Total 21 quality assurance job vacancies in Singapore

Our client is a global leader specializing in high-performance cooling systems, gaming peripherals, and PC components.

Overview:
We are looking for a driven and experienced Quality Manager to oversee quality assurance efforts in the field of thermal solutions for cloud data centers. This role is key to maintaining product excellence through effective quality control systems, fostering continuous improvement, and leading a collaborative team. If you have a strong passion for quality management and thrive in dynamic environments, this opportunity is for you.

The incumbent will be based in Hanoi for more than 6 months per year as part of the company's expansion plans and setting up of a manufacturing facility in Vietnam.

Key Responsibilities:

• Quality Assurance & Yield Optimization:Establish advanced monitoring systems to maintain product quality and optimize yield.
  Identify and execute strategies for improving overall product performance.
• Managing Quality Issues:Address and resolve abnormal quality issues within the manufacturing process.
  Work with cross-functional teams to develop and implement preventive measures.
• Process & Quality Improvement:Enhance internal quality control and improve process capabilities.
  Apply best practices to streamline workflows and maximize efficiency.
• Customer-Focused Quality Management:Lead efforts to resolve customer-reported quality issues, providing detailed corrective action plans.
  Share preventive recommendations with stakeholders to prevent recurrence.
• Inspection & Technological Advancements:Optimize quality inspection processes by integrating automation and advanced tools.
  Drive efficiency improvements in inspection planning.
• Collaborative Communication:Foster effective communication and alignment across departments to support quality objectives.
  Act as a bridge between teams to ensure cohesive quality management strategies.
• Team Leadership & Development:Manage team responsibilities, performance, and task assignments.
  Implement training programs to enhance the team's expertise and skills.
• Project Supervision:Oversee timely delivery of tasks and ensure adherence to quality standards and deadlines.

Qualifications:

• Bachelor's degree and above in a relevant field.
• Proven expertise in quality management, particularly in manufacturing processes.
• Strong analytical and leadership skills with effective problem-solving capabilities.
• Proficiency in quality management systems and standards.
• Excellent communication and team collaboration abilities.
• Certifications in quality management (e.g., Six Sigma) are an advantage.
• Willingness to travel and be based overseas at the manufacturing facilities (~6 months a year)

This role offers an exciting opportunity to lead quality assurance efforts in a fast-evolving sector while driving impactful improvements and fostering innovation.

Interested applicants, please click on "apply" with your updated resume attached.

Our client is a global leader specializing in high-performance cooling systems, gaming peripherals, and PC components.

Role Summary:
We are seeking an experienced Senior Design Quality Engineer to drive quality improvements for thermal cooling solutions. In this role, you will oversee design and process quality, ensuring products meet the highest standards of excellence. This position offers the opportunity to lead cross-functional initiatives and optimize production processes within a dynamic, global environment.

The incumbent will be based in Hanoi, Vietnam as part of the company's expansion plans and setting up of a manufacturing facility in Vietnam.

Key Responsibilities:

• Quality Monitoring & Optimization: Develop and implement advanced systems to monitor and enhance product quality and yield. Lead initiatives to identify and rectify areas for improvement.
• Quality Issue Management: Address and resolve abnormal quality issues in manufacturing processes. Work collaboratively across teams to implement corrective and preventive measures.
• Process Enhancement: Strengthen internal quality controls and enhance process efficiency, driving operational excellence.
• Customer Quality Assurance: Lead investigations into customer-reported issues, ensuring effective corrective actions and preventive solutions are communicated to stakeholders.
• Inspection Process Improvement: Optimize inspection processes, integrating automation and advanced technologies where applicable.
• Cross-Functional Collaboration: Coordinate closely with design, production, and other teams to maintain rigorous quality standards.
• Team Leadership: Oversee the performance, development, and task allocation of the quality team, ensuring timely delivery of objectives.

Qualifications:

• Bachelor’s degree or higher in a relevant field.
• Demonstrated experience in quality engineering, particularly in manufacturing and design quality.
• Strong analytical and problem-solving abilities, with proven leadership skills.
• Knowledge of quality management systems and industry standards.
• Certifications such as Six Sigma are advantageous.
• Willing to be based in Vietnam and travel where required

This role is ideal for a dedicated professional passionate about quality control and process improvement in the electronics industry. If you're ready to take on a leadership position in a fast-paced, innovative environment, we encourage you to apply!

Please click on "apply" with your updated resume attached.

