Total 918 Quality Assurance / Control job vacancies

• Well Established Company

• Aerospace Industry

• Salary: $3000 to $5000 + Variable Bonus

• Working location: Seletar

• Working hours: Mon-Fri, 8.30am - 6pm

Job Responsibilities:

• Oversee QA standards and monitoring processes for MRO activities

• Drive continuous improvement and identify maintenance/workshop issues

• Support and maintain Safety Management System (SMS) implementation

• Facilitate hazard identification and risk management

• Track and ensure completion of risk mitigation actions

• Report on company safety performance and recommend training

• Support regulatory and third-party audits

• Conduct supplier evaluation and assessment

• Manage non-conformance processes (internal & external)

• Oversee staff training, approvals, and competency needs

• Lead process improvements and business excellence initiatives

• Maintain audit records and track corrective actions

• Perform root cause and corrective action (RCCA) analysis

• Develop and review MRO procedures

• Monitor equipment calibration and reports

• Assist QA Manager in all QA/QC activities
  

Requirements:

• Degree/Diploma in Mechanical, Manufacturing, or Production Engineering.

• 3 years of experience in Aerospace Quality and Auditing, with a minimum of 3 years as a QMS Auditor or Lead Auditor.

• Familiar with AS9100 and EASA/FAA/CAAS/CAAC Part 145.

• NADCAP Special Process Auditing experience (e.g. Non-Destructive Testing, Chemical Processing, Welding) is advantageous.​

• CAAS Air Legislation Paper
  

Candidates are encouraged to apply this position via Apply Now button with the following information in the resume

• Work experience and job responsibilities

• Current and expected salary

• Reason for leaving

• Date of availability

• Education background

We regret that only shortlisted candidates will be contacted.

Barry Ang Ze Xin (Reg No : R26159529)

EA Recruitment Pte Ltd

EA License No: 21C0492

Job Description:

• In Charge of auditing and assessing the suitability of suppliers
• Responsible for initiating and managing project transfer
• Responsible for guiding and implementing improvement programs as well as negotiating and balancing capacity among suppliers
• Responsible for FA Inspection of casting and machining services
• In Charge of managing the foundries which include quality and delivery performance
• In charge of handling the non-conformance parts follow up
• Responsible for checking and monitoring suppliers to ensure delivery

Requirements:

• Min Diploma in Mechanical / Precision Engineering or relevant
• Min 5 years of experience in Oil & Gas industry with experience in Supplier Quality
• Oversea travelling is required

To submit your application, please apply online to apply@rn-care.com or call +(65) 6513 5697 for private and confidential discussion.

Your interest will be treated with the strictest of confidence. We regret that only shortlisted candidates will be notified or contacted.

RN Care Pte. Ltd
EA License No: 17C8900

To carry out contract tendering and contract administration work.

Source for suppliers and prepare costing.

Ensure progress of work is within budget and timelines as well as quality and safety objectives.

Assist project engineer in managing contract variation and preparing of project claim.

Manage and oversee the day-to-day construction activities of the project

Assist in design and drawing proposal if require.

To take direct instruction from the management to carry out others duties related to the business of the company.

Role Overview

We are partnering with our client to hire an experienced Quality Engineer to ensure system quality, reliability, and performance across the software development lifecycle.

This role focuses on end-to-end testing, automation, and platform stability, supporting both legacy systems and modern cloud-based applications as part of an ongoing transformation journey.

Employment Type: 1-Year Contract

Key Responsibilities

• Design and execute comprehensive test strategies across the software development lifecycle
• Develop, maintain, and execute both automated and manual test cases
• Perform functional, regression, and exploratory testing
• Manage defects, test artefacts, and quality reporting
• Support system integration testing (SIT) and user acceptance testing (UAT)
• Collaborate with developers and stakeholders to define clear acceptance criteria
• Ensure adequate test coverage, traceability, and quality standards
• Build, enhance, and maintain automated testing frameworks
• Integrate testing into CI/CD pipelines to enable continuous quality assurance
• Monitor application performance, reliability, and system stability
• Support basic environment setup, maintenance, and troubleshooting
• Contribute to improving testing methodologies and team processes
• Maintain clear and structured documentation for test plans and results

Technology Landscape

You will be working within a transformation environment:

• Current Environment: Sybase databases, Java-based applications
• Target Environment: Microsoft Azure (GCC), Azure SQL, .NET-based applications

This role offers exposure to modern QA practices within cloud transformation projects.

Required Skills & Experience

• Minimum 7 years of experience in software testing or quality engineering
• Strong hands-on experience in both manual and automated testing
• Familiarity with test automation tools and frameworks
• Understanding of CI/CD pipelines and modern development practices
• Basic knowledge of cloud platforms (preferably Microsoft Azure)
• Experience with performance and security testing
• Exposure to infrastructure, platform operations, or environment management
• Familiarity with containerisation and Infrastructure-as-Code (IaC) tools is an advantage
• Strong analytical thinking and problem-solving skills
• Good communication and collaboration abilities

All information will be kept strictly confidential. Only shortlisted candidates will be contacted.

