Manufacturing Eng - P3

Boston Scientific
11d

About The Position

Evaluates, selects, and applies standard engineering techniques, procedures, and criteria, using judgment in making minor adaptations and modifications. 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. Participates in project teams typically including one of the following: 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; and other activities of limited scope requiring knowledge of principles and techniques commonly employed in the specific narrow area of assignments. Participate in equipment and process validation. Participate in equipment and process validation. Coordinates with the appropriate suppliers and other external resources needed in developing and implementing process/product improvement plans. Perform root cause analysis of failed product. Participates in project planning and scheduling. Perform responsibilities required by the Quality System and other duties as assigned or requested.

Requirements

  • BS Mechanical/Electrical Eng preferred with 3 + years of experience or an equivalent combination of education and work experience
  • Knowledge on Problem Solving / Process Improvement Methodology applied to job experience.
  • Fully Bilingual (English/Spanish)

Nice To Haves

  • Experience in mechanical design and or automation preferred.
  • Previous experience in an FDA regulated industry is a plus.
  • Medical Device industry job experience preferred.

Responsibilities

  • Evaluate, select, and apply standard engineering techniques, procedures, and criteria.
  • Improve existing manufacturing processes.
  • Act as liaison between production and engineering group.
  • Assist with the introduction of new products into the Operations production area.
  • Participate in project teams for process/product improvement.
  • Design, perform, and document engineering test experiments.
  • Participate in Quality improvement activities.
  • Design, develop, test, and validate equipment, tools and fixtures.
  • Analyze and interpret process models and recommend process improvements.
  • Evaluate external process technologies.
  • Participate in equipment and process validation.
  • Coordinate with suppliers and external resources.
  • Perform root cause analysis of failed product.
  • Participate in project planning and scheduling.
  • Perform responsibilities required by the Quality System.

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What This Job Offers

Job Type

Full-time

Career Level

Mid Level

Number of Employees

5,001-10,000 employees

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