Total 728 quality manager job vacancies in Quality Assurance / Control category in Hong Kong

• 5-Day Work Week: Mondays – Fridays , 8:30am to 6:00pm

• Location: East

• Basic Salary: Up to S$4,200 (commensurate with experience)

• Industry: Healthcare

A leading healthcare provider is seeking a Quality Management Executive to support and drive quality improvement initiatives, patient safety standards, and regulatory compliance across its operations.

Job Responsibilities:

• Manage incidents, customer feedback and complaints, ensuring timely resolution and implementation of preventive measures

• Identify and assess risks to patient safety and quality of care

• Develop strategies to mitigate risks and enhance clinical quality and patient safety outcomes

• Monitor, analyse and evaluate data to assess effectiveness of quality programmes and initiatives

• Collaborate with internal stakeholders and external consultants to achieve and maintain certifications

• Support implementation of healthcare regulatory requirements, including data protection and health information policies

• Work with cross-functional teams to review and improve healthcare processes, workflows and procedures

• Track and maintain quality indicators (productivity, customer satisfaction, incidents, feedback) and prepare management reports

• Maintain document control and oversee organisation-wide documentation inventory

• Manage and track external correspondences with regulatory bodies

Job Requirements:

• Min. Diploma in any discipline

• Min. 3 years of relevant experience in quality management, preferably within the healthcare sector

• Experience in quality assurance, quality improvement, patient safety, and/or personal data protection

• Sound knowledge of statutory regulations and healthcare-related guidelines across all areas of healthcare operations

• Exposure to Root Cause Analysis (RCA) and Failure Modes and Effects Analysis (FMEA) will be advantageous

Looking for a change or a new challenge? Please email your detailed resume in MS Word format to cherry.cheng@celecti.com.sg

Cherry Cheng Wei (Ms.) | Talent Acquisition Consultant | CEI Reg. No: R26160225| Mobile no.: 89038330

Job Description & Requirements

The Quality System / QC Engineer is responsible for maintaining and improving the Quality Management System (QMS) and ensuring Product Quality through inspection, testing, and continuous improvement activities. The role ensures compliance with ISO 9001, ISO 14001, and ISO 45001 standards, customer requirements, and regulatory guidelines while supporting operational excellence.

________________________________________

Key Responsibilities

1. Quality Management System (QMS)

• Maintain and improve the Quality Management System in accordance with ISO 9001 / IATF 16949 / ISO 13485 (as applicable).

• Create and update Work Instructions, Procedures, Process Flow charts, Control Plans, and FMEA documents.

• Control and manage all QMS documents, including customer drawings, specifications, and procedures.

• Coordinate and conduct internal audits for ISO 9001, ISO 14001, and ISO 45001.

• Support customer audits and certification audits.

• Monitor corrective and preventive actions (CAPA) and ensure timely closure.

• Ensure compliance with customer-specific requirements.

• Cross-Functional Collaboration - Work closely with Planning, Production, R&D/Engineering Team

________________________________________

2. Quality Control (QC) Operations

• Supervise and manage QC Inspectors in their daily activities on the production floor.

• Establish and monitor incoming, in-process, and final inspection activities on the production floor.

• Review incoming, in-process, and final inspection reports, ensuring proper documentation and record retention in the system.

• Track and monitor in-coming and final outgoing product yield

• Manage non-conforming materials and disposition activities.

• Establish Statistical Process Control (SPC) and monitor process capability (Cp, Cpk).

• Analyze process data to identify trends, variations, and improvement opportunities.

• Drive root cause analysis and corrective actions report for process-related quality issues or customer complaints.

• Support new process introduction (NPI)

• Provide guidelines and training to QC Operators

Our client, a leading financial services firm, operates in a dynamic and fast-evolving environment where you will play a critical role in managing regulatory, business, and reputational risks across APAC. This is an excellent opportunity to work at the intersection of payments, digital assets (crypto), and regulatory compliance within a highly regulated and innovative landscape.

