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Showing 236 Industrial Electrician jobs in Singapore
Job Description
Our client, a well-established market leader within the industrial sector, is seeking an experienced Credit Control Manager to oversee and strengthen its credit management function. Reporting to the Financial Controller, this role will play a critical part in protecting the company's financial interests through effective credit risk assessment, collections management and receivables optimisation.
The successful candidate will be responsible for evaluating credit applications, conducting credit checks on both new and existing customers and assessing customer creditworthiness through detailed business and financial analysis. The role will also involve working closely with credit insurers to ensure appropriate credit limits are in place, preparing internal credit approval recommendations and regularly reviewing customer portfolios to proactively manage credit exposure and minimise bad debt risks.
As a key business partner, the Credit Control Manager will collaborate closely with commercial teams and internal stakeholders to resolve customer disputes, negotiate payment arrangements, and drive timely collections. The incumbent will be expected to identify and escalate high-risk accounts, recommend credit holds where necessary and support legal recovery actions for problematic customers while balancing commercial considerations and business growth objectives.
The role also carries leadership responsibilities, including overseeing and developing the credit control team, ensuring compliance with established policies and procedures and providing management with timely updates on emerging credit risks and mitigation strategies. A strong understanding of credit control practices, contract and business law, market credit conditions and risk management principles will be essential for success in this position.
The ideal candidate will possess a Degree or Diploma in Business, Commerce, Finance, or a related discipline, coupled with at least 8 years of relevant credit control or credit risk management experience, including several years in a managerial capacity. Strong analytical, negotiation, stakeholder management and communication skills are highly valued, as is the ability to lead teams and influence business decisions in a dynamic environment.
Singapore Employment Agency License No:16S8069
Consultant Registration No: R
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Job Description
Key Job Accountabilities :
• Lead and manage semiconductor backend manufacturing operations across Backgrind, Laser Mark, , Laser groove, Wafer Saw, AOI, and Tape & Reel processes to achieve safety, quality, delivery, cost, and productivity targets.
• Drive operational excellence through continuous improvement initiatives focused on yield enhancement, cycle time reduction, equipment utilization, and cost optimization.
• Lead multiple production shifts through supervisors and engineers, ensuring effective manpower planning, workforce development, and operational discipline.
• Manage customer escalations, production risks, and quality excursions, ensuring timely containment, root cause analysis, and corrective actions.
• Partner with Process, Equipment, Quality, Planning, and Maintenance teams to resolve complex manufacturing issues and improve process robustness.
• Monitor and drive key manufacturing KPIs including OEE, yield, UPH, cycle time, on-time delivery, scrap, and labor productivity.
• Support New Product Introduction (NPI), process transfers, and manufacturing readiness activities to meet customer and business requirements.
• Champion Lean Manufacturing, Six Sigma, automation, and Industry 4.0 initiatives to improve factory performance and scalability.
• Ensure compliance with quality systems, customer requirements, EHS standards, and audit expectations.
• Develop and execute manufacturing strategies, organizational capability, and succession plans to support long-term business growth.
Required Experience and Qualifications:
- Minimum Degree in any disciplines.
- Preferably 10 years experience in semiconductor industry.
- Experience managing manufacturing operations for minimum of 5 years
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Job Description
About the Company
Senior Manager, Manufacturing Operations
About the Role
The Senior Manager, Manufacturing Operations is responsible for providing strategic leadership and oversight of end-to-end manufacturing operations to achieve business objectives, production commitments, and customer expectations. This role drives operational excellence, organizational capability building, and continuous improvement initiatives while ensuring the highest standards of quality, productivity, regulatory compliance, and cost efficiency.
Responsibilities
- Lead and transform the manufacturing organization by developing high-performing teams and fostering a culture of accountability, continuous improvement, and operational excellence.
- Develop and execute manufacturing strategies aligned with business objectives, customer requirements, and long-term growth plans.
- Provide leadership and direction to cross-functional teams across manufacturing, engineering, quality, supply chain, and planning functions to optimize operational performance.
- Oversee all manufacturing activities, ensuring compliance with regulatory requirements, industry standards, quality management systems, and environmental, health, and safety regulations.
