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Hologic, Inc. · 2 weeks ago

Value Improvement Project Engineer 2

Newark, DE

Full-time

Onsite

Entry, Mid Level

$79K/yr - $120K/yr

1+ years exp

Hologic, Inc. is a high growth world-class manufacturing facility focused on life-saving medical devices. The Value Improvement Project Engineer is responsible for supporting the execution of value improvement projects into manufacturing, coordinating teams and driving project execution from scoping through implementation.

BiotechnologyHealth CareHealth DiagnosticsWomen's

Comp. & Benefits

H1B Sponsor Likely

Responsibilities

Actively manages projects from initiation through completion including completing cost: benefit analysis, defining project scope, creating and maintaining project schedule, and providing updates to stakeholders

Conduct product cost analysis of tact time, labor and burdened costs for input into COGS

Completes analysis of projects to assess resource allocation to identify and prioritize projects based on value proposition

Participates in and supports activities such as Standard Operating Procedures and Agile creation and maintenance, Defect Reviews, DFMEA Meetings, DFMEA document review, Kaizen Events, and Process Enhancement Activities

Continuously work to improve manufacturing methods, efficiency, and product quality

Participates in design reviews and provides technical support to R&D on manufacturing processes

Collaborate with R&D on BOM structure, including subassembly breakout and make/buy determinations

Collaborates with production to deliver a manufacturing process which incorporates production requirements into manufacturing process design

Active contributor in design implementation projects translating improved product designs from design engineering to manufacturing

Define and develop assembly and test methods as they relate to design transfers and/or new supplier qualification

Specify and design all necessary tools, equipment, and fixtures required to support projects

Creates work instructions, bills of material, technical drawings and manufacturing documentation

Creates and manages engineering change orders through the implementation of the project

Develops, verifies, and validates process for manufacturing

Creates and maintains process flowcharts, Risk Files & Process Control plans

Participate in risk mitigations and risk management activities related to manufacturing improvements including PFMEAs

Coordinates and develops user manuals, training materials and other documents required for knowledge transfer to process owner

Monitor initial production run quality and output and uses problem solving skills to identify trends, investigate problems and perform root cause analysis. Recommends and implements corrective action plans as it relates to projects

Evaluate and develop process controls data for trending analysis

Provides regular communication and updates on project status

Provide inputs into analysis for new supplier selections based on core competencies and experience

Actively supports and adheres to the Quality Policy and QMS procedures following Good Documentation Practices (GDP)

Qualification

Cost AnalysisProcess ImprovementProject ManagementManufacturing MethodsRisk ManagementTechnical DocumentationCollaborationProblem SolvingCommunication

Required