TALENT PULSE PTE. LTD.
EA License No: 25S2956

• Basic $4000 to $6000 + Variable Bonus + Allowances
• Excellent Welfare and Benefits + Career progression
• Working location: West / Northeast (Both location available)
• Working hours: 8:30am – 5:30pm (Mon – Fri)
• Automation, Control, PLC Systemw

Job Responsibilities:

• Manage and implement automation projects from start to finish
• Develop software programs for control systems
• Conduct system maintenance, troubleshooting, and user training
• Work in diverse environments including process plant, vessels, and construction sites
• collaborate with cross functional teams to ensure successful project delivery

Requirements:

• Possess Diploma or Bachelor's Degree in Electrical & Electronic Engineering, Mechatronics, or related field
• Familiar with industrial automation system and control instrumentation
• 2 to 3 years of relevant working experience in industrial automation or control systems

Candidates are encouraged to apply this position via Apply Now button with the following information in the resume

• Work experiences and job responsibilities
• Current and Expected salary
• Reason for leaving
• Date of availability
• Education background

We regret that only shortlisted candidates will be contacted.

NG DIAUM YEE (R2198031)

EA Recruitment Pte Ltd

EA License No: 21C0492

HAID BIOTECHNOLOGY INDUSTRY (SINGAPORE) PTE. LTD. is seeking a meticulous and experienced Quality Control Inspector to join our new startup team in Singapore. The successful candidate will play a vital role in ensuring our products meet established standards of quality, reliability, and performance by monitoring and auditing all phases of the production process.

品管Quality Control Inspector

一、来料检验职责Incoming Material Inspection

按照检验标准对供应商来料进行外观、细度、性能等检查。

Perform inspections on supplier materials according to established standards, including appearance, fineness, and performance.

对不合格物料进行标识、隔离、记录并及时反馈采购与供应商。

Identify, isolate, and record non-conforming materials, providing timely feedback to Procurement and suppliers.

统计来料不良率，参与供应商质量评估与改善。

Calculate and track the incoming defect rate, and participate in supplier quality evaluation and improvement initiatives.

对检验工具（卡尺、振筛等）进行日常保养与校验状态确认。

Conduct daily maintenance and verify the calibration status of inspection tools (e.g., calipers, vibrating sieves).

二、制程检验职责 In-Process Inspection

按检验计划对生产过程进行首件、巡检、抽检。

Execute first-article, patrol, and sampling inspections based on the inspection plan for the production process.

监督生产按作业指导书、工艺流程执行，发现异常及时制止并上报。

Monitor production to ensure adherence to Work Instructions and process workflows; halt and report any irregularities immediately.

跟踪制程问题的改善过程，确认改善措施的有效性。

Follow up on the correction of process issues and verify the effectiveness of improvement measures.

记录并统计制程不良数据，为工艺优化提供依据。

Record and compile data on in-process defects to provide basis for process optimization.

对关键工序的关键参数进行监控，确保过程稳定。

Monitor key parameters in critical processes to ensure operational stability.

三、成品检验职责Final Product Inspection

按出货标准对成品进行外观、性能等检查。

Inspect finished products for appearance and performance against shipping standards.

对不合格品进行判定、隔离及处理（返工/报废）。

Judge, isolate, and disposition non-conforming products (for rework or scrap).

确保所有出货批次具备完整的检验记录。

Ensure complete inspection records are available for all outgoing batches.

与生产、仓库沟通，避免不良品流入客户。

Liaise with Production and Warehouse to prevent defective products from reaching the customer.

四、质量异常处理 Quality Exception Handling

发现质量异常及时报告并推动异常分析。

Report quality anomalies promptly and drive root cause analysis.

跟进纠正预防措施的落实与验证。

Follow up on the implementation and verification of corrective and preventive actions.

协助组织质量会议，推动跨部门改善。

Assist in organizing quality meetings and driving cross-departmental improvements.

五、质量文件与记录维护 Quality Documentation & Record Maintenance

负责检验记录、检验报告的填写、整理与归档。

Complete, organize, and archive all inspection records and reports.

维护检验标准、作业指导书等质量相关文件。

Maintain quality-related documents such as inspection standards and work instructions.

协助编制和更新检验规范与SOP。

Assist in the compilation and updating of inspection specifications and SOPs.

六、设备与环境管理 Equipment & Environment Management

负责使用的检验设备的日常点检与维护。

Perform daily spot checks and maintenance on assigned inspection equipment.

确保检验区域的 6S 管理符合要求。

Ensure the 6S management standards are met in the inspection area.

协助设备校准与外部计量机构联系。

Assist with equipment calibration and liaise with external metrology agencies.

七、培训与沟通Training & Communication

对新员工进行质量意识、检验标准的培训。

Conduct training on quality awareness and inspection standards for new employees.

与生产、购销等部门沟通质量问题与改善计划。

Communicate quality issues and improvement plans with Production, Purchasing, and Sales departments.

参与客户投诉问题的调查与回复资料准备。

Participate in the investigation of customer complaints and assist in preparing response reports.

Requirements:

· Diploma or higher in Food Science, Biotechnology, Chemistry, Pharmaceutical, or a related field.

· At least 3 years of working experience in a similar role with proven experience.

· Good command of both verbal and written English and Mandarin to liaise with Mandarin-speaking business associates.

· Able to start immediately or with a short notice period preferred.

· Only Singaporeans/PRs may apply.

Job Description

• Industry/ Organization Type: Manufacturing
• Position Title: Control (Software) Design Engineer / PLC Programmer
• Working Location: Pioneer (Close to Joo Koon MRT)
• Working Hours: 5 days (Mon – Fri, 9am – 6.00pm)
• Salary Package: Up to $3,000 + AWS + Performance Bonus
• Duration: Permanent Role

Key Responsibilities

• Project Management including scheduling, Budget control & other project related matters
• Responsible for hardware and software (PLC) design for customized machine / total system
• To supervise, test and commission projects both in Singapore and/or to overseas
• Project presentation & documentation
• To work with third party engagement wherever necessary for project related matters

APPLY NOW!!!

