16 Laboratory Equipment jobs in Singapore

Job Description
As an Equipment Engineer, you will own all assigned toolsets. The candidate can troubleshoot difficult and poorly defined problems related to mechanics, electronics, and processes using tool knowledge/experience, SPC, schematics, and other available resources. The candidate will collaborate extensively with the area maintenance team and process engineering. Some collaboration will be with tool vendors, other area engineers/managers, procurement, and production. Provide technical leadership and management of 200MM and 300MM Semiconductor processing equipment in Support of Main Stream Semiconductor Processes and Advanced Packaging processes. Highly desirable for a candidate to have a background in at least one of the following areas: Photolithography, PVD and CVD Thin Films, Dry Etch, Wet Etch /Wafer Clean, Diffusion, Bond, Electroplate (ECD), CMP, or Metrology (some areas may be combined).
Responsibilities
Work with process engineering to drive root-cause corrective actions for equipment failures, implement permanent solutions, and eliminate chronic and long-term down events.
Lead continuous improvement teams to drive tool matching, availability, and throughput improvements and reduce risk.
Management of new tool installation, start-up, and tool upgrades to increase fab capability and capacity, lower costs, and improve yields.
Work with minimal supervision, balancing competing priorities, to serve the needs of the Maintenance, Production, and Development organizations.
Participate in cross-functional teams that create efficiencies across all layers of the organization.
Job Requirements
Degree / Diploma with 10+ years of relevant Semiconductor Industry Experience in Mechanical, Electrical, or Chemical Engineering, Materials Science, Physics, or another relevant Engineering discipline.
6+ years of experience within the respective areas of expertise. Experience should include one or more: Semiconductor Wafer Handling, RF Power, High Vacuum, Toxic Gas Delivery systems, Precision Optics, and Wet Chemistry.
Demonstrated experience with the application of structured problem-solving methodology.
Positive interpersonal skills, highly energetic and self-motivated.
Experience with Automated Fault Detection and Classification Systems (FDC).
Strong background with utilizing SPC.
High level of understanding of equipment component behaviour.
Experience Integrating Equipment Maintenance Management Software
Demonstrated ability to meet requirements and deliver results.
Ability to manage and execute multiple projects simultaneously and shift priorities to meet business needs.
Seniority level
Associate
Employment type
Full-time
Job function
Engineering and Information Technology
Industries
Research Services
Johor Baharu, Johore, Malaysia
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• Salary range: $2000 - $3000 + Performance Bonus
• Working days & hours: 9:00am – 6:00pm (Monday – Friday)
• Working Location at Bukit Batok
• Well established Scientific and Laboratory Equipment Company

Job Scope

• Perform collection and delivery of instruments to and from customer sites.
• Conduct on-site evaluation, testing, troubleshooting, and basic repairs of equipment according to company procedures.
• Provide installation and commissioning support for instruments when required.
• Assist with in-house assembly of instrument parts in the laboratory.
• Coordinate closely with sales and service teams to ensure smooth customer support and after-sales service.
• Ensure proper handling, care, and documentation of equipment during transport and servicing.
• Comply with all workplace safety and risk assessment procedures.

Requirement

• NITEC in Engineering and above
• 0 – 2 years related experience in relevant position
• Possess Class 3 Driving License is mandatory

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

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

We regret that only shortlisted candidates will be contacted.

YEOW CHANG FU (R )

EA Recruitment Pte Ltd

EA License No: 21C0492

Due to our constant growth, we are looking for a Lab Validation Equipment / CQV Engineer to support a strategic decommissioning and qualification project in a GMP-regulated laboratory located in Singapore.

You will be responsible for:

• Supporting the decommissioning of analytical instruments in a GMP-regulated laboratory, ensuring compliance with internal procedures and regulatory standards.
• Managing the qualification workflow of laboratory equipment as needed, with hands-on involvement in protocols and reporting.
• Drafting and reviewing decommissioning protocols and related documentation, aligned with GMP requirements and client-specific templates.
• Collaborating with vendors, QA, and client stakeholders to ensure smooth execution of decommissioning and qualification activities.
• Ensuring all documentation and reports adhere to Data Integrity principles (ALCOA+), GAMP5 guidelines, and current GMP regulations.
• Providing technical support and oversight during execution of decommissioning tasks, including removal, data migration/archiving, and closure activities.

About You

• 5–7 years of experience in laboratory equipment validation/ CQV projects in GMP-regulated environments.
• Solid understanding of equipment lifecycle management , with specific experience in decommissioning activities .
• Background in usage, calibration, maintenance, and qualification/validation of analytical equipment and instrumentation used in biopharmaceutical QA, QC, R&D, or micro laboratory environments is required.
• Fluent in English (written and spoken); Mandarin Chinese is a nice-to-have.
• Strong communication and stakeholder management skills.
• Detail-oriented, organized, and capable of managing multiple tasks under tight timelines.
• Quality-driven mindset with strong ownership and accountability.

