Total 4,838 Quality Assurance / Control job vacancies in islandwide

Our client is a leading player in food service industry. They are looking for a Accounts Receivable Executive to assist their team for the next phase of their business. They are located in North.

Duties:

• Implement and monitor credit control procedures, ensuring timely payment and resolving outstanding balances.
• Process customer credit applications, create debtor codes, and manage credit terms using SAP.
• Track and chase overdue payments via calls and emails; negotiate payment plans when necessary.
• Prepare and submit monthly debtors aging reports; update sales teams on overdue accounts.
• Oversee the issuance of Customer Statements monthly.
• Handle bank transactions such as cash and cheque deposits, and manage customer-related AR requests.

Requirements:

• Min Diploma in Accounting or related field.
• Minimum 3 years of experience.

Interested candidates who wish to apply for the advertised position, please click APPLY NOW or email an updated copy of your resume/cv. We regret that only shortlisted candidate will be notified.

• Email address: [email protected]
• Recruitpedia Pte. Ltd.
• EA License No: 19C9682
• EA Reg. No. R23118456 (Law Yi Xin)

Our client is from Medical industry. They are looking for a Software Engineer to assist their team for the next phase of their business. They are located in Central - easily assessable.

Duties Software QA Engineer:

• Verify user applications and server-side components to meet requirements and specifications discreetly.
• Execute Unit, Regression, Integration, Performance, and System Tests confidentially.
• Collaborate with developers to resolve issues arising from test procedures and results while maintaining confidentiality.
• Take ownership of assigned modules and projects discreetly.
• Manage defect tracking and implement solutions confidentially.
• Update tasks in OpenProject privately.
• Maintain and backup databases as needed, ensuring data security discreetly.
• Participate in software design reviews and create confidential test reports for releases.
• Review software documentation for technical accuracy while maintaining confidentiality.

Requirements:

• Diploma/ Degree in IT or Computer Science.
• Min 3 years of working experience in relevant industry
• Experience in SQL, JENKINS and TestComplete

Interested candidates who wish to apply for the advertised position, please click APPLY NOW or email an updated copy of your resume/cv.

We regret that only shortlisted candidate will be notified.

Email Address: [email protected]

Recruitpedia Pte. Ltd.

EA License No. 19C9682
EA Reg. No. R22108850 (Chan Mun Mun)

Do you dream of working in a company that is driven by a meaningful purpose? An inclusive company that empowers you to do your best and be innovative?

We are a looking for Senior Quality Assurance/Quality Control (QA/QC) Engineer to make an impact! In this role, you will be accountable to build and drive the quality processes, execution and teams for its Data Centre projects in APAC. You will work closely with the project sponsors and project management team to define the project objectives, create a plan for executing those objectives. Dependant on the systems demand, the role will include working on multiple projects or directly on a single specific project in APAC.

At Schneider Electric, we believe access to energy and digital is a basic human right. We empower all to do more with less, ensuring Life Is On everywhere, for everyone, at every moment. We provide energy and automation digital solutions for efficiency and sustainability.

What will you do?

• Ensure Quality-related activities on the Project are compliance to Corporate, Project, and other applicable Regulatory requirements.
• Implement BIM360 QA/QC dashboards to show overall KPI metrics and status, and manage documentation tracking, distribution and submission through various collaboration tools.
• Generate Project high-level Plans/Guidelines to provide roadmap for key Quality related activities.
• Ensure knowledge transfer / lessons learnt of execution issues to local customer & SE teams. Ensure compliance to overall program.
• Ensure adequate and suitably qualified Quality team resources are available to support Project Quality requirements.
• Involve in Project Review in conjunction with Engineering/Construction phases of the Project and ensure appropriate closure of observations/issues raised from review, generation of final review closeout report.
• Ensure Project SOP’s/Plans/Guidelines are appropriately authorized for implementation and adequate training provided.
• Develop, implement and manage an effective Audit Schedule focusing on the key work processes, and design activities undertaken during the project lifespan.
• Review and approve Quality Records/Reports, Engineering Drawings, Change Notices/Design Modifications, Quality Plans, Inspection Test Plans, etc.
• Conduct and maintain training program for relevant project personnel for Project SOP’s/GDP/GEP applications.
• Continually identify and proactively manage project risks and issues, ensure execution of corrective action plans up to closure.
• Implement systematic documentation turnover system for all Project Quality related documentation.
• Manage day-to-day activities of the Project walk down teams.
• Plan, prepare, review and execute project system walk down packs to transfer punch items into Master Punch list database (BIM360), approval and issuance of Construction Completion Certificate.
• Provide support and advice on Quality-related issues and resolution of engineering-related disputes.
• Responsible for any other related QAQC matters as requested by management.
• Be seen as the trusted advisor for our customer.