- Drive the execution of production strategies to achieve delivery targets, capacity optimization, productivity improvements, and cost competitiveness.
- Lead manufacturing transformation initiatives, including Lean, Six Sigma, automation, digitalization, and process optimization programs.
- Own manufacturing budgets, operating expenditure, and capital investment planning to ensure effective resource allocation and return on investment.
- Partner with supply chain and planning teams on production scheduling, inventory optimization, material flow management, and demand planning.
- Establish operational metrics and governance processes to monitor performance related to safety, quality, output, yield, delivery, and cost.
- Identify and mitigate operational risks while driving corrective and preventive actions to improve overall business performance.
- Build organizational capability through talent development, succession planning, employee engagement, and leadership coaching.
Qualifications
- Bachelor's Degree in Engineering, Manufacturing, Operations Management, or a related discipline. A Master's degree or professional certifications in Lean, Six Sigma, or Operations Excellence is advantageous.
- Minimum 12–15 years of manufacturing operations experience, including at least 7 years in senior leadership roles managing large-scale manufacturing operations and cross-functional teams.
- Proven track record of leading manufacturing operations within highly regulated industries such as medical devices, life sciences, pharmaceuticals, precision engineering, semiconductor, or advanced manufacturing environments.
- Demonstrated success in driving manufacturing transformation, operational excellence initiatives, and large-scale continuous improvement programs.
- Strong expertise in production planning, capacity management, supply chain integration, budgeting, and capital expenditure management.
- In-depth knowledge of quality management systems, regulatory compliance, and international standards, including ISO and environmental, health, and safety requirements.
- Strong commercial acumen with experience balancing operational performance, customer satisfaction, and business profitability.
- Exceptional stakeholder management, communication, and influencing skills, with the ability to engage senior leadership and drive organizational alignment.
- Proven ability to lead, inspire, and develop high-performing teams in complex and fast-paced manufacturing environments.
Required Skills
- Leadership and team development
- Operational excellence and continuous improvement
- Manufacturing strategy execution
- Cross-functional collaboration
- Regulatory compliance and quality management
Preferred Skills
- Lean and Six Sigma methodologies
- Digitalization and automation in manufacturing
- Advanced manufacturing technologies
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Job Description
Applied Materials is a global leader in materials engineering solutions used to produce virtually every new chip and advanced display in the world. We design, build and service cutting-edge equipment that helps our customers manufacture display and semiconductor chips - the brains of devices we use every day. As the foundation of the global electronics industry, Applied enables the exciting technologies that literally connect our world - like AI and IoT. If you want to push the boundaries of materials science and engineering to create next generation technology, join us to deliver material innovation that changes the world.
**What We Offer**
Location:
Singapore,SGP
You'll benefit from a supportive work culture that encourages you to learn, develop, and grow your career as you take on challenges and drive innovative solutions for our customers. We empower our team to push the boundaries of what is possible-while learning every day in a supportive leading global company. Visit our Careers website to learn more.
At Applied Materials, we care about the health and wellbeing of our employees. We're committed to providing programs and support that encourage personal and professional growth and care for you at work, at home, or wherever you may go. Learn more about our benefits ( .
As a Manufacturing Engineer, you are responsible for developing and maintaining methods, operating sequences, and processes in the fabrication of parts, components, subassemblies, and final assemblies. You'll work closely with other engineering functions to coordinate the release of product improvements and new products, and you'll use engineering principles to estimate and reduce manufacturing costs, improve product quality, determine time standards, and make recommendations for tooling and process requirements. Your expertise in lean principles, automation, and continuous improvement will be instrumental in driving operational excellence and achieving higher levels of productivity and cost-effectiveness. You'll develop and use test procedures, evaluate test results, and assess work methods, procedures, and policies to identify root cause issues and solutions that ensure operational success.
