Develops and modifies process formulations, methods and controls to meet quality standards Typically performs one or more of the following in capacity of either an individual contributor (as directed and/or independently), or as a manager:
• Create, analyze and review technical charts
• Develop and modify process formulations, methods and controls to meet quality standards
• Establish SOP (Standard operating process) and FMEA (Failure mode and effects analysis) for related process
• Review product development requirements for compatibility with processing methods to determine costs and schedules
• Integrates equipment and material capabilities to meet process module and technology specifications
• Drive CIP (Continuous improvement plans) to improve process performance indices
• Work with cross functions teams to deliver organizational goals • Perform all activities in a safe and responsible manner and support all Environmental, Health, Safety & Security requirements
• Work and collaborate other projects and/or assignments as needed
See description for career level for general proficiency levels pertaining to Job Complexity, Accountability, Relationship Focus, and Knowledge, Skills & Abilities. These proficiency levels apply to all career levels. Some requirements may vary locally.
Key Responsibilities
- Perform process sustaining tasks on 12-hours shifts (morning & night) such as holding lots dispositions, shift pass-down, alarm recovery, tool set-up data review, SPC/FDC/YDD out-of-control inhibits and checking, data analysis and compilation, and tasks claim as assigned by supervisors.
- Process Qual handling and interpreting Implant Qual data
- Perform beam tuning according to (SOPs) and respond to beam tuning related alarm
- Troubleshoot process related issues. Act as a first line of defense in the module and in responding to process, equipment and measurement abnormality and deviations.
- Monitor and analyze Statistical Process Control (SPC) charts using SPACE and other tools; respond to process deviations and follow corrective action systems (CAS). Perform tasks according to out-of-control OCAP, Corrective Action System (CAS) with mindset of quality come-first.
- Assist in lot disposition and data collection for process and equipment faults; ensure accurate documentation and pass down.
- Collaborate with Engineers and Specialists on process qualifications, experiments (e.g., R&R runs, DOE), and improvement projects.
- Execute Standard Operating Procedures (SOPs) and maintain compliance with safety and environmental guidelines.
- Contribute to scrap reduction initiatives and uphold high standards of operational discipline.
- Ensure safety, discipline, and housekeeping compliance in work area by all personnel.
- Comply with environmental, health, safety and security (EHSS) system, policies, procedures and guidelines that are applicable to your scope of work and workplace.
Requirements
- Good communication in English is required
- Teamwork abilities.
- Willingness to work on rotating shifts.
- Eagerness to learn and grow in a fast-paced, high-tech manufacturing setting.
Development Opportunities
- Structured training and mentorship from experienced engineers/senior Process AE
- Exposure to cross-functional teams and various modules.
- Opportunities to participate in innovative and improvement projects.
Education
- Diploma in Electrical, Electronics, Mechanical, Mechatronics, Microelectronics, Chemical Process Engineering, Chemistry, Physics, or any other relevant engineering discipline.
Experience
- Implant experience is preferable
- Fresh graduates are encouraged to apply
- Other essential attributes
- Perform 12-hours rotating shift
- Team Player
- Good ownership and accountability
- Good verbal and written communication skills
- Flexible and able to support overtime
