Total 3,442 Others level Quality Assurance / Control job vacancies

about the company

My client is a specialized manufacturer in the contract manufacturing space. They are a Singapore based company and with their innovative technology, this is a great brand to join at an exciting time in their development.

about the job

• Plan, coordinate and oversee all Quality Assurance activities in the Company
• Oversee the Documentation Control function for Quality Management System
• Act as the Quality Management Representative for the Company
• Develop and implement plans to collect quality data at in-process, final inspection, test and inspection stations
• Plan and execute annual Internal Audit to ensure all quality systems and procedures are effectively implemented and auditable at all times
• Develop and implement system for receipt and processing of complaints and recall of products
• Participate in all new Projects, including giving inputs from quality perspectives, performing PFMEA etc

job requirement

• Degree in Engineering or equivalent
• Manufacturing background from plastics injection medtech manufacturing environment
• Must possess ISO13485 certification

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

Job Title: Quality Assurance Technician
Location: Pioneer
Working Hours: Mon to Fri 8.30am -5.30pm
Basic Salary: $2000 to $3000

Key Responsibilities
• Provide stone-like product sample boards to Sales as required
• Develop colour matching formulas through testing and paint manufacturing processes
• Prepare colour-matching formulas for stone-like products and wet samples for the Production team
• Maintain and control all stone-like product formulations and update records in collaboration with the Technical team
• Set up standard formula for new stone like products
• Color-match flat paint for sample board and wet sample orders
• Report nonconformities or deviations to supervisors
Other Tasks
• Support the Display Controller during her absence
• Carry out system maintenance and updates for the colour matching machine
• Act as safety supervisor for Warehouse and Display areas during toolbox meetings and related activities
• Maintain cleanliness and organization of the Display Lab and office area
• Adhere to company quality procedures, work instructions, and safety requirements
• Ensure compliance with applicable ISO standards and internal quality systems

Requirements
• Minimum GCE N / O Level or equivalent
• Ability to follow procedures and maintain accurate documentation
• Strong attention to detail
• Good communication and teamwork skills

Salt is looking to hire QA Analyst for a big technology client in Singapore for 12 months & renewable contract role. The QA analyst will develop and execute software test plans in order to identify software problems and their causes.

Description:

• Design test plans, scenarios, scripts or procedures.
• Test system modifications to prepare for implementation.
• Develop testing programs that addresses areas such as database impacts, software scenarios, or usability.
• Document software defects, using a bug tracking system, and report defects to software developers.
• Identify, analyze and document problems with program function, output, online screen or content.
• Monitor bug resolution efforts and track successes.
• Create or maintain databases of known test defects.
• Plan test schedules or strategies in accordance with project scope or delivery dates.

Qualification:

• 5-7 experience as a QA Analyst working in automation
• Verbal and written communication skills, problem solving skills, customer service and interpersonal skills.
• Basic ability to work independently and manage one’s time.
• Basic knowledge of QA automation
• Basic knowledge of the practical application of engineering science and technology.
• Basic knowledge of computer development software such as JavaScript, SQL, etc.

CEI No: R1659595 / EA No: 07C3147

Job Responsibilities:

• Implement QA plan, review, and revision for company level.

• Report on quality related matters to the QA/QC Manager and/orimmediate superior, including preparation of monthly summary Tocreate, prepare and implement the QA/QC plan and any associatedand relevant directives and instructions needed to support Todevelop and manage the quality control and quality assuranceprocedures and ensure compliance.

• To prepare Inspection and Test Plan (ITP) and Inspection ReportsMaintain the ISO and related certifications for company level.

• To perform needed tests on site to ensure works are doneaccording to the contract specifications. Preparation of documentsubmissions for client approval.

• Attend meetings and liaise with the client to ensure that qualityrequirements are being followed at all times.

• Maintain document record master list pertaining to equipmentand monitor on the calibration status. Coordinate and makearrangements for equipment calibration when due.

• Compile and receive relevant material certificates and otherrequired certificates and test report from vendors/suppliers.Coordinate with relevant testing laboratories for testing andwitnessing.