Responsibilities:

• Responsible for the selection/purchase, installation/commissioning, validation/calibration, maintenance, and repair of QC laboratory instruments
• Draft various procedures and technical documents related to instruments, participate in the maintenance and optimization of processes, and ensure their implementation;
• Conduct laboratory events and deviation investigations related to instrument management
• Initiate changes related to instrument management and track the timely execution of CAPA
• Assist analysts in troubleshooting during testing, and provide training on relevant skills when necessary
• Evaluate data integrity of various instrument systems and improve the department's level of data integrity
• Proactively study regulatory documents from various countries, such as CP, USP, JP, and EP, and refer to these documents when updating internal procedures
• Participate in customer audits and government inspections, promptly address identified issues, and ensure GMP compliance
• Timely track work progress, strengthen communication with internal and external clients, and establish stable and good relationships
• Assist department leaders in building a high-efficiency team.
• Perform any other ad hoc duties and responsibilities assigned by the Department Lead.

Requirements:

• Engineering, Pharmaceutical or Chemistry related major, bachelor's degree or above
• Understand pharmaceutical production, testing, and quality management; familiar with GMP regulations
• Prior experience in instrumentation companies (e.g., Agilent, Waters, Thermo Fisher, etc.) is strongly preferred.
• Proficient in English and Chinese, fluent in spoken English and Chinese to liaise with stakeholders from China and overseas, to support technical transfer.
• Good computer skills.
• Over 3 years of work experience in the management of analytical instruments; candidates with GMP instrument management experience will be given priority
• Proficient in analytical testing and quality management, familiar with the structure and working principles of analytical instruments
• Familiar with industry laws and regulations regarding technical specifications for analytical instruments
• Familiar with industry requirements for data integrity of analytical software; candidates with experience in computerized systems validation (CSV) will be given priority
• Strong ability to handle on-site issues, with good coordination, communication and execution skills
• Detail-oriented, proactive and able to work under pressure
• Ability to determine problems, gather information, understand facts and draw correct and effective conclusions through scientific reasoning
• Project management and tracking skills
• Ability to manage budgets and assets, controlling lab expenses
• This role required an on-the job training in China for approximately 3 to 6 months.

Working Location:

• Tuas, Singapore

Responsibilities:

• Responsible for the selection/purchase, installation/commissioning, validation/calibration, maintenance, and repair of QC laboratory instruments
• Draft various procedures and technical documents related to instruments, participate in the maintenance and optimization of processes, and ensure their implementation;
• Conduct laboratory events and deviation investigations related to instrument management
• Initiate changes related to instrument management and track the timely execution of CAPA
• Assist analysts in troubleshooting during testing, and provide training on relevant skills when necessary
• Evaluate data integrity of various instrument systems and improve the department's level of data integrity
• Proactively study regulatory documents from various countries, such as CP, USP, JP, and EP, and refer to these documents when updating internal procedures
• Participate in customer audits and government inspections, promptly address identified issues, and ensure GMP compliance
• Timely track work progress, strengthen communication with internal and external clients, and establish stable and good relationships
• Assist department leaders in building a high-efficiency team.
• Perform any other ad hoc duties and responsibilities assigned by the Department Lead.

Requirements:

• Engineering, Pharmaceutical or Chemistry related major, bachelor's degree or above
• Understand pharmaceutical production, testing, and quality management; familiar with GMP regulations
• Prior experience in instrumentation companies (e.g., Agilent, Waters, Thermo Fisher, etc.) is strongly preferred.
• Proficient in English and Chinese, fluent in spoken English and Chinese to liaise with stakeholders from China and overseas, to support technical transfer.
• Good computer skills.
• Over 3 years of work experience in the management of analytical instruments; candidates with GMP instrument management experience will be given priority
• Proficient in analytical testing and quality management, familiar with the structure and working principles of analytical instruments
• Familiar with industry laws and regulations regarding technical specifications for analytical instruments
• Familiar with industry requirements for data integrity of analytical software; candidates with experience in computerized systems validation (CSV) will be given priority
• Strong ability to handle on-site issues, with good coordination, communication and execution skills
• Detail-oriented, proactive and able to work under pressure
• Ability to determine problems, gather information, understand facts and draw correct and effective conclusions through scientific reasoning
• Project management and tracking skills
• Ability to manage budgets and assets, controlling lab expenses
• This role required an on-the job training in China for approximately 3 to 6 months.

Working Location:

• Tuas, Singapore

Due to our constant growth, we are looking for a Lab Validation Equipment / CQV Engineer to support a strategic decommissioning and qualification project in a GMP-regulated laboratory located in Singapore.

