Illumina

Process Integration Engineer 2 (Contract Manufacturers Operation)

Illumina
BiotechSingapore - Woodlands - NorthTechFull-time5 days ago

About the role

AI summarised

Process Integration Engineer responsible for managing Illumina consumable product portfolio at contract manufacturers worldwide. Leads failure analysis, drives capacity improvement, and collaborates with R&D on design-for-manufacturing in a biotech/semiconductor environment.

BiotechFull-timeGeneral

Key Responsibilities

  • Lead and manage Illumina consumable product portfolio, with focus on contract manufacturer's operation at worldwide locations.
  • Provides advanced failure analysis, root cause identification and corrective actions for product quality concerns and/or issues during manufacturing and NPI ramp with internal stakeholders and contract manufacturers.
  • Analyze field quality data to identify areas for prevention and improved detection.
  • Drive capacity improvement and expansion plan to meet volume ramp. Including identification of high-volume manufacturing solutions and qualification of new tools.
  • Work closely with R&D to develop Design-for-Manufacturing (DFM) processes for NPI, leveraging learning from existing products and providing feedback on material component selection and associated test plans.
  • Experience with using engineering tools and software packages to test, design and evaluate products and manufacturing margins.
  • Proactively drives process improvement activities through FMEA to ascertain and recommend improvement to processes or test methods.
  • Ability to interpret test results and correlate results with product failure performance

Requirements

  • Bachelor's Degree or Master's Degree in Engineering/ Science in Chemistry, Mechanical, Electrical, Biomedical or Material or a related field
  • Minimum 2 years of work experience in the biotech industry is strongly preferred.
  • Prior experience in process integration or product engineering within a semiconductor manufacturing environment is preferred.
  • Experience in FDA-regulated environment is a plus.
  • Knowledge about wafer fabrication, biochemistry process, back-end packaging assembly, or CMO Management will be an added advantage.
  • Possess good understanding of manufacturing processes, methodologies and environment.
  • Capable of defining test plans for components, materials and systems
  • Skilled in yield engineering, continuous improvement and failure analysis of multiple reliability failure modes
  • Excellent Analytical, Problem Solving and Project Management skills.
  • Good understanding of Quality Assurance and Process Control Knowledge.
  • Excellent team player, interpersonal and communication skills.
  • Able to work well under stress, both internally and across functions and perform multitasking.
  • Proactive, innovative and self-motivating.
  • Willingness to travel in support of supplier management and coordination.