**Role Responsibilities:**
+ Develop and maintain all methods, operating sequences, and processes in the fabrication of parts, components, subassemblies, and final assemblies
+ Work with other engineering functions to coordinate the release of product improvements and new products, and manage manufacturing engineering projects as needed
+ Lead team in using design for excellence (DFx) principles to estimate and reduce manufacturing and/or product costs, and to improve product quality
+ Determine time standards and make recommendations for tooling and process requirements
+ Develop and use test procedures, evaluate test results, and evaluate work methods, procedures, and policies
+ Determine root causes and corrective actions for issues that arise during assembly or system testing; perform Process Failure Mode & Effects Analysis; and provide reports as needed
+ Mentor and train junior level engineers
**Minimum Qualifications:**
+ Bachelor's degree
+ 4-7 years of experience
+ Demonstrated conceptual knowledge and technical experience for everyday problem-solving on the job
**Preferred Qualifications:**
+ Solid interpersonal skills-including the ability to clearly explain difficult or sensitive information, and the ability to build consensus
**Physical Requirements:**
This position may require standing for extended periods of time, walking, working in tight spaces, bending, squatting, twisting, kneeling, reaching, lifting, the ability to distinguish between colors, the ability to work in an environment with noise that may be difficult for some individuals with sensitivity to noise, and the use of hand and power tools. Additionally, because this position also may involve working in a clean room, the use of appropriate Personal Protective Equipment such as coveralls, hoods, booties, safety glasses, gloves, respirators, chemical aprons, and face shields may be required.
**Additional Information**
**Time Type:**
Full time
**Employee Type:**
Assignee / Regular
**Travel:**
Yes, 20% of the Time
**Relocation Eligible:**
No
Applied Materials is an Equal Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, national origin, citizenship, ancestry, religion, creed, sex, sexual orientation, gender identity, age, disability, veteran or military status, or any other basis prohibited by law.
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Job Description
We are seeking a Quality Technician to support our expanding manufacturing site in Singapore. This role is responsible for incoming quality and sampling inspections for critical assemblies, ensuring compliance with quality standards and specifications.
Key responsibilities:
- Operate lasers and with good testing/reliability testing/incoming receiving inspection testing skill
- Conduct testing of optics & optics alignment
- Troubleshoot laser/optics and report unsolvable issues to respective engineers
- Raise Quality notifications (QNs) for laser test failures & logistics support/transactions in SAP
- Assist engineers on the routine manufacturing engineering matters (like BOM validation, engineering evaluations, data collection etc.)
- Analyze data and report problems, to complete accurate, IRI reports, and to communicate technical issues to other technical staff.
- Install and align optical, mechanical and optical sub-assemblies into systems using precision instruments
- Apply continuous improvement concepts and techniques in daily work activities.
- Performs other duties as assigned by supervisor based on business needs.
Requirements:
- Minimum Higher NITEC or Diploma in Engineering (Electrical/Electronic) or equivalent
- 4+ years of experience in incoming inspection, laser manufacturing or testing.
- Familiarity with optics metrology and laser testing will be an advantage.
- Strong attention to detail and good documentation skills.
- Able to read and interpret technical drawings, specifications and manufacturing documents.
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Job Description
Job Description
Directs the development and implementation of activities in production area(s) to meet production goals, quality, and cost objectives. Prioritizes production schedules based on product introduction, equipment efficiency, and materials supply. Plans and administers procedures and budgets. Makes budgetary recommendations and at higher levels, controls capital expenditures and direct/indirect labor. Develops schedules and manpower requirements for assigned areas. Selects, develops, and evaluates personnel to ensure the efficient operation of the function
Responsibilities
- Manage activities of several Production Cells with focus on Production Operations Excellence, Safety, Resources Planning, Productivity, Yield, 5S, OTD and Product Quality.
- Work with supervisors to analyze and correct problems and to ensure budgets, schedules, and performance requirements are met
- Provide technical leadership in the manufacturing processes and techniques and maintain all WIP and shop-floor items accordingly with control of MR issuance
- Estimate manpower needs and assign work to meet objectives according to push-pull.
- Manage staffing, training and performance evaluations to develop and improve staff skill set and career pathing with a regular review cadence.
- Establish operational objectives and plans weekly production schedules. Meet with supervisors to analyze and correct problems and to ensure budgets, schedules, and performance requirements are met.