• Diploma / Degree
• Experience in project management, especially with PLC design and implementation, is preferred.
• Good organizational and communication abilities to handle diverse project aspects.
• Willingness to travel for project supervision and commissioning.

Kindly apply through ANY of the following methods:

• Submit your application by clicking the APPLY button;
• Email your resume to Job@anradus.com.sg. Please indicate #70912 on the email subject.

Anradus Application Policy: We value each application and ensure every resume is reviewed. Our process is efficient, typically concluding within 3 working days. If you do not receive communication from us within this timeframe, it's likely that your application has not been shortlisted by our client. In such cases, we recommend continuing your job search to maximize your opportunities.

Anradus Pte Ltd | EA License No. 20C0161 | Angel Lim | EA Reg No.: R1769781

Location: Singapore (remote + on-site as required)
Engagement: Project-based / Part-time

About Us

AV Intelligence is an engineering-led audio visual and lighting integration firm operating across Singapore and Malaysia.

We focus on premium residential and commercial environments, where system reliability, user experience, and clean integration matter more than brand names.

Role Overview

We are looking for an experienced AV control system programmer to support ongoing and upcoming projects.

This is a project-based role, working alongside our internal team to deliver stable, intuitive, and well-structured control systems across:

• Private home cinemas and multi-room residences

• Executive offices and boardrooms

• Retail / hospitality environments

Scope of Work

You will be responsible for:

• Programming and commissioning:

  • Savant

  • RTI

  • Lutron (integration level)

• Building clean, intuitive UI/UX (not template-level work)

• System logic structuring (scenes, automation flows, fail-safes)

• Remote testing + on-site commissioning (when required)

• Supporting troubleshooting during final delivery phase

What We Care About (VERY IMPORTANT)

We are not looking for someone who:

• Only follows templates

• Requires step-by-step instructions

• Has only done basic training / certification

We are looking for someone who:

• Has actually deployed systems end-to-end

• Understands real-world integration issues

• Can design logical, user-friendly control flows

• Takes ownership of system stability — not just “getting it to work”

Minimum Requirements

• Proven experience in Savant OR RTI programming (both preferred)

• Familiarity with Lutron integration (RA2 / HomeWorks / QSX)

• Able to demonstrate completed projects (photos / videos / UI screenshots)

• Strong understanding of:

  • AV signal flow

  • Network basics

  • Device communication (IP / IR / RS232)

• Based in Singapore OR able to support Singapore projects

How We Evaluate You (Important)

You will be asked to provide:

1. 2–3 real project examples

   • UI screenshots

   • System description (what you programmed)

2. A short explanation of:

   • How you structure a multi-room AV control system

3. (Optional but strong advantage)

   • A quick walkthrough video of your interface

Engagement Structure

Remuneration posted is monthly for easy reference but the fee will be fixed per project (not hourly tracking)

Compensation is structured per project rather than fixed monthly salary.

Typical range:

• Small systems: SGD 800 – 1,500

• Mid systems: SGD 1,500 – 3,000

• Complex systems: SGD 3,000+

• Remote work + scheduled site visits for commissioning

Why This Role

• Work on high-end, well-designed projects

• Clear scope and structured collaboration

• Long-term pipeline if performance is strong

• Opportunity to grow into lead programming partner

How to Apply

Send the following:

• Brief introduction

• Relevant experience (not generic CV)

• Project examples (required)

• Availability

Job Summary:
The role is responsible for managing compliance controls, financial planning, people administration, procurement, and premises management to ensure smooth operations and adherence to organizational standards.

Key Responsibilities

Controls & Compliance

• Perform control testing, document results, and update outcomes in GRC.

• Conduct independent reviews of Line Managers’ Excessive Access reports and maintain audit evidence.

• Escalate delayed reviews to Division Head to prevent unauthorized system access.

Financial Management

• Prepare annual budgets and year-end accrual plans for operating expenses.

• Develop monthly budget reports and update forecasts.

• Perform headcount reconciliation and monitor Staff Engagement Fund, training, travel, and transport expenses.

• Review monthly forecasts and process AP invoices, including submission of parked vendor invoices and ensuring online approvals.

People Administration

• Manage onboarding: arrange computer setup, apply office access, and update distribution lists.

• Handle offboarding and transfers: ensure return of assets, terminate access, and removal of roles

• Organize monthly People meetings, document minutes, and follow up on actions.

• Maintain accurate organization charts and resolve administrative concerns promptly.

Procurement & Expense Tracking

• Create purchase requisitions for office supplies, PCs, accessories, and services.

• Perform goods receipt for delivered items and services.

• Submit parked vendor invoices and ensure timely approvals.

• Track departmental expenses.

Fixed Assets & Inventory

• Maintain and update fixed assets listing; ensure proper recording and tracking.

• Write off obsolete assets and participate in annual verification exercises.

Manage inventory levels for office supplies and maintain archival records.

• Coordinate Annual Recertification Exercises and maintain Business Role Matrix

Business Continuity & Risk

• Act as Business Continuity Management (BCM) Champion: assist in business impact analysis and Business Continuity Process (BCP) completion, conduct BCM awareness training, and coordinate call tree exercises.

Premises Management

• Serve as BU admin and primary contact for premises-related information and maintenance.

• Collaborate with Service Ambassadors for proper upkeep of office facilities.

• Monitor user access reports to ensure only authorized individuals have office access.

Job requirement:

• Good interpersonal, written, and communication skills with attention to detail.

• Ability to multi-task and manage work tasks with numerous stakeholders, as well as deliver results within tight timelines

• Proficiency in Microsoft Office Suite applications, particularly Excel, Word and Outlook

• Able to work from office full-time

• Relevant working experience with admin roles will be preferred.

