773 Applied Materials jobs in Singapore

Overview

We are seeking a highly skilled and detail-oriented Manufacturing Process Engineer to join our team in the precision engineering sector. The Manufacturing Process Engineer will be responsible for developing, implementing, and improving manufacturing processes to achieve the highest standards of quality and efficiency. This role requires a deep understanding of engineering principles, advanced manufacturing techniques, and a strong commitment to innovation and continuous improvement.

Duties and Responsibilities

Process Development and Implementation

• Design and develop manufacturing processes for new products and optimize existing processes to improve quality and efficiency.
• Conduct feasibility studies and cost analyses for manufacturing projects.
• Collaborate with design, production, and quality teams to ensure seamless integration of new processes.
• Create detailed process documentation, including work instructions, process flow diagrams, and standard operating procedures.
• Transfer process knowledge to production teams.

Continuous Improvement

• Identify opportunities for process improvements and implement lean manufacturing principles to reduce waste and increase productivity.
• Analyze production data to identify trends and areas for improvement.
• Lead cross-functional teams in problem-solving and root cause analysis activities.
• Develop and implement corrective and preventive actions to address process deficiencies.

Quality Assurance

• Ensure that all manufacturing processes comply with industry standards and regulatory requirements.
• Work closely with the quality team to develop and implement quality control plans.
• Participate in internal and external audits and address any findings related to manufacturing processes.

Technical Support

• Provide technical support to production teams to resolve manufacturing issues and improve process performance.
• Train and mentor production staff on new processes and best practices.
• Collaborate with equipment vendors and suppliers to identify and implement new technologies and equipment.
• Maintain up-to-date knowledge of industry trends, technologies, and best practices.

Position Requirements

• Education Requirements: Bachelor’s Degree in Manufacturing Engineering, Mechanical Engineering, or related field.
• Experience Level Requirements : Minimum of 5 years of experience in manufacturing engineering, preferably in the precision engineering sector.

Skills Desired:

• Strong knowledge of manufacturing processes, materials, and equipment used in precision engineering.
• Experience with CAD/CAM software, ideally SolidWorks, MasterCam and other engineering tools.
• Knowledge of technical drawings and BOM.
• Proven ability to lead process improvement initiatives and implement lean manufacturing principles.
• Excellent problem-solving skills and attention to detail.
• Strong communication and interpersonal skills, with the ability to work effectively in cross-functional teams.
• Able to work under pressure with minimum supervision
• Knowledge of industry standards and regulatory requirements applicable to precision engineering.

Overview

We are seeking a highly skilled and detail-oriented Manufacturing Process Engineer to join our team in the precision engineering sector. The Manufacturing Process Engineer will be responsible for developing, implementing, and improving manufacturing processes to achieve the highest standards of quality and efficiency. This role requires a deep understanding of engineering principles, advanced manufacturing techniques, and a strong commitment to innovation and continuous improvement.

Duties and Responsibilities

Process Development and Implementation

• Design and develop manufacturing processes for new products and optimize existing processes to improve quality and efficiency.
• Conduct feasibility studies and cost analyses for manufacturing projects.
• Collaborate with design, production, and quality teams to ensure seamless integration of new processes.
• Create detailed process documentation, including work instructions, process flow diagrams, and standard operating procedures.
• Transfer process knowledge to production teams.

Continuous Improvement

• Identify opportunities for process improvements and implement lean manufacturing principles to reduce waste and increase productivity.
• Analyze production data to identify trends and areas for improvement.
• Lead cross-functional teams in problem-solving and root cause analysis activities.
• Develop and implement corrective and preventive actions to address process deficiencies.

Quality Assurance

• Ensure that all manufacturing processes comply with industry standards and regulatory requirements.
• Work closely with the quality team to develop and implement quality control plans.
• Participate in internal and external audits and address any findings related to manufacturing processes.

Technical Support

• Provide technical support to production teams to resolve manufacturing issues and improve process performance.
• Train and mentor production staff on new processes and best practices.
• Collaborate with equipment vendors and suppliers to identify and implement new technologies and equipment.
• Maintain up-to-date knowledge of industry trends, technologies, and best practices.

Position Requirements

• Education Requirements: Bachelor’s Degree in Manufacturing Engineering, Mechanical Engineering, or related field.
• Experience Level Requirements : Minimum of 5 years of experience in manufacturing engineering, preferably in the precision engineering sector.

Skills Desired:

• Strong knowledge of manufacturing processes, materials, and equipment used in precision engineering.
• Experience with CAD/CAM software, ideally SolidWorks, MasterCam and other engineering tools.
• Knowledge of technical drawings and BOM.
• Proven ability to lead process improvement initiatives and implement lean manufacturing principles.
• Excellent problem-solving skills and attention to detail.
• Strong communication and interpersonal skills, with the ability to work effectively in cross-functional teams.
• Able to work under pressure with minimum supervision
• Knowledge of industry standards and regulatory requirements applicable to precision engineering.