Our client is a global leader specializing in high-performance cooling systems, gaming peripherals, and PC components.

Role Summary:

We are seeking a Senior Supplier Quality Engineer (SQE) to manage and enhance supplier quality for thermal cooling solutions within the electronics and computing sectors. The role involves collaborating with suppliers to ensure compliance with quality standards, improving processes, and resolving quality-related issues. This position is ideal for individuals passionate about quality assurance, process optimization, and supplier development.

The incumbent will be based in Hanoi, Vietnam as part of the company's expansion plans and setting up of a manufacturing facility in Vietnam.

Key Responsibilities:

• Supplier Quality Assurance: Develop and implement monitoring systems to ensure supplier materials and components consistently meet quality requirements. Address and resolve non-conformance issues.
• Process Optimization: Work with suppliers to enhance their production processes, ensuring improved yield and consistent quality in delivered materials.
• Issue Management: Lead investigations into quality issues, implementing effective corrective and preventive actions to mitigate risks.
• Supplier Audits: Conduct audits to assess suppliers' quality systems, process capabilities, and compliance with industry standards. Drive actionable improvements based on findings.
• Supplier Development: Support suppliers in aligning their quality practices with company and customer expectations, fostering long-term collaboration.
• Team Collaboration: Liaise with design, production, and procurement teams to align on supplier quality expectations and enhance communication across functions.
• Continuous Improvement: Advocate for a culture of quality excellence by collaborating with suppliers to refine their quality management systems and manufacturing practices.

Qualifications:

• Bachelor’s degree or higher in a relevant field.
• Extensive experience in supplier quality engineering, ideally within manufacturing or electronics.
• Strong understanding of quality management systems and standards.
• Proficient in supplier audits, corrective action implementation, and continuous improvement methodologies.
• Certifications such as Six Sigma are advantageous.
• Excellent analytical and negotiation skills.
• Willing to travel frequently and be based in Vietnam

This is an exciting opportunity for quality professionals to work closely with suppliers, ensuring the highest standards of quality in an innovative and fast-paced industry.

Interested applicants, please click on "apply" with your updated resume attached.

Quality Lab Support Coordinator

6 months contract

About the Company:
Our client is a US healthcare and a leading global biopharmaceutical company. They have a revenue of US $40.1 billion, with more than 69,000 employees across 140 countries with a heritage of more than 125 years. Our client is committed to provide patients and customers with a reliable supply of high-quality, safe, and effective medicines and vaccines. Their global supply strategy relies on manufacturing capabilities and expertise to achieve this mission

Responsibilities:

In this role, you will be responsible for all or subset of the key responsibilities below:

• Receive, archive, retrieve and dispose retention sample, following standard work, approved procedures and regulatory requirements in timely manner.
• Maintain proper 5S and ensure inspection readiness of retention sample rooms.
• Perform assigned tasks within stipulated timeline and escalate discrepancies to Reporting Manager.
• Support laboratory supplies stock check, receiving, stock arrangement and disposal as necessary.
• Any other duties as assigned by reporting manager.

Requirements:

• GCE O Level qualification and above
• Proficient with computer software such as Microsoft Word & Excel
• The role will require the person to be able to move heavy boxes up to 15 KG during process like transfer of samples/stocks checking.
• Customer focus with strong business acumen and continuous improvement mindset.
• Critical thinking mindset with a collaborative and problem-solving attitude.
• Good communication and interpersonal skills.
• Ability to work effectively in a team-based environment.

Reg No: R22104540

EA License no: 94C3609

Company overview:

Our client is a Global MNC in the mobility technology sector, known for pioneering safer, greener, and more connected solutions for future mobility.

Role Overview:
The successful candidate will support our client in enhancing quality standards and ensuring customer satisfaction throughout product launches.

Responsibilities include:

• Reviewing customer-specific quality requirements and implementing these through Advanced Product Quality Planning (APQP) tools like Process Flow Diagrams and Control Plans.
• Leading Built-in Quality workshops, collaborating with cross-functional teams, and tracking improvements until full resolution.
• Addressing and improving quality issues for new programs, including product operations reviews and quality performance metrics.
• Heading Material Review Board meetings, resolving deviations and non-conforming cases effectively.
• Securing Production Part Approval from the customer and supporting smooth Start of Production (SOP).
• Responding to customer feedback and returns using Six Sigma and 8D problem-solving methods.
• Documenting and leveraging lessons learned for future program improvements.
• Ensuring compliance with Quality Operating Systems during the product launch phase.