What qualifications will make you successful?

In this role practical experience will carry a high weighting than formal qualifications: -

• Bachelor’s Degree in Engineering or any other related discipline from recognized university.
• Minimum of 5 years of relevant work experience in BMS, HVAC, or Industrial Controls / Automation industry.
• Has an excellent working knowledge of the technical and operational environment in which the project deliverables are created and in which they are used.
• Must be an excellent communicator at all levels both internal and external in the project environment, be proactive and exhibit strong leadership qualities and be able to adapt to a dynamic and geographically disbursed environment.
• Position is to be base at client’s site.

What's in it for me?

• Global Family Leave
• Comprehensive medical coverage for employee and dependants
• Worldwide Employee Stock Ownership
• ...... and more!

Let us learn about you! Apply today.

Job Description

• Position: QC Engineer
• Well Established Singapore Based Manufacturing MNC
• Working hours: Monday – Friday (8:30am – 6:00pm)
• Salary (commensurate with experience): Up to $4,500
• Working Location: Ang Mo Kio
• Outpatient Medical Insurance Provided
• Duration: Permanent
• Industry: Manufacturing

Main Responsibilities:

• Working with Process Engineer & Engineering team on QC requirement.
• Documenting inspection criteria and quality plan.
• Work with QA, Process and Product team on corrective action with quality issue.
• Work with Process team on in-process audit and FQC audit.
• Control of Supplier Quality Assurance (SQA).
• Quality control of in-coming, in-process and out-going products.

Requirements:

• Minimum Diploma in Manufacturing / Quality Engineering.
• At least 1 year of relevant working experience in Electronics Product Manufacturing environment.
• Knowledge of ISO 9001, 14001, 13485 & 45001, FDA requirement.
• Able to understand IPC requirement in PCB Assembly, quality requirement of plastic molding, die casting, extrusion, metal stamping and machining parts.
• Able to converse with in Mandarin fluently as it is required to liaise with China suppliers.

Email to: [email protected] for more information.

***We do not charge our candidates any referral fee nor bind them with any contract. ***

Henry Heng

Consulting Manager

Reg no.: R1982999

EA No: 20C0257

The QA/QC Engineer is responsible for implementing site quality assurance and quality control system, in compliance with the quality standards at site.

A summary of the responsibilities of this position are, and not limited to, as follows:

• Engage the project team to deliver high quality works;
• Lead the QA/QC team and train the site team on Structural and Architectural trades;
• Assess site operations and procedures daily and recommend improvement actions;
• Provide insights for defects and recommend preventive measures;
• Prepare monthly reports for Management;
• Conduct Internal Quality Audits;
• Compile trade information, test reports, and formalize documentation;
• Liaise with authorities (i.e. BCA on assessment to achieve target score, LTA on inspections and compliances)
• Adhere to safety practices in the workplace.

Value Add of Position

• Obtain buy-in from project team towards quality assurance and quality control initiatives.
• Translate deep understanding of quality standards and requirements into site works.

Qualifications and Education Requirements

• Education: Degree in Civil Engineering or construction related field
• Experience: At least 3 years of building and/or civil engineering experience.
• Experience in QA/QC and certified auditors would have an added advantage.
• Completed at least 1 building project

Technical Competencies

• Knowledge of quality requirement of BCA, industry norms and contract specifications
• Quality Management Systems certification – ISO 9000
• Knowledge in Structural and Architectural works

To provide quality support to the Clinical Storage and Distribution facility in Singapore in line with PIC/S Good Manufacturing Practice and Good Distribution Practice. (GMP and GDP)

SPECIFIC DUTIES, ACTIVITIES AND RESPONSIBILITIES

General :

• Perform review and release of materials, including therapeutic products intended for clinical trials and packaging components.
• Provide support on Quality matters to Project Management / Operations in the area of clinical packaging, storage and distribution.
• Evaluate CAPA effectiveness and identify process improvements.
• Review and approval of Change Control, Complaints, and Deviation reports.
• Monitor closure of corrective and preventive actions from client audit, regulatory inspections, complaints, non-conformances and deviations.
• Manage site SOP System, including review, update and approval of SOPs.
• Approve specifications, sampling instructions and other Quality Control procedures.
• Review and approval of validation/ qualification documents.