SUMMARY

We are seeking a highly skilled and detail-oriented Process Engineer to develop, optimize, and maintain surface mount assembly processes for printed circuit board assemblies (PCBA). The ideal candidate will ensure high-yield, low-defect production by improving process capability, equipment utilization, and quality assurance.

ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.

• Develop and maintain SMT assembly processes (screen printing, pick-and-place, reflow soldering, Wave, SPI).

• Analyze and improve process capability (Cp, Cpk), first pass yield (FPY), and overall equipment effectiveness (OEE).

• Define, monitor, and optimize reflow oven thermal profiles for lead and lead-free soldering.

• Drive root cause analysis and corrective actions for process defects (e.g., tombstoning, solder bridging, head-in-pillow).

• Support New Product Introductions (NPI) by establishing process flows, documentation, and line setup.

• Perform DFM/DFT reviews with design and test engineering teams.

• Create and update standard operating procedures (SOPs), work instructions, and training materials.

• Work closely with cross-functional teams including quality, production, R&D, and equipment engineering.

• Ensure compliance with IPC-A-610, J-STD-001, ESD, and other industry standards.

MINIMUM REQUIREMENTS

1) Bachelor's degree in Electronics, Mechanical, Mechatronics, or Industrial Engineering (or related field).

2) 4–6+ years’ experience in SMT or PCBA manufacturing environment.

3) Strong knowledge of SMT machines.

4) Well verse on ISO 134854- Medical requirements. (Will be advantage)

SUMMARY

We are seeking a highly skilled and detail-oriented Process Engineer to develop, optimize, and maintain surface mount assembly processes for printed circuit board assemblies (PCBA). The ideal candidate will ensure high-yield, low-defect production by improving process capability, equipment utilization, and quality assurance.

ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.

• Develop and maintain SMT assembly processes (screen printing, pick-and-place, reflow soldering, Wave, SPI).

• nalyze and improve process capability (Cp, Cpk), first pass yield (FPY), and overall equipment effectiveness (OEE).

• D fine, monitor, and optimize reflow oven thermal profiles for lead and lead-free soldering.

• D ive root cause analysis and corrective actions for process defects (e.g., tombstoning, solder bridging, head-in-pillow).

• S pport New Product Introductions (NPI) by establishing process flows, documentation, and line setup.

• P rform DFM/DFT reviews with design and test engineering teams.

• C eate and update standard operating procedures (SOPs), work instructions, and training materials.

• W rk closely with cross-functional teams including quality, production, R&D, and equipment engineering.

• E sure compliance with IPC-A-610, J-STD-001, ESD, and other industry standards.

MINIMUM REQUIREMENTS

1) Bachelor's degree in Electronics, Mechanical, Mechatronics, or Industrial Engineering (or related field).

2) 4–6+ years’ experience in SMT or PCBA manufacturing environment.

3) Str ng knowledge of SMT machines.

4) Well verse on ISO 134854- Medical requirements. (Will be advantage)

Job Description

We are seeking a highly motivated and skilled Manufacturing Process Engineer to join our backend operations team. The successful candidate will be responsible for optimizing and maintaining the manufacturing processes for microarray production. This role involves working closely with cross-functional teams to ensure high-quality standards, efficiency, and continuous improvement in our manufacturing operations.

As a Process Engineer II, you will be an integral part of our team, responsible for sustaining and optimizing our microarray manufacturing processes. Your outstanding skills will help us achieve flawless efficiency, yield, and product quality. You will:

• Sustain, evaluate, and improve Backend manufacturing processes for microarray production.
• Implement process control techniques and procedures to ensure product quality and consistency.
• Identify areas for process improvement and lead initiatives to enhance efficiency and reduce costs.
• Work with Equipment Engineers to develop qualification plans detailing the steps and criteria for equipment testing and validation.
• Gather and analyze data from equipment trials to confirm performance against critical metrics.
• Prepare detailed reports summarizing the evaluation and qualification process.

We believe in continuous improvement and are determined to achieve world-class standards. You will:

• Provide technical support to the production team to troubleshoot and resolve manufacturing issues.
• Ensure all manufacturing processes align with standard operating procedures (SOPs) and regulatory requirements.
• Collaborate with quality assurance to implement corrective actions and preventive measures.
• Ability to work with cross-functional teams, including designers, suppliers, mold makers, and production staff.
• Strong communication skills to coordinate with suppliers, vendors, and other collaborators.

