Supplier Process Engineer - MP IA&E

Our Client, an American Biotechnology company, is looking for a Supplier Process Engineer - MP IA&E for their Sunnyvale, CA location.


Responsibilities:

• Work with suppliers and ISI engineering for the new product introduction to
• Complete part production qualification process ( PPQP), which includes but not limited to delivering on the following deliverables: spFMEA, Special Process Validations, Process capability, capacity analysis ,and FAIR .
• Develop supplier ramp readiness based on forecast, supplier capacity, quality performance, and process capability.
• Perform DFM by engaging suppliers early in development cycle to feedback manufacturability improvements in the designs prior to production
• Lead and resolve the supply continuity/ quality issues at suppliers through in-depth root cause and corrective actions utilizing SCARs, SCRs (Supplier Change requests) and VR processes.
• Monitor supplier performance and initiate improvement activities.
• Drive suppliers to continually improve their business and manufacturing process performance to meet client's requirements for supplier excellence including ship to stock programs using a collection of best practices in project management, Six Sigma, Lean, SPC and negotiation by leading these efforts without managerial guidance at several suppliers simultaneously.
• Develop and use metrics for supplier part cost, delivery, quality, capacity and capability by creating metrics to measure real improvement and judge required intervention or change at the supplier or in a commodity.
• Driving change to ISI specifications as necessary by understanding and changing specifications and drawings including driving the ECO process to implementation.
• Prepare and deliver supplier communications as required by independently working with suppliers on scorecard creation of QBRs, Supplier Summits, etc.
• Identify and investigate opportunities for cost reduction and/or quality improvement by judging opportunities and creating strategies to seize those opportunities, completes research and provides data-driven plans to management.

Requirements:

• BS degree in Engineering or equivalent, master's degree preferred
• Min. 4 years of related experience in an engineering function. Internship and Co-Op experience is acceptable.
• Basic knowledge of mechanical manufacturing process like injection molding, machining, thermoforming, stamping or related field highly preferred.
• Hands-on experience with these processes is preferred.
• Internship and Co-Op experience is acceptable.
• Understanding of basic level of statistical techniques including capability analysis and normality.
• Ability to read and interpret detailed mechanical drawings and communicate technical information. Experience with GD&T is preferred.
• Excellent problem solving and organizational skills
• Excellent written and verbal communication skills including presentations to various levels of management
• Significant computer experience using Windows, Word, Excel, Minitab, PowerPoint, Confluence, and other engineering/collaboration tools.
• Experience in a medical device company is a plus.

Why Should You Apply?

• Health Benefits
• Referral Program
• Excellent growth and advancement opportunities

ICONMA is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to any status protected by applicable law.