Job Description

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:

Responsible for supporting product transfer, instrument manufacturing, troubleshooting, failure analysis, quality improvement, process enhancement, cost reduction, engineering evaluation and system improvement.

Tasks and Responsibilities:

• Manages NMPA regulated or RUO projects
• Helps drive execution on project goals through leadership on a cross-functional, matrixed team
• Manage projects includes creation and maintenance of detailed project plans and schedules for team members, provide status reports and make presentations to stakeholders
• Developing project scopes and objectives, involving all relevant stakeholders and ensuring technical feasibility
• Coordinate/support operation readiness with Engineering, Supply Chain, Quality and Manufacturing to ensure successful pilot build, early access, and first customer shipment. Conduct post build reports and review, and support sustaining activities
• Drive troubleshooting, failure analysis, root cause analysis, issues closure and corrective action processes as required
• Drive and implement process improvements and product sustaining activities to meet the production goals
• Apply various analysis techniques, such as FMEA and statistical analysis to optimize product quality and minimize cost, providing all calculations, performance data, and drawings required on new and existing products
• Manage and coordinate Engineering Change Order implementation activities including scrap analysis, material disposition, update work instructions and test requirement changes
• Documentation responsibilities include, but not limited to, generating detailed engineering drawings, Bill of Materials, test reports, assembly procedures and design validation plans
• Work closely with internal teams and external partners e.g. contract manufacturers and key partners to ensure smooth transition of quality products from development into manufacturing
• Regional travel required to support our manufacturing partners

All listed tasks and responsibilities are deemed as essential functions to this position; however, business conditions may require reasonable accommodations for additional tasks and responsibilities.

Preferred Education:

• Bachelor\'s degree or Master in Mechanical or Electro-mechanical Engineering

Preferred Requirements:

• 5+ years of engineering experience in mechanical or electro-mechanical based products for commercial and industrial markets
• Good working knowledge and experience in mechanism design and electro-mechanical systems
• Strong organizational skills, attention to detail and accuracy, and the ability to work independently in a team environment are essential
• Candidate must be able to effectively lead teams, interface well with the manufacturing and service organization, and has a proven track record of transferring products to manufacturing
• Must possess good analytical and troubleshooting skills
• Working knowledge and application of problem solving techniques such as 8D, KT, FMEA
• Proficient in engineering tools such as, statistical analysis, design of experiments, product and process capability analysis
• Proficient in Solidworks or 3D CAD tools, and MS Project
• Good working knowledge of BOM (Bill-Of-Material) structuring fundamentals and have the ability to create ECOs (Engineering Change Order) and Deviations
• Demonstrated use and understanding of MRP systems, Product Data Management systems and Change Control processes. SAP & PLM experience will be added advantage
• Experience with FDA regulated medical device product development preferred
• Experience with OEM partnership is preferred
• Product development experience in the life sciences, biotech, biomedical, nanotechnology or semiconductor industries preferred

Illumina believes that everyone has the ability to make an impact, and we are proud to be an equal opportunity employer committed to providing employment opportunity regardless of, race, creed, color, gender, religion, marital status, domestic partner status, age, national origin or ancestry, physical or mental disability, medical condition, sexual orientation, pregnancy, military or veteran status, citizenship status, and genetic information.

Additional Information

Career Level

Senior Executive

Qualification

Bachelor\'s Degree, Post Graduate Diploma, Professional Degree, Master\'s Degree

Years of Experience

5 years

Job Type

Full-Time

Job Specializations

,

Company Overview

At Illumina, we\'re making genomics more useful for all, for a better understanding of human health. By shining a brighter light on genomics, together we can harness the power to build a stronger world.
From our earliest startup days, we\'ve always aspired to transform human health. Each new product is designed to empower our community to explore DNA at an entirely new scale, and discover answers to life\'s biggest questions. Like what causes a cancer cell to mutate? What\'s the origin of a puzzling disease? Is it possible to prevent the next outbreak? Or safeguard the world\'s food supply? These challenges inspire us to push the boundaries of what\'s possible, and connect more people to the technology and insights changing the world.
Today we\'re a global leader in genomics-an industry at the intersection of biology and technology. We\'re passionate about helping our customers read and understand genetic variations through our increasingly accessible, simple solutions. The advances our solutions support are triggering a fundamental shift in healthcare and beyond. Medicine will continue to become more preventive and more precise. We will be healthier, longer. And we\'ve only just begun.

Additional Company Information

Registration No.

200310311H

Company Size

501 - 1000 Employees

Average Processing Time

30 days

Industry

BioTechnology/Pharmaceutical/Clinical research

Singapore Post