2,105 Quality Systems jobs in Malaysia

As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people’s lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology. We believe that the potential of great people, purpose-driven innovation, and world-class products can shape the future direction of healthcare. Teleflex is the home of Arrow, Barrigel, Deknatel, QuikClot, LMA, Pilling, Rüsch, UroLift and Weck – trusted brands united by a common sense of purpose. At Teleflex, we are empowering the future of healthcare. For more information, please visit teleflex.com.

Global Operations - Global Operations is a complex and diverse organization within the company which is responsible for product fulfilment to all our customers from end to end. We pride ourselves on being totally Customer Centric in our unrelenting focus on Improving Quality, Service and Value as perceived by our customers. Our employees are dedicated to the Global Operations Enterprise Excellence journey. Join a dynamic, growing team that offers healthcare providers an array of medical technology solutions that make a difference in patients’ lives.

1. Ensure compliance to Quality System Regulation (QSR), MDSAP, ISO 13485: 2016, MDD or EU MDR, Malaysia MDR and GDPMD, and Other Site Standards.
2. Management of Complaint Handling System, CAPA System and Internal Audit System.
3. Management of Document Control System.
4. Responsibility for Quality Management Review at Site, Regional and Global Level (as required).
5. Alignment of Corporate and Site Quality System Procedures.
6. Support and Site Representative of Quality System Global Harmonization Projects (as required).
7. Where appropriate, provide relevant Quality support in achieving Site Operational, Finance and Continuous Improvement Goals.
8. Reporting of relevant Quality Metrics to Senior Management.
9. Appointed designee for facility quality management representative.
10. To ensure the implementation and maintenance, within the department, of an effective management for occupational safety and health consistent with the Occupational Safety and Health Act 1994 and other legislative requirements.
11. Responsible for calibration of monitoring and measuring equipment on site.

Qualification : Degree in Engineering, Science or related discipline.
Experience : Minimum 5 years’ experience in Quality Management Systems (ideally within the Medical Device Industry)

Note: As with all positions, due to the dynamic nature of Teleflex Medical business, key responsibilities may evolve and change over time.

Teleflex is an equal opportunities employer.

At Teleflex, we follow a comprehensive hiring process. We do not accept unsolicited resumes from agency recruiters or 3rd party firms. We do not make unsolicited job offers. We do not ask for money or require equipment purchase up-front.

Expected Travel: None

Requisition ID: 12580

About Teleflex Incorporated

As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people's lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology. We believe that the potential of great people, purpose-driven innovation, and world-class products can shape the future direction of healthcare. 

Teleflex is the home of Arrow, Barrigel, Deknatel, QuikClot, LMA, Pilling, Rüsch, UroLift and Weck – trusted brands united by a common sense of purpose.

At Teleflex, we are empowering the future of healthcare.  For more information, please visit

Global Operations - Global Operations is a complex and diverse organization within the company which is responsible for product fulfilment to all our customers from end to end. We pride ourselves on being totally Customer Centric in our unrelenting focus on Improving Quality, Service and Value as perceived by our customers. Our employees are dedicated to the Global Operations Enterprise Excellence journey. Join a dynamic, growing team that offers healthcare providers an array of medical technology solutions that make a difference in patients' lives.

1. Ensure compliance to Quality System Regulation (QSR), MDSAP, ISO 13485: 2016, MDD or EU MDR, Malaysia MDR and GDPMD. and Other Site Standards.
2. Management of Complaint Handling System, CAPA System and Internal Audit System.
3. Management of Document Control System.
4. Responsibility for Quality Management Review at Site, Regional and Global Level (as required).
5. Alignment of Corporate and Site Quality System Procedures.
6. Support and Site Representative of Quality System Global Harmonization Projects (as required).
7. Where appropriate, provide relevant Quality support in achieving Site Operational, Finance and Continuous Improvement Goals.
8. Reporting of relevant Quality Metrics to Senior Management.
9. Appointed designee for facility quality management representative.
10. To ensure the implementation and maintenance, within the department, of an effective management for occupational safety and health consistent with the Occupational Safety and Health Act 1994 and other legislative requirements.
11. Responsible for calibration of monitoring and measuring equipment on site.

