Manufacturing Eng - P2 at Boston Scientific Corporation Malaysia

, , United States -

Full Time

Start Date

Immediate

Expiry Date

06 Mar, 26

Salary

0.0

Posted On

06 Dec, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Manufacturing Support, Process Optimization, Equipment Troubleshooting, Root Cause Analysis, Non-Conforming Product Evaluation, Technical Activities, Problem Solving, Process Improvement, Mechanical Design, Automation, FDA Regulations, Medical Device Industry, Bilingual, Engineering Principles, Project Management, Cross-Functional Interaction

Industry

Medical Equipment Manufacturing

Description

Provides support to the Manufacturing organization to facilitate efficient operations within the production area, to optimize existing processes, and to ensure that production goals are met. Support manufacturing basic daily activities and/or continuous improvement projects such as; equipment troubleshooting, root cause analysis and non-conforming product evaluation. Initiates and completes technical activities leading to new or improved products or process, for current programs, next generation programs and to meet strategic goals and objectives of the company. Prepares reports, publishes, and makes presentations to communicate metrics and/or findings. Analyzes and solves problems from basic engineering principles, theories and concepts through to a wide range of complex and advanced problems which require novel and new innovative approaches or a major breakthrough in technology. Understands engineering principles theories, concepts, practices and techniques. Develops knowledge in a field to become a recognized area expert in the assign area (manufacturing process, equipment technology and/or projects)and applies this knowledge in leadership roles in the company. Incorporates business policies and procedures into task completion. Understands the business needs of the company, and has knowledge of the customer needs of our business. Understands the business cycle and foresight of emerging technologies trends. Assesses process capabilities, prioritizes process improvements opportunities, and innovates and implements process improvements on commercial products. Writes and reviews validations protocols and reports applicable to new processes. Cultivates internal and external network of resources to complete tasks. Serves has a resource in the selection orientation and training of new engineers and employees. Interacts cross functionally and with internal and external customers. Serves as a consultant for engineering or scientific interpretations and advice on significant matters. BS Mechanical/Electrical Eng. with 2 + years of related experience or an equivalent combination of education and work experience Experience in mechanical design and or automation preferred. Previous experience in an FDA regulated industry is a plus. Knowledge on Problem Solving / Process Improvement Methodology applied to job experience. Medical Device industry job experience preferred. Fully Bilingual (English/Spanish)

Responsibilities

The role involves supporting manufacturing operations, optimizing processes, and ensuring production goals are met. It includes troubleshooting equipment, conducting root cause analysis, and leading continuous improvement projects.