- Address and remedy Quality and Workmanship issues with a ‘Poka-Yoke ‘ or Engineering approach in most instances.
- Plan and establish production capacity to cater to customer demand ramp.
Continuous Improvement and General Requisites
- Drive and participate in mining Continuous Improvement programs within production cells and Plant wide to reduce waste, reduce cost, reduce errors and improve productivity as well as Safety and Quality.
- Thorough knowledge of production and process principles and manufacturing operations
- Solid knowledge of the company’s policies, practices and procedures with the ability to work within parameters and excel in a cross-functional work environment.
Requirements
- Degree in Engineering, Manufacturing Technology
- Minimum of 8 years manufacturing experience at management level
- Has the maturity to make sound decisions independently and be resourceful in day-to-day issues
- Must have Manufacturing experience from a Semiconductor industry leading a team of manufacturing staff from all levels for > 180 HC.
- Excellent time management, organizational, and problem-solving skills
- Ability to exercise good discretion and exercise independent judgment
- Proven people skills with the ability to evaluate, coach, and motivate employees
- Strong verbal /written communication and confident presentation skills
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Manufacturing Biotechnologist
Posted 2 days ago
Job Viewed
Job Description
The Opportunity
Esco Lifesciences Group is Singapore’s most globalized life sciences company, with annual revenues close to SGD 200M and global operations in over 42 locations and 26 direct countries across North America, Europe, Asia, Oceania.
Esco Aster Pte Ltd is an affiliate of Esco Lifesciences Group and was first incorporated in 2017.
Esco Aster is a contract research development and manufacturing organization founded and deeply rooted by scientists enabling fellow scientists to translate their bench work into commercially available products at affordable prices.
Our scientific work is in emerging and frontier biology utilizing cells as a final product or deriving products from cells which often we use cells as the factory to derive our target product.
Our first commercial breakthrough success is Esco Aster is commercially first in class being first in the world to be certified for cultivated/cell-based meat to FSSC 22000 and by a competent food regulatory body.
We are first in the region to operate an end-to-end integrated full cell line creation/immortalization or engineered cell line, cell culture process development, analytical development for stem cells and exosomes with full cGMP Capabilities from Drug Substance and small-scale fill & finish for final Cell Therapy Product.
The work we do creates a remarkable and lasting impact on our world. We offer you an opportunity to be part of this exciting journey to own your career and firsthand exposure to new emerging modalities supporting translational sciences.
Join us as we redefine BioSolutions for One World and One Health for the current and future generations to come.
Esco Aster.
One World Biosolutions for One Health.
Who we’re looking for
Physical / Mental Requirements / Work Environment:
- Strong leadership and communication skills.
- Ability to stay focused under pressure and adapt proactively.
- Critical thinker with a systematic and meticulous approach.
- Curious and self-motivated to stay updated on cell/gene therapy and emerging technologies.
- Committed to safety, quality, compliance, and timely delivery.
- Cleanroom and GMP manufacturing settings.
- Requires standing for long periods, working with sterile systems, and wearing full gowning/PPE.
- May engage in overtime during campaign activities or urgent troubleshooting.
The Scope
To support the successful technology transfer, manufacturing execution, and commercial readiness of cell and gene therapy products in a cGMP environment, ensuring compliance, efficiency, and delivery excellence throughout the product lifecycle.
Primary work location: Ayer Rajah Crescent, Singapore
Job Responsibilities
- Collaborate with internal/external stakeholders including QA, QC, MSAT, and commercial teams.
- Serve as Manufacturing Subject Matter Expert (SME) during audits, inspections, and due diligence.
- Involve in technology transfers (internal and external) and commissioning, qualification (C&Q) activities.
- Involve in Process Performance Qualification (PPQ), Aseptic Process Simulations (APS), and engineering/pilot runs.
- Support in cell culture, purification, and fill-finish operations in a single-use, aseptic, cGMP facility.
- Help in Ensuring readiness of raw materials, equipment, and team for autologous/ allogeneic campaigns.
- Ensure accurate and timely data entry in digital records, maintaining compliance with Good Documentation Practices (GDP).