What You’ll Do

• Partner with senior management and business teams to provide regulatory and compliance advisory across APAC (Singapore, Malaysia, Australia, Japan)
• Advise on licensing requirements (e.g., Major Payment Institution, Digital Payment Token services) across multiple jurisdictions
• Drive policy and procedure enhancements in line with MAS and regional regulatory frameworks
• Oversee key compliance areas including:Regulatory change managementTechnology risk & outsourcingComplaints handling & compliance monitoringCross-border marketing & conflicts of interest
• Support business expansion and new product initiatives, especially in digital payments and crypto
• Conduct risk assessments and ensure mitigation frameworks are in place
• Manage audits, regulatory queries, and investigations
• Contribute to strategic projects, including digital platform enhancements

What We’re Looking For

• ~5+ years of experience in regulatory compliance / financial crime compliance within payments or financial services
• Strong knowledge of MAS regulations, especially around Major Payment Institution (MPI) frameworks
• Exposure to payments, e-money, remittance, or digital assets (crypto) is highly preferred
• Experience with regulators, banks, audit firms, or fintech environments

Qualifications

• Degree in Finance, Business, Law, Accounting, or related field
• Compliance certifications (e.g., CAMS, ICA) are a plus.

If you or anyone within your network would like to apply then do share your CV with Manisha@kstalentsolutions.com/ Komal@kstalentsolutions.com

• Serving as technical expert to support production and resolve manufacturing issues.
• Supporting engineering changes, deviation request, training, qualification and update procedures.
• Streamline process through supporting continuous improvement and automation implementation.
• Providing support on improvement activities through workflow and digital tools.
• Ad hoc duties

Requirements:

• Min Diploma in Engineering
• Min 1-2 years of experience in production/manufacturing
• Able to think out of the box with strong desire to learn and a great teammate.
• Good communication skills

Interested & qualified applicants, please forward your latest CV to fion@pnnacle.com.sg

Join a globally recognised specialty chemicals organisation with a strong footprint in innovation, sustainability, and high-performance ingredients. With decades of expertise and a collaborative culture, this company offers a stable and rewarding environment for individuals looking to build a long-term career in chemical manufacturing.

What You’ll Enjoy

• Competitive salary package: Up to $3,000 basic + $700 fixed allowances
• Additional overtime pay and meal allowances when extra hours are required
• Company transport provided at designated point for work location at Jurong Island
• Permanent role with AWS and Variable Bonus
• Structured training and development opportunities
• Exposure to international quality standards and advanced laboratory practices
• Supportive team environment within a reputable multinational company

Your Role

As a Quality Control Analyst, you will play a key role in ensuring product quality and compliance across the manufacturing process. Your responsibilities include:

• Conducting routine QC analysis on raw materials, in-process samples, and finished products to support production operations
• Accurately documenting and maintaining QC data in line with site QA standards
• Performing non-routine testing, including investigations related to customer or supplier feedback
• Handling equipment calibration and maintaining proper calibration records
• Collaborating with internal teams to ensure timely communication of results
• Supporting investigations for out-of-specification (OOS) results and ensuring proper documentation
• Adhering strictly to Safety, Health & Environment (SHE) and Quality Assurance procedures
• Contributing to a safe working environment for yourself and your team
• Assisting in onboarding and training of new team members

What We’re Looking For

• Background in Chemistry or Chemical Manufacturing (Diploma or Degree)
• Strong interest in laboratory work and quality assurance within a manufacturing setting
• Detail-oriented with the ability to follow procedures and analytical methods precisely
• Good communication skills and a team-oriented mindset
• Comfortable working on a permanent 12-hour day shift schedule
• Willingness to support overtime when required, especially during critical production periods

This opportunity is well-suited for individuals looking to gain hands-on experience in a structured manufacturing environment, including those at the early stages of their career or seeking to deepen their technical expertise.

Apply Now

Interested candidates are invited to submit their CV in MS Word format to: weiyan@triton-ai.com

Reg No.: R1983718
Triton AI Pte Ltd | EA License No.: 21C0661

Our client, a leading financial services firm, offers a dynamic environment where you will play a key role in managing regulatory, business, and reputational risks across APAC. This is an exciting opportunity to work across derivatives, securities, commodities, and FX within a highly regulated and fast-paced landscape.

