Total 64 test engineer job vacancies in Singapore

Position Overview:

We are looking for an experienced Mechanical Engineer with expertise in data centres and critical facilities projects. The successful candidate will be responsible for the design, implementation, and management of mechanical systems that ensure the optimal functioning of high-demand environments.

Key Responsibilities:

• Design and manage mechanical systems for data centres and critical facilities.
• Collaborate with project teams to ensure the integration of mechanical systems with electrical and HVAC systems.
• Oversee the installation and commissioning of mechanical systems to ensure quality and reliability.
• Ensure compliance with industry standards and safety regulations.
• Provide technical support throughout the project lifecycle, from planning to completion.

Qualifications:

• Bachelor’s degree in Mechanical Engineering or related field.
• Min 5 years of experience working on data centres and critical facilities projects.
• Proficiency in relevant mechanical design software (e.g., AutoCAD, Revit, HVAC tools).
• Strong knowledge of industry standards for mechanical systems in critical environments.
• Excellent problem-solving and communication skills.

To Apply, kindly click on the "APPLY NOW" button and job details. We regret that only shortlisted candidates will be notified.

Daniel Lim | Registration Number: R24124455 | AlwaysHired Pte Ltd

EA Licence No: 24C2293

Why Us?

• Basic + Commission
• Monday to Friday; 9am - 6pm
• Working Location: Aljunied Road

The Role:

• B2B sales to Hospitality and Education sectors for Pro Audio Solutions in Large Venues like Theater, Auditorium, etc.
• Generate new opportunities to closing.
• Work closely with renowned Audio partners and in-house AV Designer Team to propose solutions to meet customer’s needs.
• Negotiate pricing with partners to ensure bids are competitive.
• Present and submit weekly sales report
• Assist in Managing partners (Manufacturers) for Audio solutions and related solutions.
• Source and secure partnerships for Audio related solutions to increase the breadth of solutions to the same customer

What are we looking for?

• Experience in B2B sales with good sales track record
• Experience in Audio & Visual, videoconferencing, telephony solutions is a plus

Next Step:

Please submit your updated resume in MS Word format by clicking the QUICK APPLY button.

We regret to inform that only shortlisted candidates will be notified. Please note that your response to this advertisement will constitute informed consent to the collection, use and/ or disclosure of personal data by AlwaysHired and its affiliates for the purpose of job application processing and administrative purpose, in compliance with the relevant provision of personal data protection act.

Edmund Chung Keng Loon
Registration Number: R1986801
AlwaysHired Pte Ltd
EA Licence No: 24C2293

Job description:

• Supervising construction activities and monitoring progress, including planning, implementation, and adherence to master and detailed work schedules.
• Collaborating with Professional Engineers regarding Temporary works.
• Coordinating with consultants (QPS) to address technical issues and align site activities with subcontractors.
• Handling technical and engineering challenges as they arise.
• Providing guidance to supervisors regarding construction tasks, ensuring adherence to schedules, maintenance of quality standards, conducting site inspections, and timely resolution of technical issues.
• Preparing reports and method statements as needed.
• Managing and overseeing workers, closely monitoring their activities to maintain site safety and cleanliness.
• Supervising ongoing site activities diligently.

Job requirements

• Diploma / Degree in Civil Engineering or Recognised Degree in the relevant field subject.
• Min. 3 yrs experience in the construction site / LTA project

To Apply, kindly click on the "APPLY NOW" button and job details. We regret that only shortlisted candidates will be notified.

Daniel Lim | Registration Number: R24124455 | AlwaysHired Pte Ltd

EA Licence No: 24C2293

Job duties:

• Dealing with electronic/electrical equipment installation
• Testing, installing, & commissioning electronic/electrical equipment
• Maintaining electrical & instrumentation equipment
• Conducting calibrations & improving maintenance procedures
• Giving right instructions on proper usage of electrical installations
• Maintaining cleaning of industrial laundry equipment
• Inspecting engine room & utilizing right tools
• Experience as electrical engineer

Working location: West

Salary up to $3500 + AWS + Variable bonus

Interested candidates please apply online or send your latest CV to [email protected]

Kindly note that only shortlisted candidates will be notified.

