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PFMEA Manufacturing Engineer - (NO C2C OR THIRD PARTY)

Company:
Kelly Science, Engineering, Technology & Telecom
Location:
Batesville, IN, 47006
Posted:
June 07, 2025
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Description:

PFMEA Manufacturing Engineer - (NO C2C OR THIRD PARTY)

Location: Onsite – Batesville, Indiana (47006)

Duration: 12 months - (Contract extension possibility)

Pay: Negotiable depending on DIRECT RELATED experience with PFMEA and manufacturing within medical device environments.

Type: W2 ONLY contract (NO C2C OR THIRD PARTY)

JOB SUMMARY:

Design, develop, evaluate or improve assembly systems or related processes, including human work factors, quality control, inventory control, material flow, cost analysis, and production coordination. May work with commercial or industrial designers to refine process designs to increase productivity and decrease costs.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Create and update documentation for PFMEA, job instructions, and standard operating procedures.

Read and interpret blueprints, technical drawings, schematics, or computer-generated reports.

Identify opportunities or implement changes to improve products or reduce costs using knowledge of assembly processes, tooling and production equipment, assembly methods, quality control standards, or product design, materials and parts.

Troubleshoot new or existing product problems involving designs, materials, or processes.

Provide technical expertise or support related to manufacturing.

Confer with engineers or other personnel to implement operating procedures, resolve system malfunctions, or provide technical information.

Determine root causes of failures using statistical methods and recommend changes in designs, tolerances, or processing methods.

Perform nonconforming material analysis.

Work with Quality Control on reducing the NCMRs.

Plan and establish sequence of operations to assemble parts or products and to promote efficient utilization.

Ensure safety procedures are followed, work areas are clean and maintained, and the department is following regulatory compliance requirements.

Apply continuous improvement methods such as lean manufacturing to enhance manufacturing quality, reliability, or cost-effectiveness.

Supervise the work of technicians and other associates as needed.

Important information: To be immediately considered, please send an updated version of your resume to .

*** (Kelly does not expense relocation/interview costs)**

Work Authorization: Must be currently in the United States with active employment authorization documents.

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