Key Responsibilities

• Provide regulatory and compliance advisory to senior management and business units
• Ensure policies and controls align with MAS, SGX, SFC, and regional regulations
• Oversee key compliance areas including:Licensing & regulatory change managementTrade surveillance & market abuse.
• Derivatives reporting & compliance monitoringCross-border marketing, outsourcing & conflicts management
• Support business expansion, new products, and transaction advisory
• Conduct compliance risk assessments and drive mitigation strategies
• Manage audits, regulatory queries, and investigations
• Contribute to strategic and digital transformation projects

What We’re Looking For

• 5+ years of experience in regulatory compliance within financial services
• Strong exposure to derivatives (ETD/OTC), trading or capital markets
• Solid understanding of MAS regulations, SGX-DT rules, and APAC frameworks
• Background in banks, brokerages, or audit firms

Qualifications

• Degree in Finance, Business, Law, Accounting, or related field
• Compliance certifications are a plus

If you or anyone within your network is keen to explore this further then do share your CV with manisha@kstalentsolutions.com / Komal@kstalentsolutions.com

Responsibilities:

• Maintain accurate and up-to-date ISO 9001, ISO 14001, and ISO 13485 documentation, including Quality Manuals, procedures, work instructions, and records, to ensure system compliance and management review readiness.
• Plan, coordinate, and conduct internal and external audits to ensure organizational readiness for third-party certification, management reviews, and customer audits.
• Collaborate with internal stakeholders to support and participate in customer and supplier audits to ensure compliance requirements are met.
• Review audit findings, develop corrective action plans, and drive continuous improvement initiatives.
• Generate and review supplier quality performance reports, work closely with suppliers to resolve non-conformances, and promote continuous improvement.
• Issue, monitor, and follow up on Supplier Corrective Action Requests (SCAR), ensuring effectiveness and timely closure.
• Support qualification and onboarding of new suppliers to maintain a robust pipeline aligned with production requirements.
• Manage calibration schedules and preventive maintenance programs for equipment to ensure operational reliability and compliance.
• Address quality issues arising from production and customer feedback by working closely with production teams to implement corrective actions and resolve customer complaints with proper documentation.
• Ensure timely closure of Corrective and Preventive Actions (CAPA), non-conformance reports, and customer complaints, and publish quality performance reports.
• Lead Material Review Board (MRB) meetings with cross-functional teams to perform root cause analysis, implement corrective actions, and verify effectiveness.
• Supervise and lead QC inspectors to ensure parts inspection compliance with engineering drawings and quality standards.

Qualifications:

• Diploma in Quality Management, Engineering, Manufacturing, or a related field.
• Min 3 years of relevant experience in quality or manufacturing environments, with exposure to audits and documentation.
• Basic understanding of supplier management and quality coordination.
• Familiarity with commonly used quality management standards (e.g. ISO systems).
• Working knowledge of quality tools and process control methods.

We regret only shortlisted candidates will be contacted. All applications will be handled confidentially. By submitting your application, you agree to the collection, use, retention, and disclosure of your personal information to prospective employers.

Wecruit Pte Ltd

EA License No: 20C0270

EA Personnel: Nyon Hock Sen (Aden)

EA Personnel Reg No: R24124070

Responsibilities:

• Maintain accurate and up-to-date ISO 9001, ISO 14001, and ISO 13485 documentation, including Quality Manuals, procedures, work instructions, and records, to ensure system compliance and management review readiness.
• Plan, coordinate, and conduct internal and external audits to ensure organizational readiness for third-party certification, management reviews, and customer audits.
• Collaborate with internal stakeholders to support and participate in customer and supplier audits to ensure compliance requirements are met.
• Review audit findings, develop corrective action plans, and drive continuous improvement initiatives.
• Generate and review supplier quality performance reports, work closely with suppliers to resolve non-conformances, and promote continuous improvement.
• Issue, monitor, and follow up on Supplier Corrective Action Requests (SCAR), ensuring effectiveness and timely closure.
• Support qualification and onboarding of new suppliers to maintain a robust pipeline aligned with production requirements.
• Manage calibration schedules and preventive maintenance programs for equipment to ensure operational reliability and compliance.
• Address quality issues arising from production and customer feedback by working closely with production teams to implement corrective actions and resolve customer complaints with proper documentation.
• Ensure timely closure of Corrective and Preventive Actions (CAPA), non-conformance reports, and customer complaints, and publish quality performance reports.
• Lead Material Review Board (MRB) meetings with cross-functional teams to perform root cause analysis, implement corrective actions, and verify effectiveness.
• Supervise and lead QC inspectors to ensure parts inspection compliance with engineering drawings and quality standards.