• Compile and maintain quality records e.g. Request for Inspection(RFI) and verify as necessary. Coordinate on-site quality assuranceand control activities.

• To conduct independent Quality Assurance check on and off site.

• Report non-conformities to the QA/QC Manager and/or ProjectManager, perform analysis, identify root cause and proposecorrective actions.

• Maintain and control QA/QC practices on daily basis with regularchecks and inspections ensuring correct operation andimplementation of procedures.

• Advise and assist the project team members on QA/QC matters.Assist in the development of internal QA/QC checklists.

• Implement and enforce Quality Control Plan.

• Verification and checks on raw/incoming materials and/or FG.Documents for non-conforming works and corrective action.

• Identify and assess any foreseeable risk arising from workplace orwork processes, minimize environmental impact associated withthe manufacturing / assembly activities.

• Perform other duties as and when assigned/instructed byimmediate superior or higher management.

Job Requirements:

• Minimum Qualification: Diploma in Mechanical/Electrical orMarine Engineering Discipline Minimum 1-2 years of experience inMarine, Oil & Gas Industry

• Welding Certificate

• Good understanding of Marine/Offshore industry practices andstandards.

• Know-how in one or more of these areas GD&T, NDT, welding,steel fabrication, material casting, and machining technology willbe preferred.

• Familiar with ISO 9001 requirements & different marineclassification societies' standards and requirements will be anadded good knowledge of QMS and ability to implement, conductchecks and audit and upkeeping of documents etc.

• Project Management Skills

• A team player with good interpersonal and communication skills,attention to details, meticulous and independent. Goodorganizational, multitasking, prioritization, and effective timemanagement skills.

• Ability to think critically and resolve problems/issues. Positiveattitude, proactive and self-initiated.

• Ability to multi-task in a fast paced and dynamic environment

Job Responsibilities:

• Provide leadership and guidance to nursing staff, promoting best practices in patient care and infection prevention

• Support recruitment, onboarding, and development of nursing personnel to maintain strong clinical standards

• Work with doctors, allied health professionals, and department teams to implement evidence-based clinical practices

• Ensure compliance with regulatory standards, patient safety requirements, and quality care practices

• Monitor clinical indicators and patient outcomes to identify improvement opportunities

• Lead quality improvement initiatives aimed at enhancing patient safety and care delivery

• Develop and deliver training, orientation, and continuing education programmes for nursing staff

• Provide mentorship and supervision to support professional development within the nursing team

• Monitor infection control data, conduct surveillance, and support outbreak management when required

• Develop infection prevention protocols and ensure compliance with infection control procedures

• Support committee activities, audits, and regulatory processes related to infection control

Requirements:

• Bachelor’s Degree in Nursing with relevant certification in Infection Control preferred

• Registered Nurse with valid registration with Singapore Nursing Board

• Minimum 5 years of clinical nursing experience with exposure to infection control practices

• Strong leadership, communication, and stakeholder management skills
  

  
  

Interested candidates are invited to email your resume to:

jen.ooi@recruitexpress.com.sg
Jenalyn Ooi Huai Sian (R1765551)
Recruit Express Pte Ltd | Company Reg. No. 199601303W | EA License Number: 99C4599

• Consolidate and summarize fuel consumption data across the entire ONE fleet
• Support fuel saving initiatives and decarbonisation activities
• Conduct comprehensive analysis and reporting on fuel consumption and vessel performance
• Research and evaluate new vendors and emerging technologies for vessel modifications and efficiency upgrades
• Monitor the utilization for energy saving devices
• Maintain regular condition checks for D/G and Boilers to ensure optimal performance and early detection of abnormalities
• Conduct research and propose new technical solutions or vendors to enhance fleet efficiency.
• Support in any ad hoc tasks and projects as assigned

Interested candidates, please email your resume to annasee@recruitexpress.com.sg

Anna See Sing Yee

CEI Reg R25157535

Recruit Express Pte Ltd

EA License No: 99C4599

We regret that only shortlisted candidates will be contacted

Responsibilities:

• Monitor the quality of machining activities
• Report quality of machining activities and proposed solution.
• Propose & implement process changes to improve quality
• Implement surveillance activities relating to quality for external and internal machining activities
• Receive materials and reviews supplier documentation to determine dimension specifications, measurements, and tests required to ensure quality and customer satisfaction.
• Performs SAP transactions after completion of QC operations.
• Assists during internal/external audits (API, ISO, and customer).