AlwaysHired Pte Ltd

Reg No: R1441412

EA: 24C2293

RESPONSIBILITIES

• Provide after-sales service support, installation, commissioning and repair of laboratory/ research/ analytical equipment
• Provide technical consultation to customers
• To respond to customers’ requests by troubleshooting problems and take corrective actions within targeted timeline
• To prepare service reports

REQUIREMENTS

• ITE/Higher NITEC/Diploma/Degree in Electronics, Electrical, Mechanical Engineering or equivalent
• Able to work independently and a team player
• Excellent communication and interpersonal skills
• Self-motivated, results-oriented individual with good business acumen
• Minimum 3 years of related work experience in service / maintenance
• Valid Class 3 driving license and personal vehicle will be an added advantage

BENEFITS

• Attractive remuneration package
• Career development opportunities
• Five day work week
• Medical benefits

To Apply, kindly click on the "APPLY NOW" button and job details. We regret that only shortlisted candidates will be notified.

AlwaysHired Pte Ltd (24C2293) | Tan Jun Xi (Jonathan) (R1440473)

Responsibilities:

• Perform risk-based commissioning, qualification and validation service for pharmaceutical and biopharmaceutical clients on one or more of the following areas:Process Equipment
  CIP / SIP
  Process Manufacturing and related business processes including Quality Operations and Supply Chain Operations
  Method validation (analytical chemistry, biochemistry, microbiological)
  Enterprise system (LIMS, QMS)
  
• Develop risk assessment, system impact assessments, protocols and reports that support the qualification and validation requirements in the industry.
• Develop validation protocols using a science and risk -based approach that meets regulatory requirements and industry best practices.
• Review, analyse, interpret, and summarize system and process performance data of executed activities for report and presentation to management.
• Investigate deviations, write investigation reports and create summary reports.
• Exercise good judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions.

Professional Skills and Experience:

• Bachelor’s degree in technical discipline such as Engineering, Pharmaceutical Science or with experience relevant.
• Minimum 2 - 3 or more years of experience in several functions in pharmaceutical industry: commissioning, qualification, validation, quality systems, quality operations, manufacturing, engineering, technology transfer.
• Foundational understanding of ICH Q7, Q8, ICH Q9, ISO 14644, ANSI Z1.4 and other regulatory requirements preferred
• Experience with investigations into manufacturing / laboratory deviations and determination of product impact potential, root cause and corrective/preventive actions.
• Knowledge of Validation Lifecycle approach (URS, FAT/SAT, commissioning, I/O/PQ Protocols, etc), guidelines, international regulatory requirements and other industry best practices.
• Preferred to have experiences in multiple CQV discipline (such as CIP, SIP, process, utility, equipment, automation, computer system, lab system), preferably with advanced technical knowledge in one or more discipline.
• Preferred to have experience interacting with or creating material for management and regulatory agencies.

Interested candidates please apply online or send your latest CV to [email protected]

AlwaysHired Pte Ltd

Reg No: R1549345

EA: 24C2293

Responsibilities:

• Provide Computerized System Validation (CSV) / Computerized System Assurance (CSA) consulting services for pharmaceutical and medical device Manufacturing company.
• Manage SDLC (system design life cycle) including risk, deviation and change managements (e.g., conduct risk impact or functional assessment(s))
• Ensure Good Documentation Practices, working with policy and procedural governances, assessments, plans, reports etc.
• Develop and execute FAT/SAT test scripts, qualification protocols and reports based on industry best practices and Client’s / Solution Provider’s documentation system.
• Review, analyze and evaluate system functions and processes to deliver validation deliverables.
• Develop approach using science- or risk -based approach that meets regulatory expectation.
• If a Senior member of the team, serve as Lead for CSV service in one or more of the following disciplines:
• Production/Manufacturing System (e.g., MES, DCS, Historian)
• Laboratory Instruments/Equipment/Enterprise system (e.g., LIMS, Empower)
• Engineering/Automation (e.g., BMS, Delta V)
• Emerging technologies (e.g., SaaS platforms, Cloud system)

Requirement:

• Bachelor’s degree in technical discipline such as Engineering, Science or IT. Graduates of related discipline may also apply.
• Possess 2 or more years of experience performing CSV activities.
• Experience in engineering / process automation such as DCS, Delta V, Historian, MES and/or PLC would be viewed favorably
• Ability to communicate quality and risk-related concept to technical and non-technical audiences