Qualifications:

• Diploma in Quality Management, Engineering, Manufacturing, or a related field.
• Min 3 years of relevant experience in quality or manufacturing environments, with exposure to audits and documentation.
• Basic understanding of supplier management and quality coordination.
• Familiarity with commonly used quality management standards (e.g. ISO systems).
• Working knowledge of quality tools and process control methods.

We regret only shortlisted candidates will be contacted. All applications will be handled confidentially. By submitting your application, you agree to the collection, use, retention, and disclosure of your personal information to prospective employers.

Wecruit Pte Ltd

EA License No: 20C0270

EA Personnel: Nyon Hock Sen (Aden)

EA Personnel Reg No: R24124070

Duties & Responsibilities:

• Maintain and upkeep production/training/safety-related documentation.
• Maintain and upkeep receiving records/documents and request COAs from vendors.
• Coordinate with QA/QC department to ensure operation complies with food safety (e.g., FSSC/ISO) and all regulatory requirements (e.g., SFA).
• Ensure the retention samples arrangement, e.g., get from production, retention area arrangement, arrange to an external laboratory, and submit the analysis to QA for review.
• Assist in ensuring the products are traceable.
• Ensure production efficiency with minimal wastage.
• Assist in monthly pest control services.
• conduct daily inspection on receiving on raw materials, production, deliveries regulatory requirement add Halal
• Asist in food safety internal audit, customer audit, FSSC/ISO audit.
• Supporting in any ad-hoc duties as assigned by management from time to time.

Requirements:

• Minimum Diploma in Applied Science (Nutrition and Food Science) or related fields
• Basic food hygiene certification is an added advantage
• Minimum 1-year relevant working experience in food manufacturing
• Good interpersonal and communication abilities.
• Proficient in MS office e.g., Word, and Excel.

Working Hours:

• Monday to Friday – 8.30 am to 5.30 pm
• Saturday – 8.30 am to 12.00 pm

Transport provided from Kranji MRT Station

Lunch is provided in-house.

Responsibilities:

• Maintain and continuously improve the ISO 9001 quality management system, ensuring effectiveness across machining and sheet metal fabrication processes

• Plan and conduct internal quality audits, focusing on process compliance and effectiveness on the shop floor

• Lead, coach, and develop QA/QC inspectors to support in-process and final inspection activities

• Develop and implement inspection strategies and control plans aligned with tight tolerance machining and sheet metal fabrication requirements

• Interpret complex engineering drawings and ensure proper deployment of GD&T requirements into manufacturing and inspection processes

• Review and approve First Article Inspection (FAI) reports for new products and engineering changes

• Lead internal non-conformance management, including MRB activities, disposition (rework/repair/scrap), and validation of corrective actions

• Drive structured problem-solving (8D, 5 Whys) for internal quality issues, ensuring robust root cause identification and sustainable corrective actions

• Analyze quality data (scrap, rework, Cp/Cpk, yield trends) to identify systemic issues and drive continuous improvement

• Support New Product Introduction (NPI) to ensure manufacturability, inspection readiness, and quality risk mitigation

• Perform hands-on dimensional inspection for critical and complex features when required

• Drive shop-floor quality improvements, including mistake-proofing (poka-yoke) and standardization of best practices

• Take on additional responsibilities aligned with business and operational needs

Requirements:

• Diploma or Degree in Mechanical, Manufacturing, or related Engineering discipline

• Minimum 3 years of experience in a precision machining and/or sheet metal fabrication environment

• Proven hands-on experience with GD&T application and CMM inspection (FARO Arm / Fixed CMM)

• Experience handling tight tolerance components and complex geometries

• Practical experience in SPC, FMEA, and structured problem solving (8D)

• Strong working knowledge of ISO 9001 quality systems within precision machining and sheet metal environments

• Advanced GD&T proficiency (ASME Y14.5), with the ability to interpret complex drawings and support tolerance-related decisions

• Hands-on experience with CMM systems, including FARO Arm and fixed CMM, with capability in measurement execution, basic programming, and results interpretation

• Strong understanding of CNC machining (turning, milling) and sheet metal processes (laser cutting, bending, welding, finishing) and their impact on dimensional and cosmetic quality