Requirements:

• 3 years of hands-on experience as Quality Control in related industries.
• Able to understand and interpret complex blueprints/technical/engineering drawings.
• Able to perform inspection using precision measuring equipment.
• Good interpersonal and communication skills.

Responsibilities:

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

Qualifications:

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

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

Wecruit Pte Ltd

EA License No: 20C0270

EA Personnel: Nyon Hock Sen (Aden)

EA Personnel Reg No: R24124070

Responsibilities

•  Review project documentation, customer demands, and product objectives to understand the software application under test.
•  Develop comprehensive test plans that can validate both functional and non-functional requirements of the application prior to its release to end-users.
•  Execute test cases, recording any issues or defects encountered during testing.
•  Collaborate with developers, project managers, and other stakeholders to identify and resolve issues.
•  Communicate testing results and issues clearly and effectively to all stakeholders.
•  Stay up to date with emerging trends and technologies in software testing and quality assurance.
•  Participate in the development and implementation of testing frameworks, methodologies, and tools.
•  Provide feedback on product design and functionality to improve the overall user experience.
• Work with Test Manager to support UAT session
• Perform Manual edge testing

Requirements

• Minimum 2-3 years of experience in software quality assurance.
• Strong understanding of QA methodologies and experience with software development lifecycle.
• Proficient in programming for white-box testing, and familiar with grey-box and black-box testing.
• Good understanding of coding and programming standards for JavaScript and Python.
• Proficient in written and spoken English.
• Excellent communication and teamwork skills.
• Strong organizational and methodical skills, with the ability to handle multitasking.
• Capable of executing both manual and automated test suites throughout the project cycle.
• Ability to identify and report discrepancies discovered during testing, and to compose test reports.
• Proficient in setting up and configuring testing environments and data.
• Willingness to contribute to team improvement initiatives and projects, including testing tools, process improvements, and test automation.
• Proficient in implementing and maintaining test scripts, shell scripts, and testing tools for automation purposes and test coverage improvements.
• Detail-oriented with an eye for details.

JOB DESCRIPTION :                    

1.   Be able to do 8D reports arising from the customers' complaints.             

2.   Issue and provide COC to the customers.               

3.   Co-ordinate customers' audits or site visits for customer qualification or quality issues.          

4.   Able to manage and facilitate company's ISO9001-2015 systems and reporting.           

5.   Communicate and provide customer service to potential and existing customers.           

REQUIREMENT   :     

 -   Diploma or Degree in Engineering                

 -   Prefer minimum 2 years working experience in electronic industry.          

 -   Proactive and great team player and able to work efficiently with minimal supervision.                        

 -   Good customer service skills.                 

Interested applicants are invited to submit your updated CV to haidee@ccd.com.sg

QEHS Consultant

ISO Consultants Pte. Ltd. (ICPL)

Position

QEHS Consultant (Quality, Environmental, Health & Safety)

Employment Type

Full-Time

Location

Singapore

About ICPL

ISO Consultants Pte. Ltd. (ICPL) is a Singapore-based consultancy specialising in ISO standards, cybersecurity, sustainability, governance, risk and compliance. We support organisations across diverse industries in achieving certification, regulatory compliance and continual improvement objectives.

Key Responsibilities

Consultancy & Implementation

• Lead and support ISO 9001, ISO 14001 and ISO 45001 consultancy projects.
• Conduct gap assessments and implementation reviews.
• Develop management system documentation including manuals, policies, procedures, forms and registers.
• Facilitate workshops, training sessions and management reviews.
• Support clients throughout certification readiness activities.