Note: As with all positions, due to the dynamic nature of Teleflex Medical business, key responsibilities may evolve and change over time.

Teleflex is an equal opportunities employer.

At Teleflex, we follow a comprehensive hiring process. We do not accept unsolicited resumes from agency recruiters or 3rd party firms. We do not make unsolicited job offers. We do not ask for money or require equipment purchase up-front.

Teleflex, the Teleflex logo, Arrow, Barrigel, Deknatel, QuikClot, LMA, Pilling, Rüsch, UroLift and Weck are trademarks or registered trademarks of Teleflex Incorporated or its affiliates, in the U.S. and/or other countries. 
2025 Teleflex Incorporated. All rights reserved.

Date: 26 Sept 2025

Location: Kamunting, 08, MY

Company: Teleflex

Expected Travel: None

Requisition ID: 12580

About Teleflex Incorporated

As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people's lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology. We believe that the potential of great people, purpose-driven innovation, and world-class products can shape the future direction of healthcare.

Teleflex is the home of Arrow, Barrigel, Deknatel, QuikClot, LMA, Pilling, Rüsch, UroLift and Weck – trusted brands united by a common sense of purpose.

At Teleflex, we are empowering the future of healthcare. For more information, please visit

Global Operations - Global Operations is a complex and diverse organization within the company which is responsible for product fulfilment to all our customers from end to end. We pride ourselves on being totally Customer Centric in our unrelenting focus on Improving Quality, Service and Value as perceived by our customers. Our employees are dedicated to the Global Operations Enterprise Excellence journey. Join a dynamic, growing team that offers healthcare providers an array of medical technology solutions that make a difference in patients' lives.

Position Summary

Principal Responsibilities

1. Ensure compliance to Quality System Regulation (QSR), MDSAP, ISO 13485: 2016, MDD or EU MDR, Malaysia MDR and GDPMD. and Other Site Standards.
2. Management of Complaint Handling System, CAPA System and Internal Audit System.
3. Management of Document Control System.
4. Responsibility for Quality Management Review at Site, Regional and Global Level (as required).
5. Alignment of Corporate and Site Quality System Procedures.
6. Support and Site Representative of Quality System Global Harmonization Projects (as required).
7. Where appropriate, provide relevant Quality support in achieving Site Operational, Finance and Continuous Improvement Goals.
8. Reporting of relevant Quality Metrics to Senior Management.
9. Appointed designee for facility quality management representative.
10. To ensure the implementation and maintenance, within the department, of an effective management for occupational safety and health consistent with the Occupational Safety and Health Act 1994 and other legislative requirements.
11. Responsible for calibration of monitoring and measuring equipment on site.

Education / Experience Requirements

Qualification : Degree in Engineering, Science or related discipline.

Experience : Minimum 5 years' experience in Quality Management Systems (ideally within the Medical Device Industry)

Specialized Skills / Other Requirements

Note: As with all positions, due to the dynamic nature of Teleflex Medical business, key responsibilities may evolve and change over time.

Teleflex is an equal opportunities employer.

At Teleflex, we follow a comprehensive hiring process. We do not accept unsolicited resumes from agency recruiters or 3rd party firms. We do not make unsolicited job offers. We do not ask for money or require equipment purchase up-front.

Teleflex, the Teleflex logo, Arrow, Barrigel, Deknatel, QuikClot, LMA, Pilling, Rüsch, UroLift and Weck are trademarks or registered trademarks of Teleflex Incorporated or its affiliates, in the U.S. and/or other countries.

2025 Teleflex Incorporated. All rights reserved.

Position Summary

This role is responsible for leading and coordinating the Quality Assurance (QA) and Quality Systems functions within a PCB and electronic components manufacturing environment. The position ensures that all products comply with customer requirements, regulatory standards, industry certifications, and HQ Shenzhen expectations.

The successful candidate will oversee QA operations (incoming, in-process, FQA, supplier quality, customer complaints) and drive QMS compliance across multiple standards (ISO 9001, IATF 16949, VDA 6.3, ISO 14001, etc.). The role also requires spearheading continuous improvement initiatives, managing audits, and serving as the company's representative for quality matters with customers, suppliers, and certification bodies.