We are seeking a Quality Technician to support our expanding manufacturing site in Singapore. This role is responsible for incoming quality and sampling inspections for critical assemblies, ensuring compliance with quality standards and specifications.

Key responsibilities:

• Perform visual, dimensional, and functional inspections on optical components, mechanical fabricated parts, and cables.
• Conduct First Article Inspection (FAI) for optics and related assemblies.
• Follow established sampling plans, inspection procedures and quality standards.
• Maintain accurate and complete inspection records, logs and reports.
• Assist engineers in the investigation of failures and defects in parts and components.
• Identify quality issues and recommend improvements to enhance inspection effectiveness.
• Support First Pass Yield improvement initiatives and assist in identifying root causes for manufacturing low Yield / quality issues.
• Apply continuous improvement concepts and techniques in daily work activities.
• Performs other duties as assigned by supervisor based on business needs.

Requirements:

• Minimum of three (3) years of experience in Quality inspection, Quality tech or related roles.
• ITE / Diploma or higher in engineering or equivalent.
• Able to read and interpret technical drawings, specifications and manufacturing documents.
• Proficiency in using measurement tools (calipers, micrometers, CMM, etc.).
• Familiarity with optics metrology and laser testing will be an advantage.
• Strong attention to detail and good documentation skills.

Job Description:

• In Charge of auditing and assessing the suitability of suppliers
• Responsible for initiating and managing project transfer
• Responsible for guiding and implementing improvement programs as well as negotiating and balancing capacity among suppliers
• Responsible for FA Inspection of casting and machining services
• In Charge of managing the foundries which include quality and delivery performance
• In charge of handling the non-conformance parts follow up
• Responsible for checking and monitoring suppliers to ensure delivery

Requirements:

• Min Diploma in Precision Engineering or relevant
• Min 5 years of experience in Metal Machining industry with experience in QC/ Audit
• Extensive travelling is required

To submit your application, please apply online apply@rn-care.com or call +(65) 6513 5697 for private and confidential discussion.

Your interest will be treated with the strictest of confidence. We regret that only shortlisted candidates will be notified or contacted.

RN Care Pte. Ltd
EA License No: 17C8900

What you'll be doing

• Support risk management activities for medical device and development projects

• Assist in implementing and maintaining Quality Management Systems aligned with ISO 13485, ISO 14971, and IEC 62304

• Prepare and maintain Design History Files and technical documentation

• Collaborate with clinicians and engineering teams to validate requirements and support product de-risking

• Provide day-to-day quality and regulatory support across project lifecycles

• Track project milestones and support coordination across stakeholders

• Contribute to technical reports, grant submissions, and innovation initiatives

• Maintain organised, audit-ready documentation and records

What we're looking for

• Bachelor Degree in Engineering/ Biomedical Engineering/ Science or related studies

• 2 – 4 years of working experience in quality and regulated environments within the medical device industry

• Familiarity with ISO 13485, ISO 14971, IEC 62304, or similar standards

• Strong technical writing, analytical thinking, and communication skills

• Exposure to medical devices, healthcare, or regulated product development is advantageous

• Audit exposure or understanding of software development lifecycle is a plus

Interested applicants, kindly furnish us with your full and detailed resume in MS Words format and click "Apply Now" button.

We regret to inform only shortlisted candidates will be notified. Applicants who do not possess necessary experience or qualification will still be considered on individual merits and may be contacted for other opportunities. 

JobStudio will not solicit any money, request to use your bank account for business or request you to transfer any monies to any parties. Please be aware of scams impersonating JobStudio and our employees. You may call our office directly for verification. We will not be liable for any loss arising from scams.

JOBSTUDIO PTE. LTD.

EA License No: 10C4754

EA Personnel: Ryan Tan En Long

EA Personnel Reg No: R25158265

Our client is one of the world's largest medical technology companies that produce and sell medical equipment, medical systems and reagents, dedicated to improving human health around the world.
For business expansion, our client is hiring one Quality Engineer at their Tuas manufacturing plant.

Quality Engineer (QA/ RCA)
location: Tuas Avenue (Transport provided island-wide)

Plan, co-ordinate and oversee all QA support activities and initiatives in the work cell. To improve process capabilities and product quality to meet the desired targets.

Job Responsibilities:

• Oversee the product quality from assembly to packaging process and ensure full compliance to the Quality System and regulation requirements.
• Champion data-driven decisions to resolve non-conformances, complaint investigation, CAPA, deviation and other quality matters in a timely manner.
• Interfaces with R&D, unit quality, customer quality engineer to formulate plans and actions to meet product specifications and quality requirements.
• Drive quality improvement/automation projects through project planning, scheduling inspection/testing activities, performing analysis and publishing reports.
• Perform test method validation, installation qualification, correlation study for new quality equipment/test method.
• Act as a support role for regulatory, external, internal and/or supplier audits and lead the value stream members to execute the corrective actions for compliance with customer specifications.
• Perform data analysis and trending for product quality performance through monthly and quarterly management review meeting.
• Establish and maintain effective system and procedures to ensure that all manufacturing and engineering documentation are controlled and updated per established regulatory requirements.
• Supervise quality technical specialist and a group of technicians on quality tests and checks.
• Safety & ISO 14001 Environmental accountability: Ensure a safe, healthy and environmentally-friendly workplace by observing Company's rules and procedures.
• Active involvement in prevention, elimination of potential safety hazards and participation in activities which promotes recycling, replacement and reduction of resource materials.
• Perform any other tasks as assigned. 

