Engineer 2, Process Development

What if the work you did every day could impact the lives of people you know? Or all of humanity? At Illumina, we are expanding access to genomic technology to realize health equity for billions of people around the world. Our efforts enable life-changing discoveries that are transforming human health through the early detection and diagnosis of diseases and new treatment options for patients. Working at Illumina means being part of something bigger than yourself. Every person, in every role, has the opportunity to make a difference. Surrounded by extraordinary people, inspiring leaders, and world changing projects, you will do more and become more than you ever thought possible. Position Summary: Be part of a highly dynamic and competent Engineering Team who is responsible to meet the quality, productivity and cost targets in a high volume, multi-product and life science regulated environment through developing effective world class engineering solutions. Responsible for new product introduction and production support engineering for a specific product or group of products after transferring from design to in-house or outsourced production. Interfaces with design, process, test, reliability and manufacturing engineering to solve product issues and production problems. Develops and sustains process improvements to reduce production costs and increase yields. Position Responsibilities: 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. Provides advanced failure analysis, root cause identification and corrective actions for product quality concerns and/or issues during manufacturing and NPI ramp. Analyzes field quality data to identify areas for prevention and improved detection 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 All listed tasks and responsibilities are deemed as essential functions to this position; however, business conditions may require reasonable accommodation for additional tasks and responsibilities Position Requirements: Bachelor's Degree or Master's Degree in Engineering/Science in Chemistry, Mechanical, Electrical, Biomedical, Material or a related field. Minimum 2 years of work experience, preferably in the biotech industry Experience in FDA-regulated environment is a plus. Knowledge about wafer fabrication, biochemistry process, plastic engineering, 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 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. Competencies: Core Technical Leadership - Demonstrates leadership in the development of technical innovations and in ensuring optimum collaboration and knowledge sharing of technical insights. Project Leadership & Troubleshooting - Actively works to resolve project challenges and facilitate knowledge transfer between team members focused on shared objectives. Technical Breadth/Depth - Demonstrates motivation to build deeper technical depth in area-of-expertise, and inform that knowledge base through understanding of associated areas. Customer-Centric Focus - Ensures that a positive customer experience informs both ... (truncated, view full listing at source)