Authorized Person Responsibility:

• Perform review and approval of batch records (pre-execution and post-execution) to ensure compliance with applicable regulations and guidelines.
• Perform batch certification in accordance with the principles detailed in Annex 16 of the PIC/S GMP Guide, and any other applicable guidelines or regulations.

Audits:

• Coordinate client audits and regulatory inspections.
• Ensure timely consolidation and provision of response reports for client audits and regulatory inspections.
• Perform supplier qualification, including audit of external suppliers and contractors.

Requirements

• Min Diploma / Degree in any science / engineering courses
• Min 2 to 3 years of quality experience in pharma / medical device manufacturing / clinical storage industry

Salary range: $3.5K to $4K

Office Hours

Interested candidates, please forward your resume to [email protected]

Consultant: Huang Jingsheng Kevyn (R1333338)

Recruit Express Pte Ltd (99C4599)

Our client is a global MNC, one of the most established pioneers in the Chemical industry. Due to business needs, they are now recruiting a QA Assistant Manager / Manager to be part of their QA Team for ongoing transformation projects. They are located in the West - easily accessible.

Duties of QA Assistant Manager / Manager:

• Oversee QA processes for raw materials, in-process items, finished products, and packaging.
• Collaborate with the Head of Production to set and uphold quality standards.
• Develop and maintain an effective Quality Management System (QMS), including documentation, audits, and improvement initiatives.
• Provide inter-departmental support and ensure effective communication on quality-related issues.
• Lead the Quality Assurance Task Force to investigate and resolve product non-compliances.
• Manage maintenance and calibration of QA equipment.
• Evaluate monitoring records and process operation parameters.
• Handle material failure reviews and follow up on disposal decisions.
• Review out-of-specification product parameters and authorize fit-for-purpose decisions.
• Implement actions to prevent product nonconformity.
• Identify and document product quality issues.
• Ensure adherence to 5S, safety, and security standards in the workplace.
• Perform other duties as assigned.

Requirements:

• Diploma / Degree in related field
• Relevant experience

Interested candidates who wish to apply for the advertised position, please click APPLY NOW or email an updated copy of your resume/cv.

We regret that only shortlisted candidate will be notified

• Email Address: [email protected]
• EA License No: 19C9682
• EA Personnel No: R2199158
• EA Personnel Name: Soo Wei De

Our client is a well-established MNC, market leader in the Medical industry. They are looking for a QC Executive to assist their Lab team for the next phrase of their business. They are located in Town – easily accessible. The QC Executive is responsible for:

Duties

• Managing quality control, equipment, reagents, and store operations.
• Ensures all staff adhere to CSG SOPs and procedures.
• Performing and documenting quality control for products, reagents, equipment, calibration, and maintenance.
• Responsible for procuring reagents and materials, assisting in CSG tasks to meet goals, and monitoring QC performance according to regulatory standards.
• Performing validation studies as needed, preparing for audits, and compiling IQC, EQAS, and proficiency testing records.

Requirements

• Min Diploma in Biomedical sciences with 1 year experience
• Experience in ISO Class 10000 lab environment

Interested candidates who wish to apply for the advertised position, please click APPLY NOW or email an updated copy of your resume/cv.

We regret that only shortlisted candidate will be notified.

Email Address: [email protected]

Recruitpedia Pte. Ltd.

EA License No: 19C9682

EA Reg. No. R23115141 (Tan Su Yee)

Our team ensures that all trading activities adhere to regulatory and internal policies whilst mitigating risks associated with market integrity. We monitor transactions and provide guidance on compliance issues whilst collaborating with various stakeholders to promote a culture of ethical practices within the organization.

As a Fixed Income - Compliance, Associate in a line of business Compliance team covering Fixed Income, Currency and Commodities (FICC) , you will be centrally involved in all aspects of the financial product sales and trading. You will work as part of a team that provide credible challenges and give advice to internal stakeholders on the impact of regulatory requirements. You’ll also provide input on new business strategies, product lines, policies and education, operational processes, risk mitigation and control. This role will have a specific focus on assisting the regional FICC Compliance team covering Credit business, which has its significant presence across Asia locations.

