Manufacturing Eng - P3

Boston Scientific•,

1d•$58,100 - $110,400

About The Position

At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions. Manufacturing Eng – P3 (Mfg Engineer III) Evaluates, selects, and applies standard engineering techniques, procedures, and criteria, using judgment in making minor adaptations and modifications. Assignments have clear and specified objectives and require the investigation of a limited number of variables. Improve existing manufacturing processes and act as liaison between production and engineering group in resolving problems encountered on the production floor. Assist with the introduction of new products into the Operations production area.

Requirements

BS Mechanical/Electrical Eng preferred with 3 + years of 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

Identifying and implementing process/product improvement alternatives to increase/optimize yield, efficiency, throughput, and/or performance.
Designing, performing, and documenting engineering test experiments to evaluate product/product performance.
Participating in Quality improvement activities.
Designing, developing, testing, and validating equipment, tools and fixtures.
Analyzing and interpreting process models and recommending process improvements.
Evaluates external process technologies.
Participate in equipment and process validation. Write protocols and reports for Equipment Installation Qualification, Operational Qualification and Process Performance Qualification.
Has working knowledge of Risk Management & Failure mode and effect analysis (FMEA) requirements.
Interfaces with assemblers, production supervisors, and engineers in troubleshooting problems on the production floor.
Coordinates with the appropriate suppliers and other external resources needed in developing and implementing process/product improvement plans.
Acts independently to implement and follow through.
Perform root cause analysis of failed product.
Participates in project planning and scheduling.
Optimize processes for yield improvements, cycle time improvements, and scrap reduction.
Attends and contributes to product core team meetings.
Perform responsibilities required by the Quality System and other duties as assigned or requested.