Audit & Compliance

• Conduct internal audits against applicable standards.
• Prepare audit reports and corrective action plans.
• Monitor closure of findings and improvement actions.
• Support certification audits and regulatory compliance activities.

Project Management

• Manage project timelines, deliverables and client communications.
• Coordinate with consultants, clients and certification bodies.
• Maintain project records and status reports.

Business Development Support

• Participate in client meetings and presentations.
• Support proposal preparation and project planning.
• Maintain positive client relationships.

Requirements

Education

• Diploma or Degree in Engineering, Environmental Science, Occupational Safety & Health, Quality Management or related discipline.

Experience

• Minimum 2 years of relevant experience in consultancy, auditing, compliance or management systems.
• Experience in one or more of the following:ISO 9001ISO 14001ISO 45001bizSAFE

Preferred Qualifications

• Internal Auditor or Lead Auditor certification.
• Knowledge of Singapore regulatory requirements.
• Experience in construction, engineering, manufacturing, logistics, marine, facilities management or service industries.

Competencies

• Strong written and verbal communication skills.
• Analytical and problem-solving abilities.
• Ability to manage multiple projects simultaneously.
• Proficiency in Microsoft Office applications.
• Ability to conduct client engagements independently.

Benefits

• Professional development and certification opportunities.
• Exposure to diverse industries and projects.
• Career progression opportunities.
• Flexible and collaborative work environment.
• Performance-based incentives.

Responsibilities:

• Drive after-sales quality tasks and drive product improvements
• Lead Product Quality Circles with sustaining teams, platform leads, and HODs
• Serve as central coordinator and support for improvement teams
• Manage escalations (NPI or customer-related) in after-sales
• Join customer quality calls and task force meetings
• Coordinate cross-functional quality circles, lead documentation, escalation and customer communication.
• Collaborate with product line and technical support to share field learnings and build preventive knowledge
• Own project documentation and communication (8D reports, action plans, follow-ups)
• Initiate and support product analysis; liaise closely with production facility
• Participate in customer audits and improvement programs
• Prepare after-sales data, monitor KPIs, and report results

Requirements:

• Minimum Degree in Mechanical, Electrical, Mechatronics, Machining or related field
• 3 years of relevant working experience and knowledge of project management / quality tools
• Strong understanding of reliability methods (DFMEA, SPC, 8Ds) and semiconductor manufacturing
• Experienced in quality methods, data analysis, and continuous improvement
• Able to drive improvements and navigate company structure with multiple interfaces
• Knowledge of product-related processes (design, engineering, SCM, production)
• Familiar with cleanroom protocols (Class 10/100) and semiconductor workflows
• Proficient in MS Office for analysis, reporting, and presentations

Interested candidates who wish to apply for the advertised position, please click on the APPLY button below to send in your resume or send to engg1@talenttradersg.com

EA License No: 13C6305

Reg. No.: R24121656 (CHEN JING WEI)

For candidate who applied for the advertised position is deemed to have consented to us that we may collect, use or disclose your personal information for purpose in connection with the services provided by us.

Senior QC Analyst (Microbiology/ Pharma/ Contract)

12 Months Contract

Location : Gul Circle (5 mins walk from MRT)

