156 Laboratory Technicians jobs in 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

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.

Due to our constant growth, we are looking for a Senior CQV Engineer with strong experience in laboratory equipment and lab decommissioning activities to support our projects in Singapore.

You will be responsible for:

• Leading commissioning, qualification, and decommissioning activities specifically related to laboratory equipment and facilities.

• Preparing, reviewing, and executing CQV protocols and reports for laboratory instruments.

• Coordinating and executing lab decommissioning activities, ensuring safe removal, regulatory compliance, and documentation traceability.

• Collaborating with engineering, QA, operations, and laboratory teams to ensure seamless execution of lab-focused CQV activities.

• Managing timelines and deliverables to align with overall project schedules.

• Supporting audit readiness by ensuring complete and compliant documentation of all CQV and decommissioning activities.

About you:

• 5–10 years of experience in commissioning, qualification, and decommissioning within the pharmaceutical/biotech industries.

• Proven hands-on experience with laboratory equipment (e.g., incubators, centrifuges, refrigerators, freezers, balances, environmental chambers).

• Direct experience in lab decommissioning projects, including documentation and compliance with GMP and regulatory guidelines.

• Strong knowledge of GMP, FDA, EMA, and other international standards.

• Excellent organizational, coordination, and problem-solving skills.

• Fluent in English, both written and spoken.

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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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
Qualifications
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.
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 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.
Additional Information
Location: Johor Bahru, Johore, Malaysia
Seniority level: Associate
Employment type: Full-time
Job function: Engineering and Quality Assurance
Industries: Pharmaceutical Manufacturing
#J-18808-Ljbffr

Overview
QC Specialist – Analytical Methods, GxP Lab Equipment & LIMS (Pharma)
Salary Up to $7,000 depending on experience
Location : Tuas
Industry : Pharmaceutical
Our client is a global leader in the pharmaceutical industry, producing and delivering over 4 billion units of medicines and vaccines each year—making a real difference in getting life-saving treatments to those who need them most. They are driving the future of healthcare with state-of-the-art facilities, AI-powered smart factories, and cutting-edge automation, ensuring medicines reach patients faster, safer, and more sustainably.
Responsibilities
Represent the site in global Communities of Practice (CoPs) and Centers of Excellence (CoEs) for QC processes and ensure effective local communication.
Maintain the site Validation Master Plan and procedures related to Analytical Lifecycle Management (ALCM) and Continued Process Verification (CPV) for GxP laboratory equipment.
Oversee lifecycle management, qualification, and maintenance of QC lab equipment, ensuring compliance with regulatory and quality standards.
Lead and support analytical method lifecycle activities including method reviews, trending, data evaluation, and compendial compliance.
Drive implementation and maintenance of QC digital solutions (e.g., LIMS), including data integrity and end-user management.
Support and investigate quality control events, deviations, and CAPAs within the QC scope.
Coordinate documentation, review, and approval of qualification deliverables (e.g., risk assessments, protocols, reports).
Provide technical leadership in analytical validation, method transfers, and lab projects.
Act as SME for laboratory computerized systems and provide system administrator support.
Support regulatory inspections and customer audits by presenting relevant documentation and records.
Ensure safe laboratory operations and compliance with HSE and cGMP requirements.
Deputize for QC Manager as required.
Qualifications
Ideally 5 years of experience in quality control within pharmaceutical with knowledge of Good Manufacturing Practices (GMP), regulatory requirements and expertise on lab instruments.
Excellent interpersonal relationships to establish the partnerships necessary for the development of the Quality culture.
Knowledge of regulations and standards of the pharmaceutical industry, Global Quality policies and Data Integrity Requirements.
Knowledge of the quality systems and associated technologies.
Ability to analyze complex data and laboratory results to make informed decisions and identify areas for improvement.
Keen attention to detail to ensure accuracy in testing, reporting, and compliance with regulatory requirements.
Proficiency in identifying issues and implementing effective solutions to resolve quality control problems.
Good understanding of good laboratory practices, good documentation practice and data integrity requirements.
Experienced in analytical method continuous monitoring requirements.
Lim Pey Chyi -
Recruitment Consultant (R )
Manpower Staffing Services (S) Pte Ltd
EA Licence: 02C3423
#J-18808-Ljbffr

QC Specialist – Analytical Methods, GxP Lab Equipment & LIMS (Pharma)

Salary Up to $7,000 depending on experience

Location : Tuas

Industry : Pharmaceutical

Our client is a global leader in the pharmaceutical industry, producing and delivering over 4 billion units of medicines and vaccines each year—making a real difference in getting life-saving treatments to those who need them most. They are driving the future of healthcare with state-of-the-art facilities, AI-powered smart factories, and cutting-edge automation, ensuring medicines reach patients faster, safer, and more sustainably.

Responsibilities :

• Represent the site in global Communities of Practice (CoPs) and Centers of Excellence (CoEs) for QC processes and ensure effective local communication.
• Maintain the site Validation Master Plan and procedures related to Analytical Lifecycle Management (ALCM) and Continued Process Verification (CPV) for GxP laboratory equipment.
• Oversee lifecycle management, qualification, and maintenance of QC lab equipment, ensuring compliance with regulatory and quality standards.
• Lead and support analytical method lifecycle activities including method reviews, trending, data evaluation, and compendial compliance.
• Drive implementation and maintenance of QC digital solutions (e.g., LIMS), including data integrity and end-user management.
• Support and investigate quality control events, deviations, and CAPAs within the QC scope.
• Coordinate documentation, review, and approval of qualification deliverables (e.g., risk assessments, protocols, reports).
• Provide technical leadership in analytical validation, method transfers, and lab projects.
• Act as SME for laboratory computerized systems and provide system administrator support.
• Support regulatory inspections and customer audits by presenting relevant documentation and records.
• Ensure safe laboratory operations and compliance with HSE and cGMP requirements.
• Deputize for QC Manager as required.

Requirements

• Ideally 5 years of experience in quality control within pharmaceutical with knowledge of Good Manufacturing Practices (GMP), regulatory requirements and expertise on lab instruments.
• Excellent interpersonal relationships to establish the partnerships necessary for the development of the Quality culture.
• Knowledge of regulations and standards of the pharmaceutical industry, Global Quality policies and Data Integrity Requirements.
• Knowledge of the quality systems and associated technologies.
• Ability to analyze complex data and laboratory results to make informed decisions and identify areas for improvement.
• Keen attention to detail to ensure accuracy in testing, reporting, and compliance with regulatory requirements.
• Proficiency in identifying issues and implementing effective solutions to resolve quality control problems.
• Good understanding of good laboratory practices, good documentation practice and data integrity requirements.
• Experienced in analytical method continuous monitoring requirements.

Lim Pey Chyi -

Recruitment Consultant (R )

Manpower Staffing Services (S) Pte Ltd

EA Licence: 02C3423