- Author, review, and manage cGMP documentation: SOPs, batch records, risk assessments, protocols, etc.
- Support with manufacturing change control, deviation investigations and implement CAPAs.
- Support the implementation of electronic batch records.
- Undertake other tasks as assigned by the management based on project needs.
Requirements
- Minimum Bachelor’s Degree in Biotechnology related disciplines, Chemical Engineering, Pharmaceutical Science or relevant discipline with 2 years or more experience in a cGMP/aseptic environment in biologics or cell and gene therapy.
- Minimum of 2-4 years in cGMP Biologics or cell and gene therapy manufacturing with relevant industry knowledge, hands on equipment experience and technical expertise. Upstream Manufacturing Process.
- Experience in Downstream and Upstream Manufacturing Process and/or Process Support services.
- Strong knowledge of cGMP practices and global regulatory requirements such as USFDA GMP, EU GMP, HSA GMP and PIC/S GMP.
- Proficient in MS Office Suite (Microsoft Word, PowerPoint, Excel).
- Able to work independently and task oriented in a dynamic environment.
- Strong team player with a strong set of interpersonal skills.
- Excellent written and verbal communication skills.
- Experience in working in cell and gene therapy manufacturing is an added advantage.
Apply now by submitting a Cover Letter and CV to .
Only shortlisted candidates will be contacted.
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Job Description
Our client is a recognized Global Precision Equipment Design & Manufacturing business. They are market leaders in the innovative development with high quality manufacturing standards for a variety of customized innovative and complex Manufacturing Equipment Solutions globally. The company has a significant presence in Asia in terms of its reputable market position in developing best-in-class manufacturing and operations excellence capabilities and takes pride in ensuring optimized regional activities to achieve maximized customer satisfaction.
They are currently on an active look out for a suitable candidate as a Senior Manager, Manufacturing (Singapore), who is the critical point of contact in terms of ensuring smooth designing and implementation of improvised Production Management processes for Singapore Manufacturing activities and beyond.
RESPONSIBILITIES:
Reporting to the Singapore Site GM, and this position will be focusing on the below:
- Directly lead a large team of managing end to end Product Manufacturing Management to make happen successful optimization of utilization of manufacturing equipment, systems, and resources to meet changing production demands.
- Subject matter expert to spearhead the strategic manufacturing process improvement by working closely with Quality and Engineering teams onsite.
- Deep dive into critical production control pain points to optimize Production Scheduling and maximizing output for Singapore manufacturing activities and beyond.
- Strategize and develop improved processes by means of conducting strategic Root Cause Analysis by means of introducing an efficient Operations Excellence methodology.
REQUIREMENTS:
Candidate Profile
Singapore • Permanent
- Bachelor’s Degree with at least 8-10 years of relevant experience in end-to-end Manufacturing or related International Engineering and/or Business Management experiences in a complex and high mix low volume Precision Manufacturing environment.
- Proven track record in acquired solution-oriented mind set to deal with complex and matrix organizational framework.
- Excellent hands-on experience and knowledge in driving Manufacturing Excellence.
- Excellent interpersonal communication skills to relay and/or drive process improvements across a global organization to regional/ global stakeholders involved.
- Good understanding of SAP and equivalent ERP system is highly preferred
Please contact Hui Ting at for a confidential discussion
EA License no: 16S8066 | Reg no.: R
Only successful candidates will be notified.
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Build Manufacturing Engineer (4pm - 1.30am)
Posted 19 days ago
Job Viewed
Job Description
Applied Materials is a global leader in materials engineering solutions used to produce virtually every new chip and advanced display in the world. We design, build and service cutting-edge equipment that helps our customers manufacture display and semiconductor chips - the brains of devices we use every day. As the foundation of the global electronics industry, Applied enables the exciting technologies that literally connect our world - like AI and IoT. If you want to push the boundaries of materials science and engineering to create next generation technology, join us to deliver material innovation that changes the world.
**What We Offer**
Location:
Singapore,SGP
You'll benefit from a supportive work culture that encourages you to learn, develop, and grow your career as you take on challenges and drive innovative solutions for our customers. We empower our team to push the boundaries of what is possible-while learning every day in a supportive leading global company. Visit our Careers website to learn more.