Interested candidates please apply online or send your latest CV to [email protected]

AlwaysHired Pte Ltd

Reg No: R1549345

EA: 24C2293

Responsibilities:

• Perform risk-based commissioning, qualification and validation service for pharmaceutical and biopharmaceutical clients on one or more of the following areas:Process Equipment
  CIP / SIP
  Process Manufacturing and related business processes including Quality Operations and Supply Chain Operations
  Method validation (analytical chemistry, biochemistry, microbiological)
  Enterprise system (LIMS, QMS)
  
• Develop risk assessment, system impact assessments, protocols and reports that support the qualification and validation requirements in the industry.
• Develop validation protocols using a science and risk -based approach that meets regulatory requirements and industry best practices.
• Review, analyse, interpret, and summarize system and process performance data of executed activities for report and presentation to management.
• Investigate deviations, write investigation reports and create summary reports.
• Exercise good judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions.

Professional Skills and Experience:

• Bachelor’s degree in technical discipline such as Engineering, Pharmaceutical Science or with experience relevant.
• Minimum 2 - 3 or more years of experience in several functions in pharmaceutical industry: commissioning, qualification, validation, quality systems, quality operations, manufacturing, engineering, technology transfer.
• Foundational understanding of ICH Q7, Q8, ICH Q9, ISO 14644, ANSI Z1.4 and other regulatory requirements preferred
• Experience with investigations into manufacturing / laboratory deviations and determination of product impact potential, root cause and corrective/preventive actions.
• Knowledge of Validation Lifecycle approach (URS, FAT/SAT, commissioning, I/O/PQ Protocols, etc), guidelines, international regulatory requirements and other industry best practices.
• Preferred to have experiences in multiple CQV discipline (such as CIP, SIP, process, utility, equipment, automation, computer system, lab system), preferably with advanced technical knowledge in one or more discipline.
• Preferred to have experience interacting with or creating material for management and regulatory agencies.

Interested candidates please apply online or send your latest CV to [email protected]

AlwaysHired Pte Ltd

Reg No: R1549345

EA: 24C2293

Responsibilities:

• Perform risk-based commissioning, qualification and validation service for pharmaceutical and biopharmaceutical clients on one or more of the following areas:

1. Process Equipment
2. CIP / SIP
3. Process Manufacturing and related business processes including Quality Operations and Supply Chain Operations
4. Method validation (analytical chemistry, biochemistry, microbiological)
5. Enterprise system (LIMS, QMS)

• Develop risk assessment, system impact assessments, protocols and reports that support the qualification and validation requirements in the industry.
• Develop validation protocols using a science and risk -based approach that meets regulatory requirements and industry best practices.
• Review, analyse, interpret, and summarize system and process performance data of executed activities for report and presentation to management.
• Investigate deviations, write investigation reports and create summary reports.
• Exercise good judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions.

Professional Skills and Experience:

• Bachelor’s degree in technical discipline such as Engineering, Pharmaceutical Science or with experience relevant.
• Minimum 2 - 3 or more years of experience in several functions in pharmaceutical industry: commissioning, qualification, validation, quality systems, quality operations, manufacturing, engineering, technology transfer.
• Foundational understanding of ICH Q7, Q8, ICH Q9, ISO 14644, ANSI Z1.4 and other regulatory requirements preferred
• Experience with investigations into manufacturing / laboratory deviations and determination of product impact potential, root cause and corrective/preventive actions.
• Knowledge of Validation Lifecycle approach (URS, FAT/SAT, commissioning, I/O/PQ Protocols, etc), guidelines, international regulatory requirements and other industry best practices.
• Preferred to have experiences in multiple CQV discipline (such as CIP, SIP, process, utility, equipment, automation, computer system, lab system), preferably with advanced technical knowledge in one or more discipline.
• Preferred to have experience interacting with or creating material for management and regulatory agencies.