Requirements:

• Bachelor’s degree in Electronics, Mechanical, or Computer Engineering, Physics, or Material Science.
• Strong knowledge of APQP processes and standards such as TS16949, PPAP, FMEA, and Quality Plans.
• Excellent interpersonal, leadership, analytical, and communication skills.
• Minimally 3 years of experience in Quality roles, ideally with a focus on product launches.

This role is an excellent opportunity for quality-focused professionals eager to contribute to advancements in global mobility solutions.

Interested candidates are encouraged to apply by submitting their CV.

(EA: 94C3609/R1442042)

Quality Lab Support Coordinator

6 months contract

About the Company:
Our client is a US healthcare and a leading global biopharmaceutical company. They have a revenue of US $40.1 billion, with more than 69,000 employees across 140 countries with a heritage of more than 125 years. Our client is committed to provide patients and customers with a reliable supply of high-quality, safe, and effective medicines and vaccines. Their global supply strategy relies on manufacturing capabilities and expertise to achieve this mission

Responsibilities:

In this role, you will be responsible for all or subset of the key responsibilities below:

• Receive, archive, retrieve and dispose retention sample, following standard work, approved procedures and regulatory requirements in timely manner.
• Maintain proper 5S and ensure inspection readiness of retention sample rooms.
• Perform assigned tasks within stipulated timeline and escalate discrepancies to Reporting Manager.
• Support laboratory supplies stock check, receiving, stock arrangement and disposal as necessary.
• Any other duties as assigned by reporting manager.

Requirements:

• GCE O Level qualification and above
• Proficient with computer software such as Microsoft Word & Excel
• The role will require the person to be able to move heavy boxes up to 15 KG during process like transfer of samples/stocks checking.
• Customer focus with strong business acumen and continuous improvement mindset.
• Critical thinking mindset with a collaborative and problem-solving attitude.
• Good communication and interpersonal skills.
• Ability to work effectively in a team-based environment.

Reg No: R22104540

EA License no: 94C3609

about the company

My client is a specialised manufacturer serving the aviation market

about the job

• Leader of the Quality Department
• Oversee the inspections of aircraft MRO activities
• Develop quality control mannual and adhere to NAA's Part 145 regulation
• Drive the implementation of process control in critical process that will impact product quality
• Initiate activities and programs for continuous improvement on product quality and manufacturing processes
• Oversee Project Management and Maintenance Planning activities
• Conduct monthly Q&S meeting with management team for continuous improvement

skills & experience required

• Master / Degree in Aviation / Aerospace / Mechanical Engineering
• Minimum 10 years of experience in the aviation manufacturing environment
• Lead auditor for quality ISO9001 / ISO 9100
• Extensive Experience in aviation quality management
• Hold a CAAS Aircraft Maintenance Engineering License
• Willing to work around seletr area

If you are interested in the position
Please include your availability, expected salary and reason for leaving current job.
We regret that only shortlisted candidates will be contacted
EA: 94C3609 / Reg: R1325913

About the role

This role is a hybrid between Quality Assurance and Site Reliability Engineering.

Job Duties

• Develop and refine automation frameworks for testing and infrastructure, while also enhancing and improving the codebase.
• Design, develop, and implement thorough test plans, utilizing both automated and manual testing methods to ensure superior software quality and performance.
• Collaborate closely with Software, Firmware, and Hardware teams to achieve smooth deployments, maintain high software standards, and efficiently resolve issues.

Skills and experience required

• At least a Degree in Computer Science or equivalent
• Experience in C# and Python.
• Experience in at least 2 of the following:

- Test Automation Framework (preference for Pytest and Great Expectations)
- CI/CD
- DevOps
- Embedded Systems
- Instruments like Oscilloscope, AWG, VNA


To apply online please use the apply function, alternatively you may contact Chloe Chen at chloe.chen(@)randstad.com.sg. (EA: 94C3609 /R1768253)

About the role

This role is a hybrid between Quality Assurance and Site Reliability Engineering.

Job Duties

• Develop and refine automation frameworks for testing and infrastructure, while also enhancing and improving the codebase.
• Design, develop, and implement thorough test plans, utilizing both automated and manual testing methods to ensure superior software quality and performance.
• Collaborate closely with Software, Firmware, and Hardware teams to achieve smooth deployments, maintain high software standards, and efficiently resolve issues.