Your proven expertise and outstanding skills will help us compete at the highest levels. To be successful in this role, you should have:

• A Bachelor’s degree or equivalent experience in Engineering (Mechanical, Chemical, Biomedical, or related field).
• Experience with statistical process control (SPC), Design of Experiments (DOE), and other process engineering and quality improvement tools.
• Familiarity with cleanroom environments and relevant safety protocols.
• Excellent problem-solving, analytical, and project management skills.
• Strong communication and interpersonal skills.
• Experience with automated manufacturing systems and equipment.

Join us at Thermo Fisher Scientific Inc. and be part of a team that values collaboration, inclusion, and the relentless pursuit of excellence. Here, your contributions will make a real difference in advancing science and improving lives!

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Work Schedule

Environmental Conditions

Job Description

Are you a dynamic and driven professional eager to make a significant impact in the field of science? Thermo Fisher Scientific Inc. is in search of a Process Engineer II to join our innovative team! This role presents a ground-breaking opportunity to work with powerful technologies and be part of a world-class organization devoted to improving global health, sustainability, and safety.

As a Process Engineer II, you will be an integral part of our team, responsible for sustaining and optimizing our microarray manufacturing processes. Your outstanding skills will help us achieve flawless efficiency, yield, and product quality. You will:

• Sustain and optimize microarray manufacturing processes to improve efficiency, yield, and product quality.
• Identify and implement process control techniques and procedures to ensure product quality and consistency.
• Work closely with Product Development and multi-functional teams to transition new products from development to production.
• Prepare technical reports, process documentation (process verification and validation), and standard operating procedures (SOPs).

We believe in continuous improvement and are determined to achieve world-class standards. You will:

• Sustain and optimize microarray manufacturing processes to improve efficiency, yield, and product quality.
• Identify and implement process control techniques and procedures to ensure product quality and consistency.
• Work closely with Product Development and multi-functional teams to transition new products from development to production.
• Prepare technical reports, process documentation (process verification and validation), and standard operating procedures (SOPs).

Your role is pivotal in ensuring our production processes run smoothly and efficiently. You will:

• Resolve process-related issues to minimize downtime and ensure smooth production flow.
• Ensure all manufacturing processes align with standard operating procedures (SOPs) and regulatory requirements.
• Collaborate with quality assurance to implement corrective actions and preventive measures.

Your proven expertise and outstanding skills will help us compete at the highest levels. To be successful in this role, you should have:

• A degree or equivalent experience in Chemical Engineering, Materials Science, Mechanical Engineering, or a related field with a minimum of 3 years working experience in process engineering, preferably in semiconductor, biotechnology, or microfabrication industries.
• Experience with statistical process control (SPC), Design of Experiments (DOE), and other process engineering and quality improvement tools.
• Familiarity with cleanroom environments and relevant safety protocols.
• Excellent problem-solving, analytical, and project management skills.
• Strong communication and interpersonal skills.
• Experience with automated manufacturing systems and equipment.
• Knowledge of regulatory requirements and standards (e.g., ISO, FDA) will be highly advantageous.

Join us at Thermo Fisher Scientific Inc. and be part of a team that values collaboration, inclusion, and the relentless pursuit of excellence. Here, your contributions will make a real difference in advancing science and improving lives!

CDI

Job Description:

• Contribute to Life Science projects for Antaes Asia clients
• Perform and review process engineering drawings and calculations, including but not limited to (heat exchanger sizing, pump selection, piping design, control valve sizing, heat and mass balances, and other engineered calculations).
• Verify and validate calculations provided by vendors, clients, and other consultants to ensure accuracy and compliance with industry standards.
• Prepare and review technical data sheets for various equipment, instrumentation, and systems used in biologics manufacturing.
• Ensure all documentation aligns with the project’s technical requirements and industry best practices.
• Support the preparation and review of risk assessments, including Hazard and Operability Studies (HAZOPs), to identify and mitigate potential risks in the process design and operation.
• Collaborate in the preparation and review of automation sequences required for process automation, ensuring seamless integration with existing systems and compliance with regulatory requirements.
• Work closely with other engineering disciplines and cross-functional departments such as automation engineering, facilities engineering, validation, project management, operations, quality, and safety.
• Facilitate effective communication and coordination to ensure project success and alignment with overall business goals.
• Review Commissioning Project Plans, Validation Project Plans, Design Qualifications, Traceability Matrices, Commissioning Protocols, Qualification Protocols, and Validation Protocols for pharmaceutical equipment and systems.
• Ensure that all client process equipment and facilities operate as intended to meet biopharmaceutical manufacturing requirements.
• Provide ongoing support to the client’s plant operations, ensuring that engineering projects align with the changing needs of the business.
• Manage upstream and downstream equipment, as well as other unit operations, to optimize production efficiency and product quality.
• Implement projects addressing Corrective Actions/Preventative Actions (CAPA) identified during deviation investigations, requests from value stream stakeholders, or GMP audits.
• Offer on-the-floor troubleshooting support for manufacturing operations, with a focus on resolving equipment-related issues.
• Raise and lead GMP change requests for implementing changes to equipment and facilities, ensuring compliance with Good Manufacturing Practices (GMP).
• Adhere to all applicable Environmental, Health, and Safety (EHS) requirements, ensuring that engineering activities support a safe and compliant workplace.
• Contribute to the promotion of Antaes services on top of assistance provided to clients