Interested candidates please apply online or send your latest CV to [email protected]

AlwaysHired Pte Ltd

Reg No: R1549345

EA: 24C2293

Responsibilities:

• Perform risk-based commissioning, qualification and validation service for pharmaceutical and biopharmaceutical clients on one or more of the following areas:Process Equipment
  CIP / SIP
  Process Manufacturing and related business processes including Quality Operations and Supply Chain Operations
  Method validation (analytical chemistry, biochemistry, microbiological)
  Enterprise system (LIMS, QMS)
  
• Develop risk assessment, system impact assessments, protocols and reports that support the qualification and validation requirements in the industry.
• Develop validation protocols using a science and risk -based approach that meets regulatory requirements and industry best practices.
• Review, analyse, interpret, and summarize system and process performance data of executed activities for report and presentation to management.
• Investigate deviations, write investigation reports and create summary reports.
• Exercise good judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions.

Professional Skills and Experience:

• Bachelor’s degree in technical discipline such as Engineering, Pharmaceutical Science or with experience relevant.
• Minimum 2 - 3 or more years of experience in several functions in pharmaceutical industry: commissioning, qualification, validation, quality systems, quality operations, manufacturing, engineering, technology transfer.
• Foundational understanding of ICH Q7, Q8, ICH Q9, ISO 14644, ANSI Z1.4 and other regulatory requirements preferred
• Experience with investigations into manufacturing / laboratory deviations and determination of product impact potential, root cause and corrective/preventive actions.
• Knowledge of Validation Lifecycle approach (URS, FAT/SAT, commissioning, I/O/PQ Protocols, etc), guidelines, international regulatory requirements and other industry best practices.
• Preferred to have experiences in multiple CQV discipline (such as CIP, SIP, process, utility, equipment, automation, computer system, lab system), preferably with advanced technical knowledge in one or more discipline.
• Preferred to have experience interacting with or creating material for management and regulatory agencies.

Interested candidates please apply online or send your latest CV to [email protected]

AlwaysHired Pte Ltd

Reg No: R1549345

EA: 24C2293

Responsibilities:

• Perform risk-based commissioning, qualification and validation service for pharmaceutical and biopharmaceutical clients on one or more of the following areas:

1. Process Equipment
2. CIP / SIP
3. Process Manufacturing and related business processes including Quality Operations and Supply Chain Operations
4. Method validation (analytical chemistry, biochemistry, microbiological)
5. Enterprise system (LIMS, QMS)

• Develop risk assessment, system impact assessments, protocols and reports that support the qualification and validation requirements in the industry.
• Develop validation protocols using a science and risk -based approach that meets regulatory requirements and industry best practices.
• Review, analyse, interpret, and summarize system and process performance data of executed activities for report and presentation to management.
• Investigate deviations, write investigation reports and create summary reports.
• Exercise good judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions.

Professional Skills and Experience:

• Bachelor’s degree in technical discipline such as Engineering, Pharmaceutical Science or with experience relevant.
• Minimum 2 - 3 or more years of experience in several functions in pharmaceutical industry: commissioning, qualification, validation, quality systems, quality operations, manufacturing, engineering, technology transfer.
• Foundational understanding of ICH Q7, Q8, ICH Q9, ISO 14644, ANSI Z1.4 and other regulatory requirements preferred
• Experience with investigations into manufacturing / laboratory deviations and determination of product impact potential, root cause and corrective/preventive actions.
• Knowledge of Validation Lifecycle approach (URS, FAT/SAT, commissioning, I/O/PQ Protocols, etc), guidelines, international regulatory requirements and other industry best practices.
• Preferred to have experiences in multiple CQV discipline (such as CIP, SIP, process, utility, equipment, automation, computer system, lab system), preferably with advanced technical knowledge in one or more discipline.
• Preferred to have experience interacting with or creating material for management and regulatory agencies.

Interested candidates please apply online or send your latest CV to [email protected]

AlwaysHired Pte Ltd

Reg No: R1549345

EA: 24C2293

Responsibilities:

• Perform risk-based commissioning, qualification and validation service for pharmaceutical and biopharmaceutical clients on one or more of the following areas:

1. Process Equipment
2. CIP / SIP
3. Process Manufacturing and related business processes including Quality Operations and Supply Chain Operations
4. Method validation (analytical chemistry, biochemistry, microbiological)
5. Enterprise system (LIMS, QMS)

• Develop risk assessment, system impact assessments, protocols and reports that support the qualification and validation requirements in the industry.
• Develop validation protocols using a science and risk -based approach that meets regulatory requirements and industry best practices.
• Review, analyse, interpret, and summarize system and process performance data of executed activities for report and presentation to management.
• Investigate deviations, write investigation reports and create summary reports.
• Exercise good judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions.