Job responsibilities:

• Ensure compliance coverage responsibility for the FICC business regionally, with a general focus on Credit

• Continuously assess regulatory and compliance risks inherent in existing and proposed business activities and initiate, coordinate and deliver process enhancements where required

• Dealing with regulatory updates, development and inquiries in the region

• Liaising with Global Compliance counterparts in order to communicate APAC issues as well as stay abreast of global initiatives

• Reviewing new products and initiatives from Compliance perspective

• Assisting in the design, development, implementation and ongoing operation of the Compliance program

• Preparing and delivering Compliance training materials across Asia

• Drafting and manage the roll out of Compliance policies, procedures and guidelines and any associated requirements

• Liaising with country and corporate compliance groups as well as other corporate control functions such as Operations, Technology, Finance, Tax and Legal as required

Required qualifications, capabilities, and skills :

• Bachelor’s Degree in Finance, Economics or other related disciplines

• Minimum 5 years of experience within a securities firm, bank or an equivalent financial institution in the Asia Pacific Region, with experience in FICC products

• Familiarity with FICC business and knowledge of related regulations

• Excellent communication, interpersonal and influencing skills, with the ability to establish credibility and partnership with senior business leaders

• Analytical, problem-solving and organizational skills, as well as the ability to manage several simultaneous projects

• Ability to multi-task, prioritize and project manage complex issues

• Ability to work independently and as part of a team

• Inquisitive with a keen eye for detail

To apply for this position, please use the following URL:

https://ars2.equest.com/?response_id=c027ed9747ea6d0866175b6313aaddec

Preclinical QA Specialist (QMS/ Test Facility Management)

Our client is a GLP-compliant and AAALAC accredited, preclinical CRO based in Singapore. They offer a range of preclinical services, from GLP toxicology safety assessments, aerosol generation and delivery to research support services to help achieve research goals. We are currently looking for a Preclinical QA Specialist to support the operations.

More information

• Location: Central
• 5 Days Work
• Up to $6,500 depending on experience

Job Summary

• Responsible for applying a local Quality Assurance program for the R&D Test Facility in alignment with Good Laboratory Practice (GLP), other applicable regulations and company best practices.
• To assure Test Facility Management (TFM) and management that the facilities and studies are in compliance with Good Laboratory Practice regulations.
• Supports the implementation of ISO 17025 and other applicable standards pertinent to non-clinical research and/or toxicological assessments in order to verify that the studies are performed in accordance with the applicable regulatory frameworks, QMS requirements and best practices.
• Supports the quality oversight of suppliers and contract laboratories for pre-clinical research and/or toxicological assessments, as well as to identify opportunities for quality and process improvements in pre-clinical development.

Responsibilities

• Plan, perform and report QA inspections and suppliers audits to assure TFM and management that procedures/standards are in compliance with relevant national and international requirements for GLP/ISO 17025 for both internal and external entities. Monitor and follow up on corrective actions and preventive actions (CAPAs) reporting in response to internal audits and regulatory inspections.
• Support the monitoring of pre-clinical studies throughout their conduct and reporting for compliance with the GLP principles.
• Support the review of test report for ISO 17025 documentation and support management review and other relevant activities.
• Support R&D Test Facility for inspection readiness, participating in regulatory inspections/accreditations, and managing the corrective and preventive actions (CAPAs) reporting in response to internal audits and regulatory inspections
• Provide administrative support for the QMS document/record/training management system, including QA review of records such as QMS documents (SOPs/WKIs/Forms), Training, Nonconformance (NC), Corrective Action Preventive Action (CAPA) and Lab Change Request (LCR) for key QMS processes. Provide regular training on the systems and QMS (e.g. Good Documentation Practice, GLP and ISO 17025) for new and existing staff.
• Manage the archival process in accordance with established SOP and GLP principles
• Monitor and report quality key Performance Indicators (KPI) during Quality Management Review (QMR)
• Perform QA review of equipment/instrument qualification plans, reports and related documentation for GLP activities, to assure that the laboratory equipment/instrument are suitable for their intended purposes
• Continue to be developed as an expert in understanding GLP/ISO 17025 compliance on a global basis including local compliance enforcement experience with Health Authorities

Requirements:

• Bachelor degree in scientific discipline (Life Sciences, Biology, Chemistry etc) or equivalent
• Minimum 3 years of work experience in a laboratory environment (chemical/biologic analyses) and participation in quality assurance related activities in tobacco, food, pharmaceutical or similar industry and/or at least 3 years experience as a specialist in a relevant area of activity.
• Experience in quality standards e.g. ISO 170205
• Working knowledge of OECD principles of Good Laboratory Practice, knowledge of other quality systems such as FDA GLP Principles, cGMP, ISO, GCP and AAALAC

Lim Pey Chyi (Apple) - [email protected]

Recruitment Consultant (R2090579)

Manpower Staffing Services (S) Pte Ltd

EA Licence: 02C3423

Job Highlights

• Permanent Position
• Competitive salary and benefits package
• Opportunity to work on exciting and challenging projects
• Great opportunities for learning & career advancement

Responsibilities:

• Carry out repair and rectification of equipment failure and malfunction.
• Test and recommission rectified systems or equipment.
• Perform overhaul, inspection, calibration, and servicing programs during plant scheduled outages.
• Implement modifications, upgrades, and installation plans for plant systems and equipment to enhance availability and reliability.
• Maintain detailed work reports, spreadsheets, and graphs using computer-based software (Maximo, MS Word, MS Excel).
• Assist Engineers and Technical Officers in maintenance work.
• Supervise contractors under your charge.