Basic Salary : Up to $5,500 depending on experience

Industry : Pharmaceutical

Responsibilities

• Executing analytical testing in a timely manner, ensuring adherence to the committed scheduled plans
• Performing his/ her tasks in accordance with cGMP and HSE requirements, and with the associated instructions, procedures, records, related to these tasks
• Recording all expected raw data, calculations, information, related to his/her tasks, to comply with cGMP and data integrity requirements
• Ensuring that is trained and qualified to the assigned analytical testing that requires to be qualified
• Performing the QC data review of executed tests by other analysts in a timely manner, ensuring adherence to the committed scheduled plans
• Informing his/her manager of any quality or HSE event (deviations, OOx,…) in a timely manner to ensure investigation and impact assessment are performed appropriately
• Participating actively to any investigation, where is involved, to ensure investigations and impact assessment are performed appropriately
• Executing assigned CAPAs related to remediation plans, continuous improvements
• Ensuring that his/her lab/facilities, lab instruments are kept in a quality and safety status to ensure that they can be used appropriately.
• Owning assigned stability studies, in compliance with approved stability program
• Ensuring the issuance and review of all deliverables related to assigned stability studies, such as risk assessment, protocols, reports, data trending, deviations, and summary reports
• Ensuring that sampling and testing related to stability is executed in a timely manner and stability results trend performed on time, including reports issuance
• Ensuring that all expected stability data (including events, change control…) are compiled in a proper way, to provide appropriate data trending and statistical analysis of stability studies, in compliance with associated stability protocols

Additional Accountabilities

• Review analytical results and perform audit trail review before batch release.
• Carry out on-the-job training for General and Specific Analytical Method to QC analysts and chemical technicians, by incorporating cGMP and safety aspects of the procedures.
• Perform troubleshooting of equipment in the laboratory and provide guidance to QC analysts on the troubleshooting.
• Trained and work independently on specific testing method
• Ensure availability of workplace risk assessment and safe working procedures for contractors and the quality personnel. Ensure safe working in all areas of work by practicing and communicating safety message at +QDCI Sanofi Manufacturing System (SMS) Awareness, Life Saving Rules (LSR), GMP/Data Integrity Awareness
• Other responsibilities that are not included in the above are related to quality assignments.

Lim Pey Chyi (Apple) - Apple.lim@manpower.com.sg

Recruitment Consultant (R2090579)

Manpower Staffing Services (S) Pte Ltd

EA Licence: 02C3423

Documentation & Quality Records

Prepare, maintain, and organize QA/QC documentation for ongoing projects.

Ensure inspection records, reports, and quality-related documents are properly filed, updated, and maintained.

Prepare material submittals, inspection checklists, test reports, and handover documentation.

Maintain document control for drawings, method statements, technical submissions, and project records.

Track and monitor material certificates, calibration certificates, and testing reports for compliance and traceability purposes.

QA/QC Coordination

Coordinate with project, engineering, production, and site teams for submission and collection of QA/QC records and documents.

Support QA/QC Engineers during inspections, audits, and quality-related activities.

Ensure documentation complies with client requirements, project specifications, and company quality procedures.

Compliance & Audit Support

Ensure proper record traceability and compliance with company quality management procedures.

Assist in maintaining quality procedures, forms, templates, and standard documentation.

Reporting & Administrative Support

Prepare weekly and monthly QA/QC reports and quality tracking updates.

Maintain and update quality logs, document registers, and monitoring records.

Ensure proper filing and organization of both softcopy and hardcopy QA/QC documents.

Perform other ad-hoc QA/QC administrative and coordination duties assigned by management.

Decommissioning Engineer (Validation/ Qualification/ Contract/ Pharma)

6 Month Contract

Industry : Pharmaceutical

Location : Tuas

Up to $9,500 depending on experience

Company transport provided

Responsibilities:

• Assist Lead Engineers/Managers in completing work activities in a timely and effective manner, in compliance with GMP/ EHS requirements.
• Coordinate with the planner and ensure decommissioning activities for equipment and Utility/Facility areas are carried out by technicians according to the approved plan.
• Coordinate with vendors for the execution of decommissioning activities for equipment and Utilities/ Facility.
• Manage change controls and impact assessments in collaboration with stakeholders.
• Support calibration activities; prior experience in calibration
• Experience with the SAP Plant Maintenance module 
• Perform EHS actions identified during GEMBA walkdowns, PHA, and similar assessments.
• Perform any other duties as assigned by the Manager.

Requirements:

• At least 3 years of experience in validation or qualification or Commissioning or decommissioning experience within manufacturing industry
• GMP experience

Lim Pey Chyi – Apple.lim@manpower.com.sg

Recruitment Consultant (R2090579)

Manpower Staffing Services (S) Pte Ltd

EA Licence: 02C3423