Key Responsibilities

Quality Leadership & Operations

• Lead and oversee the QA department, including Incoming, In-Process, and Final Quality Assurance (FQA) operations.
• Align QA operations with corporate HQ policies and technical requirements.
• Ensure effective root cause analysis and corrective actions for customer complaints and internal non-conformances.
• Drive continuous improvement initiatives such as Six Sigma, Lean, and Kaizen to reduce defects and uplift quality performance.
• Provide monthly reporting on QA performance, KPIs, and customer quality metrics to both local management and HQ.
• Serve as the quality representative in key production, customer, and supplier meetings.

Quality Systems (QMS) & Compliance

• Maintain and enhance the company's Quality Management System (QMS) in alignment with:
  
  i. VDA 6.3 – Process Audit Standard (automotive industry)
  
  ii. IATF 16949 – Automotive QMS
  
  iii. AS9100 – Aerospace QMS
  
  iv. ISO 9001 – General Quality Management Systems
  
  v. ISO 14001 – Environmental Management Systems
  
  vi. ISO 13485 – Medical Devices Quality Management Systems
  
  vii. ISO 45001 – Occupational Health & Safety Management Systems
  
  viii. Ecovadis – Sustainability & CSR Rating
  
  and other customer-specific standards.
• Develop, review, and update quality policies, SOPs, and work instructions.
• Support the preparation of quality documentation including Control Plans, FMEA, PPAP, APQP, and MSA.
• Ensure calibration and maintenance of inspection and testing equipment.
• Participate in internal audits, supplier evaluations, customer audits, and certification audits.

Supplier & Customer Quality

• Manage supplier quality performance and incoming material inspections.
• Ensure effective handling of customer complaints and corrective actions.
• Support customer quality reporting and coordinate with HQ on quality system improvements.

Team Development & Training

• Ensure QA staff are trained in quality tools, systems, and standards.
• Provide mentorship and technical guidance to QA team members.
• Foster a culture of quality awareness and accountability across all departments.

Requirements

• Bachelor's Degree in Engineering, Quality Management, or related discipline (Diploma acceptable for coordinator role).
• QA Manager: Minimum 5 years' experience in QA, with at least 3 years in a managerial role,preferably in PCB or EMS manufacturing.
• Must know well of ISO 9001, IATF 16949, VDA 6.3, ISO 14001, and electronics/automotive/PCB industry standards.
• Proficient in quality tools: SPC, FMEA, MSA, APQP, 8D, PPAP.
• Excellent analytical, documentation, and reporting skills.
• Must be able to speak and write in Chinese (for HQ Shenzhen coordination).
• Good command of English and Malay.

**Job Description

• Coordinate internal audit activities such as QMS, 5S and etc.

• Support other audits such as ANSI/ESD S20.20 certification audit, customer audit, LEAN audit and etc.

• Coordinate and compile reports/presentation slides for management review.

• Coordinate on Calibration activities. Maintain Calibration and Preventive Maintenance System.

• Ensures the process being done is in compliance with the Deviation Authorization.

• Liaise with Certification body and Calibration Suppliers.

Requirements

• Degree in Electrical & Electronic / Mechanical Engineering

• At least 2-3 years working experience in an Electronics Manufacturing / Repair Environment

• Strong knowledge in ISO standards.

• Ability to manage certification processes with regulatory bodies.**

Lead and drive integration and sustainability for Global Quality Systems (ISO 9001) for the Malaysia sites and across the Asia region for Automotive (IATF 16949). This position is in Penang, Malaysia.