Job Requirement:

Required:

• Comfortable working at Tuas Avenue, with Company shuttle bus provided island-wide.
• 1-2 years relevant working experiences in a quality engineer role.
• Demonstrated good understanding of key elements of Quality Management system, CFR Part 820, ISO.
• Hands-on experience in Root Cause Analysis.

Preferred:

• Preferably possess Six Sigma Green-Belt certification or knowledge on six sigma tools.
• Able to effectively multi-task and work independently with a high level of initiative
  
  
  What In It For you

Salary: Up to 4200
Location: Chai Chee (moving to Tai Seng in Q4)

Responsibilities:

• Manage incidents, feedback & complaints, ensure timely resolution
• Drive quality improvement, patient safety & risk management initiatives
• Support certifications (e.g. DPTM, Bizsafe) and regulatory compliance
• Review workflows, policies & procedures for quality standards
• Track quality indicators, prepare reports for management
• Maintain documentation control & liaise with MOH/AIC/MOM

Requirements:

• Min. Diploma
• Min. 3 years in healthcare quality / patient safety
• Experience in QA/QI, risk management or data protection
• Knowledge in RCA / FMEA is a plus
• Proficient in MS Office (Excel, PowerPoint)
• Familiar with healthcare regulations

If interested, please email me at alexgoh@recruitexpress.com.sg or telegram @alexgohhl

➖

Alex Goh Hock Leong

(CEI.No: R1763413 l Recruit Express Pte Ltd (Healthcare & Life Science) | 99C4599)

Job Summary
We are seeking a dedicated and certified Pest Control Technician to join our team. The successful candidate will be responsible for implementing vector control measures to prevent and manage vector-borne diseases in various environments.

Key Responsibilities

• Conduct site inspections and carry out vector surveillance.
• Apply appropriate vector control methods including fogging, larviciding, and residual spraying.
• Maintain records of control activities and findings.
• Adhere to safety protocols and standard operating procedures.
• Report any environmental issues or potential vector breeding grounds.
• Coordinate with team members and supervisors to ensure effective execution of control programs.
  
  Requirements
• Candidates with no experience are welcome
• Workplace literacy and numeracy proficiency in reading, listening, and numeracy.
• Preferably with driving license.
• Must be able to work in various outdoor environments.
• Minimum N Level education or equivalent.
  
  

Job Description:

• Contribute to Life Science projects for Antaes Asia clients
• Review and verify executed component batch records for accuracy and compliance with GMP/GDP requirements.
• Perform timely release of raw materials, buffers, and media in SAP in accordance with approved specifications and procedures.
• Support Electronic Batch Record (EBR) review activities for production operations.
• Participate in Quality on the Floor (QOTF), GEMBA walks, and provide real-time guidance to operations personnel on documentation practices and GMP compliance.
• Assist in identifying and escalating documentation or process deviations during record review or shopfloor interactions.
• Collaborate cross-functionally with Production, QC, and Material Management teams to resolve discrepancies or issues related to material release and batch documentation.
• Support QA team in continuous improvement initiatives and data gathering for metrics and trend analysis.
• Contribute to the promotion of Antaes services on top of assistance provided to clients

Job Requirements:

• Diploma in Biomedical Engineering, Biotechnology, Life Science or equivalent
• 1 - 2 years of Quality Assurance/ Manufacturing within a GMP-regulated biologics or pharmaceutical environment.
• Familiarity with Good Manufacturing Practice (GMP) and Good Documentation Practice (GDP).
• Exposure to SAP and Veeva Vault would be preferred
• Candidate must be highly motivated, be able to work independently as well as in a team and have good organizational and oral and written communication skills
• Excellent communication skills, both written and verbal, in English

Position Overview

The IPQC Technician plays a vital role in ensuring product quality during the manufacturing process. By conducting in-process checks and monitoring production activities, this role helps prevent defects and supports compliance with company and industry standards.

Key Responsibilities

• Perform in-process inspections at various stages of production.

• Monitor and record key process parameters to ensure compliance with specifications.

• Identify and report non-conformities promptly to supervisors.

• Assist in root cause analysis and corrective actions for process deviations.

• Ensure proper documentation of inspection results in line with ISO/GMP requirements.

• Collaborate with production and engineering teams to maintain continuous quality improvement.

• Maintain and calibrate inspection tools and equipment.
  

Qualifications

• Diploma/Certificate in Engineering, Manufacturing, or Quality Assurance.

• Fresh graduates or candidates with up to 2 years of experience in quality control are welcome.

• Basic knowledge of manufacturing processes and quality standards (ISO 9001, GMP, etc.).

• Strong attention to detail and ability to follow procedures.

• Good communication and teamwork skills.

Job Description:

• Work as a team to create and implement comprehensive quality assurance plans that outline the processes and procedures for ensuring quality throughout the product lifecycle, from design to manufacturing to delivery.
• Conduct internal and external audits to assess the effectiveness of quality control procedures and identify areas for improvement.
• When quality issues are identified, work to determine the root cause of the problem, develop corrective actions, and monitor their implementation to ensure they are effective.
• Ensure that company's products and services meet relevant industry standards and regulations, including standards like NADCAP.
• Provide training and awareness programs for employees on quality control procedures and best practices.
• Actively participate in continuous improvement projects to enhance quality and reduce costs.
• Collaborate with suppliers to ensure that their products and services meet the required quality standards.

Requirement:

• Min Degree in Engineering
• Min 3 years of experience in certifying staff and lead QA activities

To submit your application, please apply online apply@rn-care.com or call +(65) 6513 5697 for private and confidential discussion.