Professional Skills and Experience:

• Bachelor’s degree in technical discipline such as Engineering, Pharmaceutical Science or with experience relevant.
• Minimum 2 - 3 or more years of experience in several functions in pharmaceutical industry: commissioning, qualification, validation, quality systems, quality operations, manufacturing, engineering, technology transfer.
• Foundational understanding of ICH Q7, Q8, ICH Q9, ISO 14644, ANSI Z1.4 and other regulatory requirements preferred
• Experience with investigations into manufacturing / laboratory deviations and determination of product impact potential, root cause and corrective/preventive actions.
• Knowledge of Validation Lifecycle approach (URS, FAT/SAT, commissioning, I/O/PQ Protocols, etc), guidelines, international regulatory requirements and other industry best practices.
• Preferred to have experiences in multiple CQV discipline (such as CIP, SIP, process, utility, equipment, automation, computer system, lab system), preferably with advanced technical knowledge in one or more discipline.
• Preferred to have experience interacting with or creating material for management and regulatory agencies.

Interested candidates please apply online or send your latest CV to [email protected]

AlwaysHired Pte Ltd

Reg No: R1549345

EA: 24C2293

Responsibilities:

Carry out Bump Mask Design tasks to meet customer requirements and making sure that design outputs are aligned to bumping design guidelines and capability

• Design-need to consider all aspect to optimize layout for best possible product performance, consider impact to yield and minimize final product cost
• Responsible for the Design output and need to be in proper Bump Mask Tooling format with accurate information and promptly reviewed and approved by authorized UTAC personnel and customer
• To ensure proper documentation and maintenance of his/her design outputs according to UTAC design verification procedure
• Proficient with Auto-Cad with at least 3 years working experience using ACAD for Bump Mask Design
• Background on IC packaging / assembly processes and experience in using Cadence APD / Allegro or other PCB/ laminate substrate design software is an added advantage

Requirements:

• Degree in Engineering/Science
• Minimum 3 years' experience in Bump Mask Design with knowledge of bumping processes
• Strong understanding of bumping technologies, materials, and equipment
• Proven experience in process development, optimization, and troubleshooting
• Excellent analytical and problem-solving skills
• Ability to work effectively both independently and as part of a team
• Strong communication and interpersonal skills
• Attention to detail and commitment to quality
• Knowledge of industry standards and best practices

Interested candidates please apply online or send your latest CV to [email protected]

AlwaysHired Pte Ltd

Reg No: R1549345

EA: 24C2293

Job Description:

As a Test Engineer, you will play a pivotal role in designing and implementing ATE test solutions for IC manufacturing.

Responsibilities:

• Designing and implementing ATE test solutions for final test and/or wafer sort products, ensuring conformity to device electrical test specifications.
• Developing hardware and software solutions to enable IC testing, encompassing test program development, hardware development, and tester and multisite conversion.
• Conducting test time reduction activities, supporting engineering evaluations, and performing administrative tasks to facilitate test development.
• Supporting the hardware and software bring-up, debugging, and improvement of ATE IC testing.
• Engaging in engineering qualification, correlation, device characterization, and dry run activities with minimal supervision.
• Analyzing data and generating reports for engineering qualification, correlation, device characterization, and dry run purposes.
• Contributing to cost reduction projects such as tester and multisite conversion, program optimization, and yield improvement.
• Ensuring the seamless release of products from the engineering phase to mass production.
• Executing administrative tasks to support the test development team.

Requirements:

• Bachelor's Degree in Engineering, preferably in Electronics and/or Electrical.
• 2 years of experience working with Teradyne (ETS, UltraFlex, J750) and Advantest (V93K) testers.
• Familiarity with semiconductor ICs, test methodologies, and the test development process.
• Proficiency in programming languages such as C/C++, VB/VBA, LabVIEW, and scripting.
• Experience in hardware design and software development is advantageous.
• Experience in hardware and software troubleshooting is beneficial.

Interested candidates please apply online or send your latest CV to [email protected]

Kindly note that only shortlisted candidates will be notified.

AlwaysHired Pte Ltd

Reg No: R1549345

EA: 24C2293