Requirements:

• Nitec in Electronics Engineering or an equivalent qualification.
• Possess knowledge of instrumentation.
• Preferably have 2 years of experience in the Power Plant or Oil and Gas industry.
• Self-driven, with a good working attitude and a strong team player.
• Available on standby after office hours for emergency calls.

Interested applicants, please write in through CareersFuture with detailed resume in MS Words format

EA License Number: 23C1730

Please Provide:

1) Availability

2) Current/ Expected salary

3) Reasons for leaving previous employments

We regret that only shortlisted candidates will be notified.

Senior / Laboratory Assistant | 5 Days | Up to $3.2k | Jurong

Working Hours: 5days (Mon-Fri), 8 am to 4.30 pm.
Work location: Jurong Island (Transport provided at Jurong East
Salary : 1,900 to $3,200 + Site allowance

The Laboratory Assistant is responsible for conducting of laboratory tests and samples and quality inspections assigned to them by the Supervisor.
They are expected to be knowledgeable on all equipment operating procedures as well as all quality control procedures and competent on the use of laboratory equipment.

Other responsibilities include:

• Raw material process and finished product quality control analysis
• Advance maintenance, calibration and troubleshooting of assigned laboratory equipment
• Maintenance of chemicals and consumables inventory, preparation and standardization of chemical reagents and waste management.
• Maintenance of quality records and development of quality procedures
• Training of junior laboratory or chemical technicians
• Calibration of equipment
• Conduct and contribute to risk assessment, Quality Procedures and Decision making on quality & maintenance
• Procurement of materials and budget controls
• Implementing QA & Safety Activities

Requirement:

• 1 – 2 years or more than 5 years’ experience in conducting Manual Wet Chemistry or Manual Lab Testing.

The Supreme HR Advisory Pte Ltd | 14C7279

Ong Boon Kiet (Travys) | R22104769

Senior Recruitment Consultant

Monday - Friday 9am to 6pm, 9am to 1pm on Sat (Alternate)

Office Location: (Boon Lay)

Basic: $5000 to $5500 depending on the experience

Job Requirements

Minimum 5 years’ experience working in the Food industry and possess good knowledge of manufacturing processes.

Proven track record in leading the set-up and implementation of ISO22K or higher standards in the food manufacturing industry will be an added advantage.

Possess knowledge of international standards i.e. FSSC22K, GFSI

Min. Degree/Diploma in Food related discipline, Food Science or Food Technology

Job scope

Support functional departments in terms of processes of food quality and safety during daily operations.

Plan, organize, and coordinate to ensure the smooth operation of the QA Department daily.

Understand the business direction of the company and work closely with respective coaches to make necessary adjustments on job scopes and responsibilities to synchronize with the strategic plans of GM.

Prepare monthly reports i.e. Complaint Log, HACCP Objectives Summary, Demerit Point System Records, GMP audit, etc. for submission to the Management

Collect and analysis data/trend analysis report on non-conformity and improvement initiatives.

Plan lab testing by the sensitivity level of FG to manage and control department expenses and to keep within budget.

Participate and support quality system implementation (audit activities by government sectors, certification bodies, and customers)

Work closely with all functional departments on improvement initiatives i.e. standards, processes, and procedures in writing

Assign with short-term projects/initiatives/training programs and responsible for ensuring completion of work before the datelines.

Report all non-conformity matters regarding food quality or safety to the coach.

Other project as assigned

Whatsapp: +65 80135651(Alvin)

Alvin Chua Ming Jing:R23116192

The Supreme HR Advisory Pte Ltd: 14C7279

We are looking for Regulatory/QC/QA Lab Analyst to be outsourced to our clients from the healthcare industry.