ESSENTIAL DUTIES AND RESPONSIBILITIES

• Implement and support the set-up of integrated quality systems for Global Quality for the Asia region for ISO 9001 and IATF 16949
• Support the Regional Site Operations Directors / Managers to drive deployment of all regional and global Quality System Initiatives.
• Create and manage a community of Quality Systems Management across the region, ensuring the use of best practices across all areas of Operations.
• Ensure that metrics (KPI) are accurately and effectively used to assess the continuing suitability, adequacy, and effectiveness of the quality management systems.
• Ensure that all sites employ the full range of quality systems development and problem-solving tools as required.
• Drive Global Quality Systems initiatives throughout the region of responsibility. Establish Quality as a competitive advantage.
• Mentor Site Quality Managers.
• Ensure quality system objectives are met in the region of responsibility.
• Create and manage a community of quality systems professionals and Subject Matter Experts.
• Drive Continuous Improvement mentality across all sites.
• Provide a path of escalation for all Site Quality/Systems Managers and Quality teams.
• Work synergistically with other Functional leads across Operations Development Team in region of responsibility.
• Provide reactive support to individual sites and businesses in the event of quality system issues and escalations.
• Provide leadership within the Quality Management community of region of responsibility.
• May perform other duties and responsibilities as assigned.

Build your career with Jabil! We challenge and empower you to make most of your talents, working with outstanding colleagues from diverse backgrounds who share your drive and passion to make Jabil grow!

Lead and drive integration and sustainability for Global Quality Systems (ISO 9001) for the Malaysia sites and across the Asia region for Automotive (IATF 16949). This position is in Penang, Malaysia.

• Implement and support the set-up of integrated quality systems for Global Quality for the Asia region for ISO 9001 and IATF 16949
• Support the Regional Site Operations Directors / Managers to drive deployment of all regional and global Quality System Initiatives.
• Create and manage a community of Quality Systems Management across the region, ensuring the use of best practices across all areas of Operations.
• Ensure that metrics (KPI) are accurately and effectively used to assess the continuing suitability, adequacy, and effectiveness of the quality management systems.
• Ensure that all sites employ the full range of quality systems development and problem-solving tools as required.
• Drive Global Quality Systems initiatives throughout the region of responsibility. Establish Quality as a competitive advantage.
• Mentor Site Quality Managers.
• Ensure quality system objectives are met in the region of responsibility.
• Create and manage a community of quality systems professionals and Subject Matter Experts.
• Drive Continuous Improvement mentality across all sites.
• Provide a path of escalation for all Site Quality/Systems Managers and Quality teams.
• Work synergistically with other Functional leads across Operations Development Team in region of responsibility.
• Provide reactive support to individual sites and businesses in the event of quality system issues and escalations.
• Provide leadership within the Quality Management community of region of responsibility.
• May perform other duties and responsibilities as assigned.

Knowledge Requirements

• Fluent in English and Mandarin required
• Excellent leadership skills.
• Effective communicator
• Practices humility and influencing at any level within the organization to achieve goals.
• Proficient and knowledgeable in quality management systems.
• Strong analytical skills.
• Results-driven change agent.
• Ability to communicate in all media forms and cross-culturally.
• Organizationally astute, but not politically motivated.
• Track record showing continual improvement of personal skills.
• Proficiency in use of personal computers, Microsoft Office products (Excel, Word and PowerPoint) and e-mail skills required.

Education & Experience Requirements

• Bachelor’s degree in Engineering, Science or Analytical discipline required.
• Experience as a Quality Manager / QMS Manager in high volume, high mix industries.
• Minimum of 7 years of relevant experience.
• Minimum of 5 years in SMT, and good knowledge of Machining, Tooling, and Plastic manufacturing process.
• 5 years of experience in management in a heavily matrixed environment.
• Proven experience implementing and sustaining Quality Management Systems for ISO 9001 and IATF16949
• Experienced in successfully leading the Quality System function in a multi-cultural and multi-site environment.
• Proven experience in developing and maintaining FMEAs and Control Plans
• Proven Certified Six Sigma Green or Black Belt preferred.
• Or a combination of education, experience and/or training.
• 25% travel required, domestic and international

Compensation Grade: M04

BE AWARE OF FRAUD: When applying for a job at Jabil you will be contacted via correspondence through our official job portal with a jabil.com e-mail address; direct phone call from a member of the Jabil team; or direct e-mail with a jabil.com e-mail address. Jabil does not request payments for interviews or at any other point during the hiring process. Jabil will not ask for your personal identifying information such as a social security number, birth certificate, financial institution, driver’s license number or passport information over the phone or via e-mail. If you believe you are a victim of identity theft, contact your local police department. Any scam job listings should be reported to whatever website it was posted in.