• Proficiency in inspection techniques for tight tolerances, complex geometries, and formed components

• Solid knowledge of SPC, Cp/Cpk, FMEA, and control plans, with practical application on the shop floor

• Strong problem-solving capability, using structured methodologies such as 8D, 5 Whys, and Fishbone analysis

• Effective interpersonal and communication skills, with the ability to work cross-functionally with production, engineering, and quality teams

• Team-oriented, hands-on approach, comfortable operating in a fast-paced manufacturing environment

• High attention to detail with a practical, solution-focused mindset

Responsibilities:

• Maintain and continuously improve the ISO 9001 quality management system, ensuring effectiveness across machining and sheet metal fabrication processes

• Plan and conduct internal quality audits, focusing on process compliance and effectiveness on the shop floor

• Lead, coach, and develop QA/QC inspectors to support in-process and final inspection activities

• Develop and implement inspection strategies and control plans aligned with tight tolerance machining and sheet metal fabrication requirements

• Interpret complex engineering drawings and ensure proper deployment of GD&T requirements into manufacturing and inspection processes

• Review and approve First Article Inspection (FAI) reports for new products and engineering changes

• Lead internal non-conformance management, including MRB activities, disposition (rework/repair/scrap), and validation of corrective actions

• Drive structured problem-solving (8D, 5 Whys) for internal quality issues, ensuring robust root cause identification and sustainable corrective actions

• Analyze quality data (scrap, rework, Cp/Cpk, yield trends) to identify systemic issues and drive continuous improvement

• Support New Product Introduction (NPI) to ensure manufacturability, inspection readiness, and quality risk mitigation

• Perform hands-on dimensional inspection for critical and complex features when required

• Drive shop-floor quality improvements, including mistake-proofing (poka-yoke) and standardization of best practices

• Take on additional responsibilities aligned with business and operational needs

Requirements:

• Diploma or Degree in Mechanical, Manufacturing, or related Engineering discipline

• Minimum 3 years of experience in a precision machining and/or sheet metal fabrication environment

• Proven hands-on experience with GD&T application and CMM inspection (FARO Arm / Fixed CMM)

• Experience handling tight tolerance components and complex geometries

• Practical experience in SPC, FMEA, and structured problem solving (8D)

• Strong working knowledge of ISO 9001 quality systems within precision machining and sheet metal environments

• Advanced GD&T proficiency (ASME Y14.5), with the ability to interpret complex drawings and support tolerance-related decisions

• Hands-on experience with CMM systems, including FARO Arm and fixed CMM, with capability in measurement execution, basic programming, and results interpretation

• Strong understanding of CNC machining (turning, milling) and sheet metal processes (laser cutting, bending, welding, finishing) and their impact on dimensional and cosmetic quality

• Proficiency in inspection techniques for tight tolerances, complex geometries, and formed components

• Solid knowledge of SPC, Cp/Cpk, FMEA, and control plans, with practical application on the shop floor

• Strong problem-solving capability, using structured methodologies such as 8D, 5 Whys, and Fishbone analysis

• Effective interpersonal and communication skills, with the ability to work cross-functionally with production, engineering, and quality teams

• Team-oriented, hands-on approach, comfortable operating in a fast-paced manufacturing environment

• High attention to detail with a practical, solution-focused mindset

At Alcon, we're passionate about enhancing sight and helping people see brilliantly. With more than 25,000 associates, we innovate fearlessly, champion progress, and act swiftly to impact global eye health. We foster an inclusive culture, recognizing your contributions and offering opportunities to grow your career like never before. Together, we make a difference in the lives of our patients and customers. Are you ready to join us?

The Director, Quality Assurance is primarily responsible for developing and implementing strategies for quality oversight across all Affiliate sites within Alcon's Quality & Regulatory Affairs. You will ensure compliance with quality standards, manage quality events, and oversee complaint handling.

