Position Title
Manufacturing Process Engineer
SBU
OEM
Department
Engineering
Relocation Covered
NO
Educational Requirements
Bachelor's degree
Experience Requirements
Minimum of five years' experience as a manufacturing engineer in a machine shop environment.
Qualification Requirements
Bachelors degree or the equivalent of in related field.
Preferred Qualifications
Lean Six Sigma background preferred. Medical industry background preferred.
Responsibilities
The Manufacturing Engineer is responsible for managing the process, understanding capacity, capability, quality and driving continuous improvement. Reviews and improves product quality by developing solutions to production problems, equipment and engineering designs. Implements cost reduction plans. This position must be familiar with standard concepts, practices and procedures. Relies heavily on experience and judgment to plan and accomplish goals. Works under minimal supervision.
DUTIES AND RESPONSIBILITES:
Develop manufacturing processes and CNC programming to optimize manufacturing times including cycle and processes.
Implement cost reduction by working closely with manufacturing to reduce scrap and waste
Develop routing and standard times.
Assists in design reviews.
Lead person for FMEA's
Design and assist in the manufacturing of product.
Implement deviations/ECN documents and route through approval and release.
Provides assistance for quotations.
Develops Control Plans
Assists in MRP's
Determine equipment needs and create cost justification.
Write and perform equipment validations.
Other duties as assigned
SKILLS / KNOWLEDGE
Experienced blue print reader and GD&T knowledge.
Knowledge of CAD CAM for designing and manufacturing.
Experience in the area of manufacturing operations, process validations and statistics.
Possesses experience in transferring product from pilot to production, analyze discrepant product and implement CAPA's.
Good oral and written communication skills.
Ability to initiate, prioritize and drive projects to completion
Work independently.
Familiar with the design cycle and FDA documentation requirements, QSR, GMP.
Knowledge of process improvement methodology.
Ability to write and perform IQ's, OQ's and PQ's.