Your interest will be treated with the strictest of confidence. We regret that only shortlisted candidates will be notified or contacted.

RN Care Pte. Ltd
EA License No: 17C8900

Position Summary

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

Job Scope

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

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

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

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

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

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

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

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

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

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

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

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

Requirements :

1. Hold local pharmacist license

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

3. Experience working in warehouse is desire

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

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

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

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

8. Experience in conducting external and internal audits for regions

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

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

Competency

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

2. Problem-solving skills to support customer issue resolution

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

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

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

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

Working hours:

Mon to Fri 9am-6pm

Key Responsibilities :

• Prepare production campaign start-up, batch review, and review of cleaning records and activities.
• Manage and coordinate Change Control, Event (Deviation and Incident), Out-of-specification (OOS), and resolution.
• Maintain, improve, establish and update appropriate quality management systems to meet customers’ and authorities’ requirements.
• Assist to promote Quality culture for Bulletin, training, and organize promotion activities.
• Assist in quality discussion with respective departments to improve the quality system.
• Assist to plan, prepare and facilitate customers’ and regulatory authorities’ audits and follow-up action.
• Carry out Internal audits of all departments and supplier audits.
• Assist and improve qualification activities and quality risk management.
• Qualification of supplier and external contractor.
• Any other QA department job assigned by the Head of Quality Assurance.

Requirements :

• Degree in Chemical related field or diploma in chemical related field with 3 years relevant experience.
• Proficient with Microsoft Office (Words, Excel)
• Strong oral and written communication in English
• Ability to work as a team in department.
• Good communication and collaboration skills to work with cross-functional teams.
• Working experience in Quality related field is preferred.

PRINCIPAL ACCOUNTABILITIES

Quality Engineer is responsible for making sure that the engineering and manufacturing process are performed correctly using the calibrated and right tools, correct material specs, and processes.

JOB RESPONSIBILITIES

1. Work with Quality Manager to ensure the inspection processes adhere to the relevant work Instructions, quality plan, drawings, and QMS requirement.
2. Leads cross-functional team in customer complaint and internal quality issues investigation and in-charge in driving corrective and preventive actions to prevent recurrence.
3. Analyzes data pertaining to the quality performance and identifies and implements continual improvement.
4. Performs internal audits to ensure the company's compliance with the QMS and customer requirements.
5. Conducts training to improve the competency of the quality inspectors.
6. Arrange with customer’s 3rd party inspector for on-going/pre-delivery of job inspection.
7. Promptly update the progress of on-going job(s) to the customer’s 3rd party inspector.
8. Review and sign-off of a material certificate, certificate of conformance, and testing report.
9. Liaise with supplier/customer on material certificate-related matters.
10. Assist Quality Manager in implementing the Quality Management System.
11. Work with Quality Supervisor/Lead & Quality Manager to monitor process study for improvement in efficiency, manpower saving, and optimal method.
12. Work with Quality Lead in managing the control of drift as per relevant process procedure.
13. Responsible for the accuracy and timely inspection & calibration of monitoring and measuring devices & ensure the use of calibrated and calibrated measuring equipment is practiced for both production (product-related) and quality departments and the Calibrated Measuring Equipment log is maintained.

REQUIRED COMPETENCIES

1. Proven and Solid 3 years of work experience in the same field and in the Oil & Gas Equipment Manufacturing Environment
2. Diploma/Degree in Engineering or related field
3. Knowledge in ISO9001, Quality Management System, Quality Control, and usage of measuring devices/tools.
4. Fluent both in oral and written English.
5. Good team player with a strong commitment to quality, and the ability to work closely and communicate effectively.

*Only shortlisted will be notified.

* Salary is commensurate with qualifications and experience.

Position Overview

We are seeking an experienced Test Engineer with a strong background in software quality assurance and Agile delivery. The successful candidate will be responsible for designing, executing, and improving test strategies across the development lifecycle to ensure the delivery of high‑quality, reliable, and secure software products.

You will work closely with developers, product owners, and business stakeholders to test early, test often, and uphold quality at every stage of the Agile process.

Key Responsibilities

Quality Engineering & Test Design

• Design, develop, and execute test strategies, plans, and test cases to ensure software quality throughout the Agile development lifecycle.
• Design and execute test cases based on acceptance criteria, ensuring new features meet defined quality standards.

Testing & Automation

• Contribute to the automation of test cases and continuous testing processes using relevant tools and frameworks.
• Perform manual and automated testing across functional, integration, system, and UAT stages.

Defect Management

• Identify, document, prioritise, and track defects through resolution.
• Collaborate closely with developers to triage issues, verify fixes, and ensure timely closure.

Agile Collaboration

• Work alongside developers and product owners to test early and frequently within each sprint.
• Ensure quality is maintained consistently throughout the Agile lifecycle.
• Support UAT efforts through preparation of evidence, test artefacts, and functional validation.

Documentation & Reporting

• Ensure test results, logs, and evidence are properly documented and audit‑ready.
• Produce clear, comprehensive, and structured test plans, test cases, and bug reports.

Requirements

• Bachelor’s Degree in Computer Science, Information Systems, Engineering, or a related field.

Extensive professional experience with demonstrated expertise may be considered in lieu of formal qualifications.

• At least 5 years of experience in software quality assurance or testing roles within Agile teams.
• Proficient in manual and automated testing techniques, including unit, integration, system, and UAT testing.
• Experience with test automation frameworks and tools (e.g., Selenium, Cypress, JUnit, TestNG, or similar).
• Familiarity with Agile testing methodologies and continuous testing in CI/CD environments.
• Strong ability to collaborate with developers, business analysts, and users to ensure high‑quality deliverables.
• Highly proficient in writing detailed test plans, test cases, and bug reports with strong attention to detail.