Specifics Include:

• Lead and direct teams to develop and implement strategies for departmental success and alignment with company goal
• Ensure compliance with quality standards and drive continuous improvement initiatives
• Manage departmental resources and make key decisions
• Guide non-conformance investigations with a structured approach to root cause analysis and problem-solving
• Lead audit preparation and manage external audits by Health Authorities and Notified Bodies
• Oversee all Quality-related activities at the country level, ensuring compliance with regulatory standards and global requirements
• Oversee quality control activities for finished products and handle product complaints
• Develop and oversee processes for an effective Quality System, includingself-inspections, supplier qualifications, corrective and preventive action (CAPA) processes, and Standard Operating Procedure (SOP) compliance
• Promote a strong Quality Culture and work closely with commercial partners and leadership teams to drive compliance as a strategic business platform
• Ensure compliance with market authorization, Good Manufacturing Practice(GMP), International Organization for Standardization (ISO) 13485, Good Distribution Practice (GDP), and local requirements
• Review and approve documentation for medicinal products and medical devices
• Ensure Good Practice (GxP) suppliers are qualified and monitored, and manage market actions
• Adhere to GxP regulations by following SOPs, maintaining accurate documentation, and completing required training
• Contribute to the overall compliance of the organization through individual job requirements
• Lead quality reviews with leadership teams, oversee key quality indicators at both country and regional levels, ensure each country’s quality plans align with regional and global standards, and managing escalations to the Global Quality Compliance function
• Oversees monthly quality performance by tracking and submitting KQI metrics, managing quality risk assessments, preparing reports for the CSCQ Head, and maintaining ongoing surveillance to support business continuity
• Oversee the end‑to‑end complaint handling operations, including timely intake, assessment, follow‑up, and routing of technical complaints and Adverse Events for all Alcon medical device products, ensuring compliance with local and international regulatory requirements
• Drive a strong quality and compliance culture across the region by promoting best practices, ensuring consistent application of complaint handling processes, and supporting continuous improvement of quality systems
• Lead and develop the complaint handling team, providing guidance on investigations, overseeing case triage, and managing escalations such as product replacements and refund requests to ensure efficient and accurate resolution
• Ensures strong people and capability development by driving talent development and succession planning, managing direct reports’ performance and compliance, overseeing training completion, and providing ongoing leadership and mentorship to the team
• This role also requires regular regional travel to support country teams, oversee activities, and ensure consistent implementation of quality standards
  

Education:                      Bachelor’s Degree in Life Sciences, Pharmacy, Engineering or other scientific discipline

Languages:                     English Proficiency

       Knowledge/ Fluency of at least one other language preferred

Experience:

• Minimum 15 years of experience in Quality Assurance, 10 years of people leadership in the medical device industry with people management experience in a matrix environment.
• Experience working in a multinational company or across multiple countries in the APAC region.
• Proven track record of developing and implementing quality assurance strategies and programs.
• Strong understanding of regulatory requirements and industry standards related to quality assurance (e.g., ISO 9001, ISO 13485, GMP, QSD and other industry standards that may apply).
• Excellent leadership and communication skills, with the ability to motivate and inspire teams to achieve quality objectives.
• Analytical mindset with strong problem-solving skills, able to lead root cause analysis and CAPA initiatives.
• Broad understanding of global expectations of Health Authorities in the GxP regulated area.
• Exposure to manufacturing operations and /or quality assurance, country organizations or commercial operations.
• Knowledge and experience in forecasting software and demonstrated proficiency in Microsoft suites.

Why join Alcon?

- Join a global leader with a rich history of innovation and excellence in eye care.

- Be part of a collaborative and supportive team culture that values diversity and inclusion.

- Enjoy a competitive compensation package and opportunities for career advancement.

- Make a meaningful difference in the lives of patients worldwide by contributing to cutting-edge advancements in eye health.

If you're ready to take the next step in your career and lead a dynamic team towards success, we want to hear from you! Apply now and join us in shaping the future of eye care at Alcon.

Alcon Careers

See your impact at alcon.com/careers

Job Description

As a Quality and Compliance Specialist, you will play a pivotal role in ensuring that all products and operations within Project WATT meet regulatory requirements and quality standards. This role focuses on managing product certification, conducting regulatory audits, and ensuring that operational processes align with local and international laws. Collaborating with technical and operational teams, you will safeguard compliance while driving continuous improvement in quality management.

Responsibilities

• Product Quality Compliance:

1. Ensure that all products (hardware and software) comply with relevant regulations and industry standards, such as TR25 for EV charging systems in Singapore.
2. Maintain and update product certifications and manage regulatory audits and inspections.
3. Review testing results and performance reports to verify adherence to quality standards.

