protection terms), uploading documents to client portals

Reviewing, updating and development of compliance policies and procedures

Job Requirements: Min Degree in finance/accountancy w min 3 yrs of relevant experience, preferably in financial sector

Interested candidates, please submit your resume to: allylok@recruitexpress.com.sg

Ally Audrey Lok Xin Woon

Recruit Express Pte Ltd (Healthcare & Lifescience)

Company EA Licence number : 99C4599

Personnel EA License: R21102307

allylok@recruitexpress.com.sg

We are seeking a responsible and hardworking individual to join our team as a Pest Control Technician. No prior experience is required — full training will be provided. This role involves learning how to carry out pest control services, maintaining high service standards, and ensuring compliance with safety and regulatory requirements.

Key Responsibilities:

• Assist in performing pest control treatments at customer sites.
• Learn to use pest control equipment and chemicals safely and effectively.
• Support routine inspections and help identify pest issues.
• Maintain proper documentation of services provided.
• Ensure compliance with NEA and safety guidelines at all times.

Requirements:

• No prior experience required — training will be provided.
• Willingness to learn and work in a hands-on environment.
• Responsible, hardworking, and safety-conscious.
• Good communication skills and ability to work in a team.
• Class 3/3A and 2 driving licence an advantage but not mandatory.

Why Join Us?
✔ Full training provided
✔ Career growth opportunities
✔ Supportive team environment

• Working Location: Woodlands
• Working Days: Monday – Friday
• Working Hours: 9:00am -6:00pm
• Starting Salary: $3,500 to $5,000

Responsibilities:

• Architect and design embedded firmware for motion control systems with a focus on optimal performance and precision
• Develop end-to-end application and firmware solutions including multi-thread, scheduling optimization, real-time operating systems (RTOS), and bare-metal implementations
• Design custom kernel drivers and APIs specifically tailored for motion control applications and interfacing with sensors and actuators
• Actively contribute to system architecture development and the implementation of new features relevant to motion control
• Design, develop, and thoroughly test firmware for embedded motion control systems
• Stay abreast of emerging technologies and advancements in motion control for product development enhancements
• Undertake debugging, system bring-up, beta testing, and production software development tasks
• Collaborate effectively with both software and hardware teams to ensure successful integration of motion control systems

Key Requirements:

• Bachelor's Degree in Computer Science, Electrical Engineering, or related field
• Minimum of 5 years of relevant experience in embedded software development
• Proficiency in software design and programming in C/C++ for development, debugging, testing, and performance analysis
• Understanding of hardware functionalities including clock-level issues, interrupts, polling, etc.
• Experience with motion controller systems, such as PID control loops, servo control algorithms, and interfacing with sensors and actuators for motion control applications

The Supreme HR Advisory Pte. Ltd || 14C7279

Chua Jie Ying (Cai Jie Ying), Evelynn || EA Personnel License R24120580