What We Offer

• Opportunity to work on impactful public sector digital platforms.
• Team-first culture with collaborative Agile practices.
• Access to modern testing tools and cloud-based DevOps environments.
• Structured career progression and skills development support.

ABOUT SIOUX
Sioux is a strategic high-tech solutions provider that develops, innovates and assembles complex high-tech systems
We have a team of over 1,200 dedicated engineers who either support our clients or serve as their Research and Development department. Our strong productivity allows us to speed up product development, giving our clients a competitive edge at a better cost-effectiveness.
As a rapidly growing employer, Sioux values its employees' growth and well-being. We invest in their career development and foster a positive work environment that promotes personal and professional growth.

SIOUX IN SINGAPORE

Sioux Singapore plays a pivotal role in the Asian market by offering R&D services from our centers across Europe and Asia to customers, leading development teams in Asia, from Singapore

This expansion allows us to meet the changing needs of our domestic and international (OEM) customers in the semiconductor, analytical, and medical industries.

THE ROLE

As a Motion Control Engineer at Sioux Singapore, you are responsible for the design, development, and optimization of motion control systems for high-precision equipment used in the semiconductor, analytical, and medical industries. You will be part of a multidisciplinary team and work closely with system architects, software engineers, and mechanical designers to deliver reliable and performant motion solutions.

On this career trajectory, you can advance into the role of a lead engineer or system architect in line with the impact and independence of your individual contributions to the team that you are guiding.

Your responsibilities include:

• Designing and implementing motion control algorithms for precision positioning systems (e.g. servo drives, linear motors, piezo stages).
• Translating system-level performance requirements into motion subsystem specifications and control strategies.
• Selecting and integrating motion hardware: servo drives, amplifiers, encoders, and actuators.
• Developing and tuning PID and feed-forward controllers, as well as advanced control strategies such as model-based control and iterative learning control.
• Collaborating with mechanical and electrical engineers to ensure seamless integration of motion systems.
• Performing dynamic modelling and simulation of motion systems using MATLAB/Simulink or equivalent.
• Conducting system-level testing, commissioning, and troubleshooting of motion control systems on-site and at customer locations.
• Conducting peer reviews to ensure product quality.

THE JOB SCOPE

Technically, the job scope comprises the engineering of high-precision motion systems covering the full motion control stack, from low-level drive configuration and real-time control to high-level supervisory and diagnostics software.

In particular, the job scope covers the following:

Real-time motion control implementation using platforms such as Beckhoff TwinCAT, Siemens SIMOTION, or equivalent EtherCAT-based systems. Hardware abstraction and driver integration for servo drives (e.g. Beckhoff, Siemens, Yaskawa), encoders (linear and rotary), and fieldbus interfaces (EtherCAT, PROFINET, CANopen).

Development of device-level and domain-level control logic, including state machines and sequencing for multi-axis coordinated motion.

Implementation of application-layer features such as recipe management, calibration routines, and position error compensation.

Integration and commissioning of motion systems at customer sites.

Creating detailed functional design specifications (FDS), motion system analyses, and test reports.

JOB REQUIREMENTS

Qualifications and Experience

A technical background with a university education in Mechanical Engineering, Electrical Engineering, Mechatronics, Control Engineering, or a related field.

Minimum 3–5 years of hands-on experience in motion control system design and development in a high-tech or industrial environment.

Proven experience with servo drive systems, motion controllers, and real-time control platforms (e.g. Beckhoff TwinCAT, Siemens SIMOTION, National Instruments, or equivalent).

Strong knowledge of control theory: PID tuning, feed-forward control, frequency-domain analysis, and system identification.

Experience with dynamic modelling and simulation tools such as MATLAB/Simulink.

Familiarity with industrial communication protocols: EtherCAT, PROFINET, CANopen, or Modbus.

Experience in the semiconductor, analytical instruments, or medical device industry is a strong advantage.

Programming experience in C, C++, Python, or IEC 61131-3 (Structured Text, Ladder Logic).

Desirable Skill Set

Experience with precision positioning systems (sub-micron accuracy), wafer handling, or lithography stages. Knowledge of vibration analysis, structural dynamics, and active vibration isolation.

Familiarity with machine safety standards (ISO 13849, IEC 62061, IEC 61508).

Experience with robotics, collaborative robots (cobots), or multi-axis gantry systems.

Knowledge of Industry 4.0, digital twin technologies, and condition monitoring.

Proficiency in CAD software (e.g. SolidWorks) for mechanical integration reviews.

Experience working within Agile Scrum or Kanban teams. Worked with version control systems such as Git (GitLab, GitHub, Bitbucket).

Desirable Soft Skills

A preference for autonomy and responsibility in organizing your own work.

Good communication skills and ability to work effectively within a geographically distributed team.

A pro-active attitude with a focus on continuous improvement.

Good leadership skills are preferable.

WHAT WE CAN OFFER

Our employees are our strength and together we want to achieve the maximum. That is why we invest a lot in our employees, through generous development budgets and personal attention. According to our employees, this is what makes the difference at Sioux. We are proud of that. For us, success is more than just a good salary: it is also about feeling valued, getting responsibilities, and to be able continuously develop oneself.

• Internal training, coaching, and a generous development budget of 5000 SGD/ per year

• Varied work due to the diversity in technologies, markets, and projects

• Competitive salary, AWS, and variable bonus

• An open culture that focuses on collaboration, learning, and having fun

• An innovative work environment

Job Location

Our office is conveniently located next to the Tai Seng MRT station.