• Operational Compliance:

1. Oversee business operations to ensure alignment with legal and regulatory requirements, such as data privacy and environmental standards.
2. Develop, update, and optimize internal compliance policies and procedures to reflect current regulations.
3. Prepare and submit compliance reports, maintaining effective communication with regulatory authorities.

• Team Collaboration:

1. Work closely with technical teams, including Firmware Engineers and Integration Engineers, to validate the compliance of products and systems.
2. Provide compliance guidance and training to other teams to promote a culture of regulatory awareness.

• Risk Identification and Management:

1. Identify potential compliance risks and recommend actionable improvements to mitigate them.
2. Lead quality and compliance enhancement projects, ensuring continuous improvement in these areas.

Requirements

• A bachelor’s degree in Engineering, Quality Management, Law, or a related field, with at least 3 years of experience in product quality or compliance management. Equivalent professional experience will also be considered.
• Strong understanding of regulatory requirements for EV charging systems or IoT products, including certifications such as TR25.
• Experience managing audits and certification processes with regulatory bodies.
• Proven ability to collaborate effectively with cross-functional teams to ensure adherence to compliance and quality standards.
• Strong analytical and problem-solving skills with meticulous attention to detail in documentation and reporting.
• Knowledge of operational compliance standards, such as data privacy laws or environmental regulations, is a plus.

Reporting to:

Project Manager

Responsibilities:

• Online Quality Checking (Metal Detector, Cooker, Pasteurizer, Steamer)
• Online Finished Product Testing
• Monthly Verification of CCP (Critical Control Point)
• Online Verification Sampling for Microbial Analysis
• Internal Calibration of Weighing Scales
• Verification on goods return
• Handle Customers’ Complaint
• Conduct routine physical, chemical, sensory and other analyses accordingly.
• Take appropriate decisions for rework of material based on historical trend and in consultation with seniors
• Raise non-conformation for quality deviations of Raw Material/Finished Goods and follow up with proper closure of corrective and preventive action
• Initiate actions to investigate customer complaint in consultation with relevant team members
• Collect comprehensive evidence/crucial data, provide sound reasoning and propose possible root cause for customer complaints and internal rejection
• Maintain up-to-date quality control programs, policies, process workflows, procedures and work instructions

REQUIREMENTS:

• Diploma / Degree in Food Science preferred
• More than 2 years of relevant experience will be considered for Senior position
• Experienced and passionate in Continuous Improvement
• Exceptional problem-solving skills
• Good Knowledge of Quality Management Systems (HACCP, BRC, ISO 22000)
• Good Communication, Organizational and Analytical Skills
• Strong ability to work well in a team and independently
• Excellent IT skills, particularly in MS Excel, PowerPoint, Word, Access
• Ability to work with multiple priorities in a fast-paced environment is required.
• 5 Days Work Week + 1 Saturday
• Undertake any other ad-hoc projects/ tasks assigned
• Job Scope, Work Day and Work Hours subject to changes depending on work requirement
• Fresh grads are welcome
• Salary package commensurate with experience

• Manage the full spectrum of Quality Assurance and Quality Control activities, including equipment buy‑off (IBO and CBO) requirements and timely closure of internal and external CARS.
• Continuously review and update QA systems, workflows, and documentation; spearhead improvement initiatives to drive performance beyond compliance with standards.
• Drive supplier quality performance through audits, qualification, and re‑certification of vendors, supporting the company’s supply chain development efforts.
• Compile weekly and monthly QA reports, ensuring clear communication of quality performance and improvement actions across teams.

Requirements:

• Diploma in Mechanical, Production, or Mechatronics Engineering.
• At least 3 years of QA experience in a manufacturing environment.
• Proficient in metrology tools and techniques (e.g., Vernier Caliper, Micrometer, Height & Depth Gauge, Profile Projector, Gauge Block, Smart Scope) and problem‑solving methods such as 8D discipline, FMEA, and QC data analysis tools.
• Strong communication skills, detail‑oriented, proactive, and able to drive quality improvement programs independently while working effectively in a team.

If you are keen to apply for the position, kindly email your detailed resume in MS Word to hr@recruit-expert.com

Please note that only shortlisted candidates will be notified.

For more job opportunities, please visit our website at www.recruit-expert.com

EA Licence: 19C9701
Registration: R21100996