You will be responsible for:

• Supporting the decommissioning of analytical instruments in a GMP-regulated laboratory, ensuring compliance with internal procedures and regulatory standards.
• Managing the qualification workflow of laboratory equipment as needed, with hands-on involvement in protocols and reporting.
• Drafting and reviewing decommissioning protocols and related documentation, aligned with GMP requirements and client-specific templates.
• Collaborating with vendors, QA, and client stakeholders to ensure smooth execution of decommissioning and qualification activities.
• Ensuring all documentation and reports adhere to Data Integrity principles (ALCOA+), GAMP5 guidelines, and current GMP regulations.
• Providing technical support and oversight during execution of decommissioning tasks, including removal, data migration/archiving, and closure activities.

About You

• 5–7 years of experience in laboratory equipment validation/ CQV projects in GMP-regulated environments.
• Solid understanding of equipment lifecycle management , with specific experience in decommissioning activities .
• Background in usage, calibration, maintenance, and qualification/validation of analytical equipment and instrumentation used in biopharmaceutical QA, QC, R&D, or micro laboratory environments is required.
• Fluent in English (written and spoken); Mandarin Chinese is a nice-to-have.
• Strong communication and stakeholder management skills.
• Detail-oriented, organized, and capable of managing multiple tasks under tight timelines.
• Quality-driven mindset with strong ownership and accountability.

PES is an international services company providing Project Management, Construction Management, Commissioning & Qualification and Automation services to our clients in the pharmaceutical, nutritional and related sectors.

With offices across Europe, Asia and US, our core focus is on consistently delivering high-quality outcomes for our multinational clients.

This focus, and our people's experience in delivering consistent quality results for our clients over the past 20 years has been key to our success to date.

We are currently looking for Validation Engineers to join us on a permanent role to help us deliver various projects in the Life Sciences Industry.

Key Attributes/Responsibilities:

• Looking for candidates with 0-3 years validation/CQV experience.
• Using the process automation system for the commissioning and validation of process equipment.
• Protocol Development (IQ,OQ, PQ) / protocol review for process equipment.
• Interface with client personnel and with outside vendors when necessary while performing the above.
• Managing validation projects.
• Individual will manage all facets of assigned validation projects while maintaining strong communication with client representatives on project status and assistance needed.

We are currently looking for candidates in Singapore.

If you'd like to find out about this opportunity or any other opportunity, please forward your CV to Nelson Anthony (-).

If you would like to find out about the latest Jobs and Projects we are involved in then do follow us on LinkedIn:

PES International operates as an equal opportunity employer. No terminology in this advert is intended to discriminate on the grounds of age, race, religion, sexual orientation or any other factors with no bearing to employment skills and we confirm that we are happy to accept applications from persons of any background for this role.

Overview
PES is an international services company providing Project Management, Construction Management, Commissioning & Qualification and Automation services to our clients in the pharmaceutical, nutritional and related sectors.
With offices across Europe, Asia and US, our core focus is on consistently delivering high-quality outcomes for our multinational clients.
This focus, and our people's experience in delivering consistent quality results for our clients over the past 20 years has been key to our success to date.
We are currently looking for
Validation Engineers
to join us on a permanent role to help us deliver various projects in the Life Sciences Industry.
Responsibilities
Looking for candidates with 0-3 years validation/CQV experience.
Using the process automation system for the commissioning and validation of process equipment.
Protocol Development (IQ,OQ, PQ) / protocol review for process equipment.
Interface with client personnel and with outside vendors when necessary while performing the above.
Managing validation projects.
Individual will manage all facets of assigned validation projects while maintaining strong communication with client representatives on project status and assistance needed.
We are currently looking for candidates in Singapore.
How to apply
If you'd like to find out about this opportunity or any other opportunity, please forward your CV to Nelson Anthony ( ).
If you would like to find out about the latest Jobs and Projects we are involved in then do follow us on LinkedIn:
Equal Opportunity
PES International operates as an equal opportunity employer. No terminology in this advert is intended to discriminate on the grounds of age, race, religion, sexual orientation or any other factors with no bearing to employment skills and we confirm that we are happy to accept applications from persons of any background for this role.
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Job Responsibilities
Build and maintain strong customer relationships by delivering responsive and high-quality service support.
Perform installation, commissioning, calibration, maintenance, troubleshooting, and repair of scientific and analytical analyzer systems at customer sites.
Provide technical training to end-users and distributors to ensure effective equipment usage and maintenance.
Address and resolve service-related concerns by liaising directly with customers on issues involving instruments (Spectroscopy, Particle Size Analyzers, ICP systems, and XRF.)
Collaborate closely with internal sales and regional technical teams to support customer needs and coordinate service delivery.
Prepare quotations for service jobs and spare parts based on customer inquiries.
Identify potential leads for preventive maintenance contracts during service visits.
Job Requirements
Minimum Diploma in (Mechanical/Electronics/Electrical/Chemical Engineering) or equivalent qualification.
Preferably 1–2 years of hands-on experience in servicing scientific or analytical instrumentation.
Strong customer service orientation with a proactive and positive attitude.
Capable of working independently with good planning, time management, and problem-solving skills.
Self-driven, responsible, and adaptable to new challenges.
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

EA License No: 13C6305
Reg. No.: R (NG KHO YIN)
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.
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