Position summary

Act as a technical expert in healthcare quality and regulatory analytics. Combine advanced quantitative analysis, data engineering, and quality system expertise to build stakeholder-specific reporting, develop AI-enabled quality tools, and integrate/manage third-party quality applications to support compliance, continuous improvement, and executive decision-making.

Key responsibilities (primary)

• Perform advanced quantitative data analysis: build statistical and machine learning models for trend detection, root-cause analysis, forecasting, anomaly detection, and risk stratification

• Design, build, and maintain stakeholder-specific dashboards and reports (executive, regulatory) using Power BI tools and data visualization best practices; deliver actionable insights and data storytelling.

• Develop and maintain quality tools and automations using AI/ML/LLM technologies (NLP for document classification/summarization, automated quality checks,

predictive analytics, chat assistants for SOP/QMS guidance).

• Lead integration and lifecycle management of third-party quality software: requirements gathering, vendor coordination, configuration, data integration, testing, release coordination, and ongoing support.

• Utilize current and emerging technologies in evaluating trends to business models and healthcare quality processes

• Develop insights and translate information into actionable initiatives to ensure business outcomes

• Lead and support projects through the application of technical expertise including conceptualization, planning, design, implementation and support of quality assurance processes, systems, and quality technology solutions

• Evaluate and monitor healthcare quality processes and systems to identify areas for continuous improvement and transformation ensuring global excellence

• Initiate and lead the development of reports for key stakeholders, including executive management, using data storytelling and visualization.

• Develop and execute tools to enhance services and deliver training for internal customers or vendors on analytics outputs, tools, and integrated systems.

• Gather and consolidate regulatory and business requirements into convert them into technical specifications and implement monitoring to ensure ongoing compliance with company’s internal policies and relevant regional and local regulations.

• Develop and maintain data validation, models, and metadata; routinely assess model performance and recalibrate as required.

• Lead end-to-end analytics projects: planning, stakeholder alignment, implementation, and post-implementation reviews; document methods and SOPs.

• Support audit readiness and provide analytics-driven evidence for regulatory submissions, inspections, and internal quality reviews.

• Identify opportunities for process improvement and automation in quality workflows, pilot new technologies and scale successful solutions.

Additional responsibilities (as needed)

• Provide subject-matter expertise for cross-functional programs and global initiatives.

• Manage vendor relationships and service-level expectations for third-party tools.

• Participate in career progression and mentoring for junior analysts.

Required skills and experience

• Bachelor's degree in Statistics, Data Science, Biostatistics, Engineering, Computer Science, Information Technology, Healthcare Analytics, or related field (or equivalent experience).

• Strong quantitative and statistical skills; proficiency in data science libraries and tools

• Experience building dashboards and visualizations with tools such as Power BI, Tableau, Looker, or equivalent.

• Hands-on experience integrating and managing third-party quality/GxP systems (MasterControl, Synthesis, ServiceNow) or similar QMS/issue tracking platforms.

• Experience working with cloud platforms, databases (SQL, NoSQL), ETL tools, and APIs.

• Practical experience applying AI/ML and prompt engineering for LLMs to automate quality processes, extract insights from unstructured documents, or create assistant workflows.

• Strong data validation, data modeling, and data governance understanding.

• Excellent communication and data storytelling skills; able to translate technical findings into concise recommendations for executives.

• Experience in a regulated environment (healthcare, life sciences, medical devices, or similar) strongly preferred.

• Demonstrated ability to work cross-functionally and manage vendor/IT relationships.

Preferred

• Certifications in data analytics, machine learning, or quality management.

• Prior experience with global operations or multi-regional regulatory frameworks.

Level expectations and experience guidelines

• 3-4 years relevant experience; independently manages projects and provides expert input, recognized expert, leads complex programs with high autonomy.

Core competencies

• Analytical thinking, accuracy, attention to detail, numerical skills.

• Planning and organizing, project management, stakeholder alignment.

• Statistical knowledge, data modeling, visualization skills, automation

• Vendor and cross-functional collaboration, training and documentation abilities.

Technical requirements

• Proficiency with Microsoft Office and web-based applications.

• Familiarity with automation and orchestration tools; experience deploying AI/ML models into production.

• Language: strong written and spoken English.

Compliance and other

• Ensure ongoing compliance with company processes, regional/local legislation, and external regulations.

• May be required to perform other duties as assigned; role can involve regional and global activities

Working Hours:

Mon to Fri 9am - 6pm ( 1 day hybrid )

Info can be shared ATM: -

• Basic UP $4K (W Exp) + AWS + VB
• 5 Days office hours
• Loyang

Your Responsibilities: -

• Maintain and update documents and records on ISO 9001, ISO 14001 and ISO 13485 system
• Conduct & liaise internal and external audits
• Generate monthly report/summary of OQA rejects, customer returns, RMA, external & internal 8D, revised specs and procedures.
• Review and update Quality Management System procedures to meet the quality system requirements.
• Manage internal and external corrective action reports (CAR)
• Plan and conduct periodic system audits and participate in customer or supplier audits for compliance.
• Maintain and conduct regular review of calibration and preventive maintenance for instruments and equipment

You will need: -

• Min. 1 years of relevant working experience
• Possess knowledge of ISO 9001, ISO 14001 & ISO 13485 quality system

Email to kennyho@recruitlync.com
Good Luck! Only shortlisted candidates would be notified.
Ho Tze Chin (Kenny) R1762905 | Recruit Lync Pte Ltd 22C1000