Job Requirements:

• Bachelor’s Degree in Biomedical Engineering, Biotechnology, Science or equivalent
• Minimum 2+ years of pharmaceutical, biopharmaceutical experience in Process Engineering and/ or Compliance (GxP) environment
• Ability to quickly know products and processes in order to assess quality issues
• Candidate must be highly motivated, be able to work independently as well as in a team and have good organizational and oral and written communication skills
• Demonstrated good knowledge of technical drawings, general arrangement drawings, and equipment design drawings (P&ID) is required.
• Experience in the design and operation of biopharmaceutical manufacturing equipment and facilities.
• Experience in the management and coordination of engineering and construction management consultants, equipment vendors and contractors.
• Excellent communication skills, both written and verbal, in English

Element Solutions Inc (NYSE: ESI) is a leading specialty chemicals company whose operating businesses formulate a broad range of solutions that enhance the performance of products people use every day. Developed in multi-step technological processes, our innovative solutions enable our customer’s manufacturing processes in several key segments, including electronic circuitry, communication infrastructure, automotive systems, industrial surface finishing, consumer packaging, and offshore energy.

Customers of our businesses use our innovation as a competitive advantage, relying on us to help them navigate in fast-paced, high-growth markets. For example, in-car technology, from infotainment to driver assistance, is accelerating the pace of new product development and changing the competitive playing field for automotive manufacturers. With a long-standing presence in automotive markets and a deep market expertise in electronics, we sit at the intersection of this fast-growing market.

We strive to embody the five “Elements of our Culture,” our “5Cs”: Challenge, Commit, Collaborate, Choose and Care. These core values are the foundation of our organization which our employees embrace in their interactions with customers, colleagues and other stakeholders to drive financial performance and create a rewarding work environment.

MacDermid Alpha Electronics Solutions, a business of Element Solutions Inc (NYSE: ESI), is renowned worldwide for its commitment to revolutionizing the electronics industry. With a legacy spanning over a century, we have continually set new benchmarks for excellence, reliability, and sustainability in electronic materials.

The primary purpose of this position is to provide global technical, managerial, and supervisory direction to develop new processes and improve existing processes for optimization of chemical manufacturing processes by working with the regional and functional leaders to identify and execute projects that can improve productivity, efficiency, quality, and reduce the overall cost of operations.

• Support and lead optimization projects – Responsibilities include the planning, coordination, communication and execution of optimization projects related to chemical processes.
• Support and lead the sharing and implementation of best practices within the region.
• Provide technical, managerial and supervisory direction to develop new guidelines and procedures for scale-up of newly developed products and technology transfers.
• Provide technical and managerial direction for special projects of a complex nature requiring engineering and technical expertise.
• Responsible for the development of new processes to reduce process cycle time and improve quality and yield of finished goods.
• Motivate team to achieve Key Performance Indices (KPI) set by management.
• Lead taskforce to overcome production and quality issues.
• Any other tasks that are assigned.

• Bachelor’s degree in Chemical Engineering or related disciplines.
• Relevant industrial experience of about 2 to 5 years in a chemical manufacturing environment.
• Proven track record of working in an operations/supply-chain organization, along with effective engagement with cross-functional teams.
• Strong leadership, program/process management, analytical, and communication skills.
• Ability to lead, coach and inspire a team independently of formal authority.
• Manage multiple priorities and tasks simultaneously.
• Maintain tight timelines while meeting targeted savings outcomes.
• Experience with total cost of ownership reduction and process improvement.

• Six Sigma Green Belt with statistical analytical skills preferred.
• Ability to read and create piping and instrumentation (P&ID) diagrams.
• Possess or have knowledge in ISO 9001 and ISO 14001.

As part of our team here, as well as receiving a competitive base salary, you will also participate in a generous performance-related bonus scheme. In addition, you will also be covered under our corporate medical insurance plan and annual leaves.

At ESI, you will be part of a highly collaborative culture that promotes continuous improvement through cross-functional partnerships to achieve our mission. We do this through a strong and unified culture and transparent management which has empowered us to create high performing global teams that achieve superior solutions for our customers.

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.