Job Description:

• Conduct regulatory compliance assessments and ensured adherence to industry standards and guidelines.
• Managed administrative tasks related to quality control and assurance, including documentation and record-keeping.
• Performed laboratory analyses and testing to ensure product quality and compliance with established specifications.
• Coordinated with regulatory bodies and internal teams to address and resolve compliance issues and discrepancies.
• Reviewed and updated standard operating procedures (SOPs) and quality management systems to maintain accuracy and effectiveness.
• Assisted in the preparation of regulatory submissions and reports, ensuring all required information is complete and accurate.
• Monitored and reported on quality metrics, identifying trends and areas for improvement to support continuous quality enhancement.

Requirement:

• Minimum Diploma / Degree in Science (Boichemistry/Chemistry/Microbiology/Food Science/ Biotechnology/Life Science)
• Minimum 1 year experience / internships in lab settings preferred
• Detail-oriented with strong organizational and IT skills.
• Capable of executing tasks efficiently when given instructions.
• Self-driven, mature, and composed under pressure, with a strong sense of confidentiality and the ability to work independently with minimal supervision.

All qualified applicants, please send in your resume to:

[email protected]

Elyssa Koh (Outsourcing Team)

Jacqueline Fong Hsin Ting (R21103226)

Recruit Express Pte Ltd | Company Reg. No. 199601303W | EA License Number: 99C4599

Requirements

• Diploma with 2 years related working experience
• With Power BI will be advantage
• Knowledge of basic quality management systems and ISO9001
• Able to work independently and a team-player as well
• Meticulous and eye for details
• Well versed in both written and verbal communications skills

Responsibilities

• Provides administrative support by conducting research, preparing statistical reports and addressing routine to complex information requests
• Gathers, compiles and verifies information and enters it accurately into documents such as reports, presentations or forms e.g. databases or spreadsheets
• Data collection, data entry and report generation on various departmental related activities
• Preparing correspondence, receiving visitors, arranging conference calls and scheduling meetings
• Prepares documentation for payment of vendors, suppliers and other third parties
• Maintains departmental policies and procedures
• Facilitates, follows up on, and ensures completion of tasks related to the Quality Management System (QMS) including internal audits

Job Description

• Lead and manage the instrumentation, control and automation engineering and design works.
• Ensure instruments, electrical and control designs compliance with customer specifications.
• Lead the team to provide technical supports to all instrumentation, control and automation works.
• Collaboration with internal stakeholders, clients, consultants, vendors and contractors.
• Handle equipment package and procurement including technical specifications preparation, technical clarification, technical bid analysis, etc.
• Work with cross function project team to support project activities, i.e. schedule, process, progress claims, etc.
• Coordinate, provide direction and support to the project team.
• Manage and supervise the site installation, inspection, testing and commissioning, plant proving related to Instrumentation, Control and automation system and interface works with other disciplines and other stakeholders.
• Attend to clients’ comments and ensure clients’ approval & acceptance to all ICA related design, installation and Testing & Commissioning Works.

Requirements

• Degree in Electrical & Electronic Engineering / Instrumentation & Control Engineering / Advanced Diploma in Process Control and Instrumentation.
• At least 15 years of relevant experience
• Experience in Selection, installation and Commissioning of Instrumentation.
• Experience in system design, network design, installation and commissioning of the control and monitoring systems.
• Experience in Basic Programming of PLC/DCS and SCADA.
• Experience in Project Execution, Supervising and Coordination with sub-contractors, consultant and Client.
• Good technical knowledge in understanding instrumentation, control and automation system.
• Knowledge in electrical system and mechanical process system will be an advantage.
• Good technical understanding of water, wastewater and pollution control system.
• Relevant experience in design and site work for water and wastewater treatment works.
• Meticulous and analytical with excellent problem solving skills.
• Able to work under tight deadlines.
• Highly motivated and ability to work independently with minimal supervision.

Salary: up to $2500

Duration: 3 months

Working Days & Hours: Mon-Fri Office Hours

Location: Boon Lay

Job Description:

• • Assist the head of department in quality control of raw materials and finished products.
• • Verify and issue Certificate of Acceptance products that meet specified quality standards.
• • Conduct inspection of the raw materials and finished products through the use of analytical equipment.
• • Responsible for the proper use and maintenance of laboratory and analytical equipment.
• • Assist in customer complaints investigation.
• • Assist in inventory control and maintenance of laboratory apparatus and supplies.