Skills and experience required

• At least a Degree in Computer Science or equivalent
• Experience in C# and Python.
• Experience in at least 2 of the following:

- Test Automation Framework (preference for Pytest and Great Expectations)
- CI/CD
- DevOps
- Embedded Systems
- Instruments like Oscilloscope, AWG, VNA


To apply online please use the apply function, alternatively you may contact Chloe Chen at chloe.chen(@)randstad.com.sg. (EA: 94C3609 /R1768253)

Quality Support, Specialist

(12 month contract)

About the Company:

Our client is a US healthcare and a leading global biopharmaceutical company. They have a revenue of US $40.1 billion, with more than 69,000 employees across 140 countries with a heritage of more than 125 years. Our client is committed to provide patients and customers with a reliable supply of high-quality, safe, and effective medicines and vaccines. Their global supply strategy relies on manufacturing capabilities and expertise to achieve this mission

Primary Responsibilities:

The role will ensure and maintain high standards of quality and compliance within client’s organization.

In this role, you will be responsible for all or subset of the key responsibilities below:

• Perform laboratory system lifecycle management, including system qualification/retirement, commissioning/decommissioning, calibration and maintenance, system administration, and periodic reviews, in accordance with approved procedures and standard lead time.
• Raise Computerize Maintenance Management System (CMMS) request form to create/update/delete SAP master data related to laboratory system.
• Raise purchase request and perform orders confirmation and accrual for laboratory system lifecycle management, inventories, maintenance and repairs orders.
• Liaise with vendor to ensure contractor management documentation and assigned vendor tasks are completed within assigned lead time.
• Perform and review of Quality documents such as eshopfloor logs, eVal and etc.
• Assist in conducting laboratory investigations and ensure effective implementation of related actions within the agreed timeframe.
• Provide inputs for the development and revision of Standard Operating Procedures, Work Instructions and other GMP documents.
• Maintain proper laboratory/storage area housekeeping/5S and ensure inspection readiness.
• Execute section and Quality improvement initiatives and other special projects.
• Any other duties as assigned by reporting manager
• Provide skills training to other team members, ensuring they have the necessary knowledge and competencies to perform their duties effectively.
• Conduct troubleshooting of laboratory system lifecycle, identifying and resolving any issues that may impact the business/work efficiency.
• Assume role of Subject-Matter-Expert of laboratory system lifecycle, collaborates closely with other site and above-site functions. This includes actively participating in discussions, sharing expertise, and providing input to ensure alignment and consistency across the organization.
• Support Reporting Manager in planning of routine operations tasks to ensure completion within stipulated timeline.
• Support and respond to audit requirements and findings.
• Perform assessments of compendial updates and implement changes to Standard Operating Procedures, Work Instructions and other GMP documents.

Requirements:

• Diploma or Bachelor’s degree in Science/ Life Science, Pharmaceutical Science or Engineering or any other relevant field
• At least 3 years of relevant working experience in GMP environment with quality control laboratory experience within the pharmaceutical/chemical manufacturing.
• Competency in analytical chemistry tools such as HPLC, root cause analysis methods and tools.

Reg No: R22104540

EA License no: 94C3609

Quality Support, Associate Specialist

(12 month contract)

About the Company:

Our client is a US healthcare and a leading global biopharmaceutical company. They have a revenue of US $40.1 billion, with more than 69,000 employees across 140 countries with a heritage of more than 125 years. Our client is committed to provide patients and customers with a reliable supply of high-quality, safe, and effective medicines and vaccines. Their global supply strategy relies on manufacturing capabilities and expertise to achieve this mission

Primary Responsibilities:

The role will ensure and maintain high standards of quality and compliance within client’s organization.

In this role, you will be responsible for all or subset of the key responsibilities below:

• Perform laboratory system lifecycle management, including system qualification/retirement, commissioning/decommissioning, calibration and maintenance, system administration, and periodic reviews, in accordance with approved procedures and standard lead time.
• Raise Computerize Maintenance Management System (CMMS) request form to create/update/delete SAP master data related to laboratory system.
• Raise purchase request and perform orders confirmation and accrual for laboratory system lifecycle management, inventories, maintenance and repairs orders.
• Liaise with vendor to ensure contractor management documentation and assigned vendor tasks are completed within assigned lead time.
• Perform and review of Quality documents such as eshopfloor logs, eVal and etc.
• Assist in conducting laboratory investigations and ensure effective implementation of related actions within the agreed timeframe.
• Provide inputs for the development and revision of Standard Operating Procedures, Work Instructions and other GMP documents.
• Maintain proper laboratory/storage area housekeeping/5S and ensure inspection readiness.
• Execute section and Quality improvement initiatives and other special projects.
• Any other duties as assigned by reporting manager
• Provide skills training to other team members, ensuring they have the necessary knowledge and competencies to perform their duties effectively.
• Conduct troubleshooting of laboratory system lifecycle, identifying and resolving any issues that may impact the business/work efficiency.
• Assume role of Subject-Matter-Expert of laboratory system lifecycle, collaborates closely with other site and above-site functions. This includes actively participating in discussions, sharing expertise, and providing input to ensure alignment and consistency across the organization.
• Support Reporting Manager in planning of routine operations tasks to ensure completion within stipulated timeline.
• Support and respond to audit requirements and findings.
• Perform assessments of compendial updates and implement changes to Standard Operating Procedures, Work Instructions and other GMP documents.

Requirements:

• Diploma or Bachelor’s degree in Science/ Life Science, Pharmaceutical Science or Engineering or any other relevant field
• At least 1 year of relevant working experience in GMP environment with quality control laboratory experience within the pharmaceutical/chemical manufacturing.
• Competency in analytical chemistry tools such as HPLC, root cause analysis methods and tools.

Reg No: R22104540

EA License no: 94C3609

about the company

Our client designs, manufactures equipment and materials in the chemical industry. They have the people and ethos to act with speed, innovation, enterprise and creativity. The scope of the offer, the size of the business, the autonomoy to drive your career forward all adds up to a great place to work.

about the job

• Conducting internal system audit/ process audit
• Support and troubleshoot necessary QC equipment such as HPLC, DSC, UV spectrophotometer
• Continuous improvement using Lean and Six Sigma tools
• Ensure necessary QC support for the NPI and NPT process
• Perform/ monitor stability program for new products and transfer products

skills & experience required

• Degree/Diploma / Higher NITEC / NITEC in material science / chemical engineering or equivalent
• Min 3 years in medical / chemical / pharma manufacturing environment
• Able to commence within a short notice / immediately will be a plus
• Auditor in ISO 9001/ ISO13485/ IATF 16949 will be a plus

If you are interested in the position

Please include your availability, expected salary and reason for leaving current job.

We regret that only shortlisted candidates will be contacted

EA: 94C3609 / Reg: R1325913

Quality Specialist

(12-month contract)

About the Company:

Our client is a US healthcare and a leading global biopharmaceutical company. They have a revenue of US $40.1 billion, with more than 69,000 employees across 140 countries with a heritage of more than 125 years. Our client is committed to provide patients and customers with a reliable supply of high-quality, safe, and effective medicines and vaccines. Their global supply strategy relies on manufacturing capabilities and expertise to achieve this mission

Primary Responsibilities:

The incumbent will provide quality oversight on manufacturing site operations at the shop floor and co-ordinates with central quality functions as needed. The role will ensure and maintain high standards of quality and compliance within our organization.

In this role, you will be responsible for all or subset of the key responsibilities below:

• Act as a primary quality contact for assigned IPT & provide day-to-day quality support/guidance to IPT operations including quality decisions for manufacturing related events on the shopfloor.
• Represent quality at Integrated Process Team (IPT) tier meetings (example- Tier-2, Tier-4, Micro Tier), liaise with other quality functions for cascades or escalations to & from IPT Tiers.
• Review & assess events reported on the shopfloor, concur justifications to continue the operations or instruct to stop the operations while pending formal initial quality assessment.
• Participate shopfloor GEMBAs to ensure permanent inspection readiness of the site. Support audit & inspection resource room as assigned by the Manager.
• Act as a quality representative for assigned New Product Introduction (NPI) project & provide quality oversight on manufacturing of developmental batches, clinical manufacturing, process/packaging performance qualifications, equipment qualifications, certificate of analysis profile set-up, material creations, equipment & process change controls, and ensure pre-PAI readiness etc.
• Quality review & approval of documents related to development & qualification of process & cleaning, examples include but limited to - protocol & report for cleaning development cleaning validation, process development, process performance qualification, Initial Continued process verification (CPV), campaign length extensions, dirty/clean hold time changes etc.
• Quality oversight on new/revised electronic or paper documents to support routine production operations, examples include but not limited to –Production batch sheets, cleaning batch sheets, re-packaging protocols, Bill of Materials (BOM) memo, Engineering Record (ER) in IPI, Engineering Change Order (ECO) in SAP, Manufacturing Execution System (MES), non-routine Batch Sheet (BS), e-Log for Batch Sheet (BS) redline markups etc.
• Review & Approval of Statistical Process Control (SPC) limit report, Yield reports
• Perform quality review & approval of routine production/facilities related documents including but not limited to – Environment Management System (EMS) review for manufacturing, warehouse and labs, pest control review, preventive & correction maintenance (PM&CM) extension requests.
• Review non-routine/risk release of equipment/utilities/room, batch risk processing requests & support related material control actions.
• Support ad hoc requests for samples, joint inspections of rejected materials/damaged incoming goods, Time-Out-of-Cold-Storage (TOCS) adjustments in SAP, shelf-life extension requests etc.
• Perform any other tasks as assigned by Manager
• Provide quality oversight for the Aseptic Process Simulation (APS) and Aseptic Observer Program (AOP) such as quality monitoring, review and approval of APS protocol and report
• Review and approve performance qualification protocol, equipment & utilities re-qualification protocols or EM re-qualification protocols.
• Review/Approval of Re-packaging protocol for pre-execution
• Review and approve relevant Artwork.

Requirements:

• Diploma or bachelor’s degree in science/ Life Science, Pharmaceutical Science or Engineering or any other relevant field
• Minimum 5 years of applied professional work experience in quality control/assurance in pharmaceutical manufacturing environment.
• Competency in root cause analysis methods and tools.
• Experience in new product introduction or technology transfers.

Reg No: R22104540

EA License no: 94C3609

about the company
Our client is a renowned insurance firm in Singapore. They are now looking for a Compliance Assurance Analyst (AML) to be responsible for supporting customer on-boarding operations and Anti-Money Laundering functions.

about the job

• You will be responsible for conducting thorough reviews, assessments, and audits to assess compliance levels and identify areas for improvement.
• Perform comprehensive reviews of business operations, processes, and procedures to ensure compliance with applicable laws, regulations, and internal policies.
• Assist in name screening and Anti-Money Laundering support.

about the manager/team
This role lies within the Operations team.

skills and experience required

• Minimum Bachelor's degree in Business Administration, Finance, Law, or related field.
• Proven experience in compliance or operations roles within the financial services industry, especially in the banking or insurance sector.

about the company

Our client is a leading system integrator in the construction & project management. They’re now on a look out for a Quality Engineer/Manager to join their dynamic team.

about the job

• Implement, maintain and improve the quality management system (QMS)
• Drive quality improvements and proactive participation in continuous improvement and process improvement projects
• Interact with clients & Accreditation Bodies and be responsible for advising operational colleagues of the importance of quality, accuracy and integrity in the provision of the testing, calibration inspection and certification services we provide.
• Ensure buy-in to the effective implementation of our quality policies and procedure
• Manage scheduled internal audits across management system and technical disciplines
• Manage external and internal proficiency testing programs and prepare compliance and improvement metrics as required.
• Write and review quality documentation and effective and efficient management of personal work schedules and timely generation of quality reports.

job requirement

• Degree / Diploma in Engineering
• Minimum 4 years of managing quality management systems
• Project management experience
• Certified Lead Auditor in ISO9001,ISO14001,ISO45001 would be a huge plus
• Construction / MRT project experience will be a plus
• Able to commence immediately or within short notice period

If you are interested in the position , kindly send your CVs in to yitwei.kwan(@)randstad.com.sg

Please include your availability, expected salary and reason for leaving current job

We regret that only shortlisted candidates will be contacted

EA: 94C3609 / Reg: R1325913

About the company

Our client is a leading provider of analytical and scientific instruments, offering innovative solutions and they are looking for a highly motivated Quality Specialist to join the team.

About the job

As a Quality Specialist for the organization, you are required to:

• Conduct quality control checks and tests on analytical instruments and equipment to ensure compliance with specifications and standards.
• Develop and implement quality assurance and quality control procedures and protocols for analytical testing processes.
• Analyze and interpret data from analytical tests to identify trends, patterns, and deviations.
• Investigate and troubleshoot quality issues, deviations, and non-conformances to determine root causes and implement corrective actions.
• Collaborate with cross-functional teams including R&D, manufacturing, and quality assurance to address quality-related issues.

