Manufacturing Engineer

Role: Manufacturing Engineer

Location: Connecticut

Job Details

Our Medical Device Client is looking for a MFG Engineer to support their current project needs.

Immediate expectations:

• Under the guidance of the Engineering leadership, work to improve performance of manufacturing systems, e.g. OEE improvement (quality, performance and uptime), maintenance needs, MUV and scrap reduction
• Support project timelines and milestones and bring them to completion on time and within budget
• Assist in completion of CAPA tasks and deliverables (Corrective and Preventive)
• Use methodical approach for root cause analysis and propose robust technical solutions
• Process technical expert for a manufacturing production line
• Create and edit documents to support Production
• Support initiatives for continuous process and product improvements
• Conducts independent analysis and develops solutions to problems.
• Develops approaches and designs where precedent usually exists
• Performs developmental and/or test work that relies heavily on a comprehensive knowledge of theory and design
• Receives general project direction. Solicits input from more experienced engineers.
• Work on special projects as they arise

Long term expectations:

• Initiate and manage projects with adherence to program-management guidelines
• Develop innovative tool design improvements
• Develop and characterize processes and summarize technical details
• Work with Quality Engineers on qualification activities for new or modified processes and equipment.
• Assists in training new/current employees with respect to documentation, use of equipment, laboratory techniques and department procedures.
• Delivers communications tailored to the needs of the receiver (managers, peers, customers) with appropriate frequency to maximize its utility and promote cross-functional collaboration.

Knowledge & Skills

• General understanding of automation, plastic injection molding, part assembly, fixturing, testing, and process control techniques
• Six-Sigma Methodology (DOE, Process Capability, Gage R&R, etc.)
• Knowledge of the Medical Device Industry and familiarity with FDA QSR Regulations – preferred
• Proficiency in SolidWorks. Mechanical understanding, tool design experience
• Technical writing competency
• Requires the ability to independently make decisions that impact the attainment of project objectives.
• Bachelor’s degree from an accredited college or university (Engineering or Technology)