Job Requirements: Min Diploma in Science or similar

Interested candidates, please submit your resume to: [email protected]

Ally Audrey Lok Xin Woon

Recruit Express Pte Ltd (Healthcare & Lifescience)

Company EA Licence number : 99C4599

Personnel EA License: R21102307

[email protected]

Job duties and responsibilities:

• Perform receiving inspection of spare parts, in-process inspection of
servicing/repair jobs and final inspections to vehicles & equipment,
• Ensure completeness of quality records and documentation,
• Monitor and ensure compliance to quality systems of operations,
• Applicants possess Class 4 driving license would be an advantage.

Requirements:

• Candidates must have at least NTC / Nitec in Automotive/Mechanical/ Electrical/ Electronic Engineering;

• Must have at least 3 years relevant experience.

We are looking for Business & Risk Control Manager

Responsibilities:

• Lead Business Control team, responsible for generating daily trading PnL for multiple trades (physical, paper & long term contract).
• nalyze PnL and identify movement factors; reconcile PnL with Accounting and Trader teams. 
• Communicate with management or traders regarding urgent risk topics. Support and lead crisis and issue management efforts in coordination with other teams and management.
• Managing Market Risk with counterparties including MTM calculation. 
• Analyze new deals, review contracts, and collaborate with traders on business planning and budgeting.  Conduct KYC for onboarding new counterparties; manage individual client credit ratings and monitor credit exposure. 
• Daily check broker reports and derivatives positions. 
• Update market information and pricing as needed. 
• Lead market risk analysis (VAR) and monitor portfolio based on respective stop loss limits, ensuring stop loss limits are implemented once breached.
• Build a strong Control team and establish control policy of all offices. It includes training, coaching and regular follow up with team members.

Requirements:

• 7 years of working experiences in Commodity trading firms, with non-ferrous metals experiences having an advantage. 
• Advanced skills in Excel 
• CPA, any major in Finance or business degree preferred. 
• Eye for details and a good understanding of Commodity trading company. 
• Good understanding of contractual laws, title transfer of cargo, payment terms and shipping terms. 
• Decent understanding on Commercial laws and crisis management. 
• Highly motivated and ready to take challenging position. 
• Excellent negotiation skills. 
• Team player who can develop harmonious relations in the Company 
• Compliance with Company and management’s directions and policies. 
• Excellent communication skills. Proficiency in Mandarin will be advantageous (dealing with China’s counterparts)

Responsibilities:

• Execute user acceptance testing activities according to defined test plans and procedures.
• Identify, document and track defects found during testing.
• Collaborate with project stakeholders to ensure test coverage and accuracy.
• Provide timely feedback to development teams on UAT defects.
• Assist in creation and maintenance of test cases and test data.
• Adhering to quality assurance standards and procedures throughout testing process phases.
• Ensure UAT are completed with scheduled timelines.
• Assisting on daily reports maintenance and other ad hoc duties as per assigned

Requirements:

• Previous experience in user acceptance testing is preferred.
• Strong attention to detail and ability to follow test procedures accurately.
• Ability to work independently and in a team environment.
• Excellent communication and collaboration skills
• Flexibility thinking in executing UAT.
• Willingness to learn.
• Familiarity with testing tools and methodologies is a plus.

Trade & Compliance Executive

Basic Salary: $2000 - 2500
Working hours: 9am-6pm (Mon-Fri)
Address: Cecil Street (Tanjong Pagar/ Telok Ayer MRT)

Job Description:

• Collaborate with cross-functional teams to enhance internal processes related to quotation speed, relevant shipping documents, inventory management (oversees WH), and supply chain planning in general
• To assist in quotation matters
• To liaise with partners on compliance matters
• To ensure compliant coordination between pricing and operations team
• To foster a culture of continuous learning and professional development within the team

Job Requirements:

• With relevant working experience is preferred.
• With Diploma in logistic / supply chain is preferred.
• Training Provided

WhatsApp: +65 9642 0989 (Han)

Email: [email protected]

Chaw Chiaw Han, Reg No：R22106723

The Supreme HR Advisory Pte Ltd, EA No：14c7279

Responsibilities:

• Specify project requirements and scope for contractors
• Oversee machine installation, testing, and commissioning, and resolve any issues
• Create detailed electrical diagrams and program industrial control systems
• Drive projects forward to meet deadlines and deliver results
• Coordinate and assist installation teams to ensure smooth execution"

Requirements:

• Diploma in Electrical/Electronics/Mechatronics Engineering or it's equivalent
• At least 3 years of related working experience
• Previous experience in PLC/SCADA & HMI is an added advantage
• Able to work in a team

Interested candidates who wish to apply for the advertised position, please send in your resume to [email protected]

EA License No: 13C6305

Reg. No.: R1874608

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.