Requirements

• To succeed in this role, you must possess a Degree in related disciplines, preferably with minimum 2 years of related work experience
• Having strong analytical skills and the ability to remain patient in challenging situations are essential qualities.
• Demonstrating a persistent drive to solve complex technical problems will be highly beneficial.
• Strong communication and interpersonal skills

To apply online please use the 'apply' function

(EA: 94C3609/R22107967)

Applicants must be fully vaccinated or have a valid exemption in accordance with MOM’s regulations to allow them to enter the workplace. Applicants may be required to share verifiable COVID-19 vaccination documents or proof of a valid exemption at the point of offer. Randstad Pte. Limited and/or the Client reserves the right to withdraw an offer if the applicant fails to provide verifiable COVID-19 vaccination and/or proof of exemption documents

about the company:

Our client specializes in offering engineering design and consultancy services to facilitate oil and gas extraction and offshore exploration endeavors.

• Salary Range: up to $12,000/month + Completion Bonus
• Duration: 24 months contract

Job summary:

Lead a team of Supplier Inspection Coordinators to ensure the quality of procured equipment aligns with PO requirements. Establishing project-specific processes and serving as a central contact for client, Project Procurement Manager, and Project Quality Manager on supplier quality matters.

Responsibilities:

• Facilitate effective communication with clients, suppliers, and stakeholders on inspection matters to ensure project quality compliance.
• Manage the Supplier Inspection Management Plan (SIMP) for streamlined inspection coordination.
• Oversee the timely handling of Notice of Inspections (NOIs) and inspection reports from Third-party inspectors (TPIs) through package Supplier Inspection Coordinators (SICs).
• Review supplier bids and contribute to technical bid evaluations.
• Provide input to Inspection & Test Plans (ITPs) and other supplier-related Quality Assurance/Quality Control (QA/QC) documents to support SICs in document review.
• Resolve inspection process issues by collaborating with SICs, Package Managers, Package Engineers, and the Procurement team.
• Identify and mitigate potential risks in the supplier inspection process with Supplier Quality Management (SQM).
• Develop and manage inspection budget plans and forecasts.
• Monitor Notification of Inspection (NOI) tracker, IRC register, Ex inspection register, etc., for accurate Key Performance Indicators (KPI) data reporting.
• Ensure readiness for Factory Acceptance Tests (FAT), Pre-Release Readiness Reviews, and Inspection Release Certificate (IRC) issuance.
• Plan and execute Ex-inspections and other Inspection Test Records (ITR) inspections according to project expectations.
• Timely identification, issuance, tracking, and closeout of supplier Non-Conformance Reports (NCRs).

Requirements:

• Degree/Diploma in Mechanical or a relevant Engineering discipline.
• Minimum of 7 years of experience in onshore/offshore Oil & Gas or FPSO operations.
• Mandatory certifications: CSWIP/AWS, ISO 9001:2015 Lead Quality Auditor.
• Familiarity with international material standards, pressure/process piping and vessel codes, building structural and electrical codes, NDT, welding procedures, and ASME/ANSI codes.
• Proficient in Welding Inspection/Non-Destructive Testing methods.
• Working knowledge of quality assurance, quality control, Classification, and Certification processes.

If you are interested in the position , kindly send your CVs in to gracelyn.teo(@)randstad.com.sg or +65 98254517

We regret that only shortlisted candidates will be contacted

(EA: 94C3609/ R21101213 )

about the company

Our client is a leading materials testing laboratories and solutions provider for a wide range of fields including construction, life sciences, environmental, energy, transportation etc. They’re now on a look out for a Quality Engineer/Manager to join their dynamic team.

about the job

• Implement, maintain and improve the quality management system (QMS)
• Drive quality improvements and proactive participation in continuous improvement and process improvement projects
• Represent our Singapore and Malaysia business units during assessments by accreditation bodies and audits by clients and controlled document holding
• Interact with clients & Accreditation Bodies and be responsible for advising operational colleagues of the importance of quality, accuracy and integrity in the provision of the testing, calibration inspection and certification services we provide.
• Ensure buy-in to the effective implementation of our quality policies and procedure
• Manage scheduled internal audits across management system and technical disciplines
• Monitor laboratory test equipment for calibration currency and advise management of upcoming schedules,ensuring corrective and preventive actions identified within specific laboratories are implemented and verified in a timely manner.
• Manage external and internal proficiency testing programs and prepare compliance and improvement metrics as required.
• Write and review quality documentation and effective and efficient management of personal work schedules and timely generation of quality reports.

job requirement

• Diploma/Degree of Science or Engineering qualification.
• Minimum 2 years of managing quality management systems within a multi-discipline testing, inspection and certification environment
• Candidates with more experience (min 4 years) can be considered for the Quality Manager position.
• Demonstrable experience auditing against ISO/IEC 17025, ISO/IEC 17020 and ISO/IEC 17065.
• Sound knowledge of equipment calibration and analyzing proficiency test data.