At Applied Materials, we care about the health and wellbeing of our employees. We're committed to providing programs and support that encourage personal and professional growth and care for you at work, at home, or wherever you may go. Learn more about our benefits ( .
As a Manufacturing Engineer, you are responsible for developing and maintaining methods, operating sequences, and processes in the fabrication of parts, components, subassemblies, and final assemblies. You'll work closely with other engineering functions to coordinate the release of product improvements and new products, and you'll use engineering principles to estimate and reduce manufacturing costs, improve product quality, determine time standards, and make recommendations for tooling and process requirements. Your expertise in lean principles, automation, and continuous improvement will be instrumental in driving operational excellence and achieving higher levels of productivity and cost-effectiveness. You'll develop and use test procedures, evaluate test results, and assess work methods, procedures, and policies to identify root cause issues and solutions that ensure operational success.
Applied Materials South East Asia is a strategic hub for Applied Materials, consisting of diverse business activities across manufacturing, R&D, corporate functions and field services in Singapore, Malaysia and the Philippines. Singapore serves as the regional headquarters for Applied Materials. Since its establishment in 1991, the Applied Materials Singapore Operations Center has become our largest factory outside the United States. Singapore manufacturing accounts for around 50% of global semiconductor equipment output.
As a Build Manufacturing Engineer, you need to rise to the challenge of building systems that meet our customers' needs for highly specialized solutions. The assembled systems may look similar, but the value comes in the sophisticated ways we seamlessly incorporate their many unique requirements.
**Key Responsibilities:**
+ Develops, implements, and maintains methods, operation sequence and processes in the fabrication of parts, components, sub-assemblies and final assemblies.
+ Interfaces with other engineering functions to coordinate the release of product improvements and/or new products. Launches, releases, approves and implements or issues engineering change requests as required to support design engineering and Operations with new and existing products.
+ Estimates manufacturing costs, determines time standards and makes recommendations for tooling and process requirements. Uses DFx principles to reduce manufacturing and/or product costs, and improve delivered product quality.
+ Develops and uses test procedures, including assisting with the definition of test specifications with design / software engineering. May work with test engineering on the design and development of text fixtures. May assist in the coordination of test fixture sourcing activities.
+ Gathers operational and test data and evaluates results; may takes corrective/continuous improvement actions.
+ Evaluates work methods, procedures and policies. Participates in the development and maintenance of new and existing business processes; updates as necessary to ensure current practices are documented.
+ Determines root cause and corrective action analysis for issues that arise during assembly and/or test of systems; provides failure analysis report as required.
+ Performs Process Failure Mode, Effects and Criticality Analysis when working with New Product Development.
**Requirements:**
+ Bachelor Degree in Engineering or equivalent
+ More than 3 years of relevant experiences in semiconductor or manufacturing industry
+ Ability to commit permanent second shift (4pm - 1.30am). Transport will be provided.
+ Ability to work with any levels of stakeholders globally
+ Ability to attend meetings on different time zones when necessary
+ Meticulous, resourceful and proactive
**Work Location:**
+ Upper Changi
**Additional Information**
**Time Type:**
Full time
**Employee Type:**
Assignee / Regular
**Travel:**
Yes, 10% of the Time
**Relocation Eligible:**
No
Applied Materials is an Equal Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, national origin, citizenship, ancestry, religion, creed, sex, sexual orientation, gender identity, age, disability, veteran or military status, or any other basis prohibited by law.
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Manufacturing Lead
Posted 14 days ago
Job Viewed
Job Description
Manufacturing Lead
The Opportunity
Esco Lifesciences Group is Singapore’s most globalized life sciences company, with annual revenues close to SGD 200M and global operations in over 42 locations and 26 direct countries across North America, Europe, Asia, Oceania.
Esco Aster Pte Ltd is an affiliate of Esco Lifesciences Group and was first incorporated in 2017.
Esco Aster is a contract research development and manufacturing organization founded and deeply rooted by scientists enabling fellow scientists to translate their bench work into commercially available products at affordable prices.