Wipro Limited is a leading global information technology, consulting and business process services company. We harness the power of cognitive computing, hyper-automation, robotics, cloud, analytics and emerging technologies to help our clients adapt to the digital world and make them successful.

A company recognized globally for its comprehensive portfolio of services, strong commitment to sustainability and good corporate citizenship, we have over 220,000 dedicated employees serving clients across six continents. Together, we discover ideas and connect the dots to build a better and a bold new future.

QA Analyst, Manual Test Execution and Operational Support

The scope of Services for the Software Developer shall be as follows:

Manual QA:

• Engage with multiple stakeholders(Eng, PM, AM, Business etc) from the beginning, understand the business requirements and identify any potential quality gaps between the user requirements and product specifications.
• Write test scripts as per functional requirements of the new product/feature and ensure we build high quality products thinking through edge cases along with utilizing different quality signals like internal QA, user feedback etc to reduce SIT/UAT cycles.
• Manual QA test execution(One time) for new feature launches.
• As per product needs, provide support for additional types of non repetitive exploratory testing like mobile device coverage, localization(i18n), accessibility(a11y) etc.
• Be the voice of Quality via product launch readiness signals/metrics.
• Definition of Done: Post feature launch.
• Partner with eng to define P0 test cases to automate via e2e or integrated tests or implement necessary logging alerts to prevent future regressions.
• Partner with change management and documentation teams on release content docs.

Driving Quality Best Practices:

• Setup org wide Quality metrics and goals in partnership with Eng and other stakeholders.
• Introduce new process/advocate use of right tools/guidelines to drive QA programs.
• Drive org wide fixathon/testathons/optimizathon like quality/better eng related events in partnership with Eng teams.

We thank all applicants for your interest but regret to inform that only shortlisted candidates would be notified.

We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, caste, creed, religion, gender, marital status, age, ethnic and national origin, gender identity, gender expression, sexual orientation, political orientation, disability status, protected veteran status, or any other characteristic protected by law.

Salary: up to $4500 + allowances

Duration: 1 year contract

Working Days & Hours: 3223 12 hrs shift

Location: Tuas (islandwide pickup)

Job Description:

• To provide an effective testing and analytical service to the plant ensuring that products manufactured are tested

• to specification on time and plant quality and safety goals are met.

• Ensure that all raw material, in-process and finished product testing and method transfer testing is carried out per

• schedule and per gmp. Ensure that records are maintained to appropriate requirements.

Major Responsibilities:

• Responsible for housekeeping duties in the lab.

• Responsible for the timely completion of chemical testing of raw material, intermediates, in-process

• control samples and final API and data verification.

• Ensure that all test equipment is used and maintained correctly.

• Perform any method transfer or method qualification reports or equipment qualifications and support the

• transfer of new products.

• Maintain up-to-date, complete and precise records of all tests performed.

• Adhere to cGMP and GLP requirements and apply 6S concept.

• Assist in the resolution of quality problems as required.

• Developing and changing of in-house laboratory procedures as appropriate.

• Train new analyst.

• Support Audit preparation and any audit related activity

• Adheres to and supports all EHS & E standards, procedures and policies

• Any other general administrative duties/ad-hoc projects as assigned by immediate supervisor.

Job Requirements: Min Degree in Chemistry/Pharmaceutical Science/Biotechnology/Sciences or similar w min 3 yrs of relevant HPLC GC experience in Pharmaceutical industry

Interested candidates, please submit your resume to: [email protected]

Ally Audrey Lok Xin Woon

Recruit Express Pte Ltd (Healthcare & Lifescience)

Company EA Licence number : 99C4599

Personnel EA License: R21102307

[email protected]

Trade & Compliance Executive | Up to $2.5k | 5 Days | Tanjong Pagar

Basic Salary: $2000 - 2500
Working hours: 9am-6pm (Mon-Fri)
Address: Cecil Street (Tanjong Pagar/ Telok Ayer MRT)

Job Description:

• Collaborate with cross-functional teams to enhance internal processes related to quotation speed, relevant shipping documents, inventory management (oversees WH), and supply chain planning in general
• To assist in quotation matters
• To liaise with partners on compliance matters
• To ensure compliant coordination between pricing and operations team
• To foster a culture of continuous learning and professional development within the team

Job Requirements:

• With relevant working experience is preferred.
• With Diploma in logistic / supply chain is preferred.
• Training Provided

The Supreme HR Advisory Pte Ltd | 14C7279

Ong Boon Kiet (Travys) | R22104769

Senior Recruitment Consultant