If you are interested in the position, kindly apply directly or send your CVs to yiling.tan@randstad.com.sg.

We regret that only shortlisted candidates will be contacted

EA: 94C3609 / Reg: R21103172

about the company

Our client is a biotech company reputable for their immunotherapies with the aim to meet the needs in cancer treatment. With a world-leading combination of technology transfer and their in-house R&D, they are well positioned with global talents in the industry. They’re now looking for a QC Executive to join their team during this exciting time.

about the job

• Perform QC for incoming material, in-process and finished products.
• Conduct performance qualification for equipment and method validation for QC assays.
• Perform QC stability tests (in-use, long-term, shipment, etc) according to GMP and regulatory requirements.
• Troubleshoot on product and quality issues before, during and after production.
• Maintain and clean lab equipment routinely (flow cytometer, PCR thermal cycler, etc.).
• Act as QC document controller through liaison with QA document control
• Be responsible for coordination of QC sample shipment and testing with external testing laboratories
• To support the manager in reviewing protocols/reports/SOPs and other documents assigned by the manager.
• Escalate quality and compliance risks to QC Management and QA.

job requirement

• Diploma/Degree in Engineering (Chemical/Biomedical), Biotechnology, Life Sciences or equivalent.
• Minimum 2-3 years of relevant working experience.
• GMP experience is a plus.
• Experienced in performing routine quality control checks
• Working knowledge in regulatory requirements pertaining to the relevant technical role.

If you are interested in the position, kindly apply directly or send your CVs to yiling.tan@randstad.com.sg.

We regret that only shortlisted candidates will be contacted.

EA: 94C3609 / Reg: R21103172

about the company

Our client is a biotech company reputable for their immunotherapies with the aim to meet the needs in cancer treatment. With a world-leading combination of technology transfer and their in-house R&D, they are well positioned with global talents in the industry. They’re now looking for a dedicated QC Manager to join their team during this exciting time.

about the job

• Perform quality control tests for clinical materials (cell therapy products) according to GMP standards.
• Work with the Cell Manufacturing & Quality Assurance Team.
• Ensuring GMP compliance is maintained at all times.
• Be accountable for the highest level of execution of regulatory strategies, and standards of quality compliance.

job requirement

• Degree in cell biology/biomedical sciences or in a similar medical technology related field.
• Possess experience in quality control tests of biologics or immune cell products
• Experience in regulatory filing with FDA/HSA is desired.
• Familiar with regular testing methods (i.e. sterility/mycoplasma/endotoxin detection, flow cytometry analysis; Cytokine measurement assays; qPCR assays etc.)

If you are interested in the position, kindly apply directly or send your CVs to yiling.tan@randstad.com.sg.

We regret that only shortlisted candidates will be contacted.

EA: 94C3609 / Reg: R21103172

about the company

Our client is a leading rubber manufacturer. They’re now looking for a Quality Assurance Engineer to join their dynamic team during an exciting time in their development.

about the job

• Perform inspection for in-process and outgoing sub-parts and products
• Review with Engineering/ Production and issue non-conforming material report when non-conformance found
• Perform 8D/ CPAR review on customer returns and work with production
• Compile outgoing inspection checklist
• Create QC plan and checklist
• Assist the QA Manager on internal quality activities
• Liaise with internal production on internal process issues
• Provide findings and process improvement

job requirement

• Degree / Diploma in Mechanical / Electrical & Electronics / Quality / Chemical Engineering /Business Management
• Minimum 3 years of experience in quality management/manufacturing environment
• Able to travel to overseas for work assignment (about 30%-40%)
• Willing to be hands on to go to supplier site for audit etc (rubber plantation)

If you are interested in the position , kindly send your CVs in to yitwei.kwan(@)randstad.com.sg

Please include your availability, expected salary and reason for leaving current job

We regret that only shortlisted candidates will be contacted

EA: 94C3609 / Reg: R1325913