Our scientific work is in emerging and frontier biology utilizing cells as a final product or deriving products from cells which often we use cells as the factory to derive our target product.
Our first commercial breakthrough success is Esco Aster is commercially first in class being first in the world to be certified for cultivated/cell-based meat to FSSC 22000 and by a competent food regulatory body.
We are first in the region to operate an end-to-end integrated full cell line creation/immortalization or engineered cell line, cell culture process development, analytical development for stem cells and exosomes with full cGMP Capabilities from Drug Substance and small-scale fill & finish for final Cell Therapy Product.
The work we do creates a remarkable and lasting impact on our world. We offer you an opportunity to be part of this exciting journey to own your career and firsthand exposure to new emerging modalities supporting translational sciences.
Join us as we redefine BioSolutions for One World and One Health for the current and future generations to come.
Esco Aster.
One World Biosolutions for One Health.
Who we’re looking for
Physical / Mental Requirements / Work Environment:
- Strong leadership and communication skills.
- Ability to stay focused under pressure and adapt proactively.
- Critical thinker with a systematic and meticulous approach.
- Curious and self-motivated to stay updated on cell/gene therapy and emerging technologies.
- Committed to safety, quality, compliance, and timely delivery.
- Cleanroom and GMP manufacturing settings.
- Requires standing for long periods, working with sterile systems, and wearing full gowning/PPE.
- May engage in overtime during campaign activities or urgent troubleshooting.
The Scope
To lead and manage the successful technology transfer, manufacturing execution, and commercial readiness of cell and gene therapy products in a cGMP environment, ensuring compliance, efficiency, and delivery excellence throughout the product lifecycle.
Primary work location: Ayer Rajah Crescent, Singapore
Job Responsibilities
- Lead cross-functional biotechnicians and act as the bridge between process development and manufacturing.
- Collaborate with internal/external stakeholders including QA, QC, MSAT, and commercial teams.
- Serve as Manufacturing Subject Matter Expert (SME) during audits, inspections, and due diligence.
- Manage end-to-end technology transfers (internal and external).
- Involve in commissioning, qualification (C&Q) activities.
- Oversee execution of Process Performance Qualification (PPQ), Aseptic Process Simulations (APS), and engineering/pilot runs.
- Oversee cell culture, purification, and fill-finish operations in a single-use, aseptic, cGMP facility.
- Ensure readiness of raw materials, equipment, and team for autologous/allogeneic campaigns.
- Monitor, document, and troubleshoot manufacturing activities, ensuring compliance with SOPs and regulatory requirements.
- Author, review, and manage cGMP documentation: SOPs, batch records, risk assessments, protocols, etc.
- Lead manufacturing change control, deviation investigations and implement CAPAs.
- Lead the implementation of electronic batch records.
- Potentially leading a small team.
- Undertake other tasks as assigned by the management based on project needs.
Requirements
- Minimum Bachelor’s Degree in Biotechnology related disciplines, Chemical Engineering, Pharmaceutical Science or relevant discipline with 2 years or more experience in a cGMP/aseptic environment in biologics or cell and gene therapy.
- Minimum of 4-6 years in cGMP Biologics or cell and gene therapy manufacturing with relevant industry knowledge, hands on equipment experience and technical expertise.
- Strong knowledge of cGMP practices and global regulatory requirements such as USFDA GMP, EU GMP, HSA GMP and PIC/S GMP.
- In-depth knowledge of the drug development process and commercialization pathways.
- Proficient in MS Office Suite (Microsoft Word, PowerPoint, Excel).
- Able to work independently and task oriented in a dynamic environment.
- Strong team player with a strong set of interpersonal skills.
- Excellent written and verbal communication skills.
- Experience in bringing cell and gene therapy products through clinical development to market is an added advantage.
- Proven track record in regulatory strategy and interactions is an added advantage.
- Proficient in MS Office Suite (Microsoft Word, PowerPoint, Excel).
- Able to work independently and task oriented in a dynamic environment.
- Strong team player with a strong set of interpersonal skills.
- Excellent written and verbal communication skills.
Apply now by submitting a Cover Letter and CV to .
Only shortlisted candidates will be contacted.
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