PFMEA Manufacturing Engineer - (NO C2C OR THIRD PARTY)

Kelly Science, Engineering, Technology & Telecom; Batesville (IN); On-site; USD 67,000 - 124,000; Full time

Job summary

A leading company seeks a PFMEA Manufacturing Engineer in Batesville, Indiana, to design and improve assembly systems in medical device manufacturing. The role involves enhanced documentation, technical troubleshooting, and applying continuous improvement methods to achieve quality and cost-effectiveness. Applicants must possess substantial experience in PFMEA within a manufacturing context.

Benefits

Medical insurance

Vision insurance

401(k)

Qualifications

• Experience with PFMEA and manufacturing processes is essential.
• Ability to troubleshoot designs and processes.
• Knowledge of assembly methods, tooling, and production equipment.

Responsibilities

• Design and improve assembly systems and processes.
• Create and update documentation for job instructions.
• Implement changes to improve products or reduce costs.

Skills

Quality Control

Cost Analysis

Process Improvement

Technical Expertise

Job description

PFMEA Manufacturing Engineer - (NO C2C OR THIRD PARTY)

PFMEA Manufacturing Engineer - (NO C2C OR THIRD PARTY)

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PFMEA Manufacturing Engineer - (NO C2C OR THIRD PARTY)

Location: Onsite – Batesville, Indiana (47006)

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

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 [e-mail].

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

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

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Contract

Job function

• Job function

  Engineering, Manufacturing, and Production

• Industries

  Pharmaceutical Manufacturing, Medical Equipment Manufacturing, and Manufacturing

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Inferred from the description for this job

Medical insurance

Vision insurance

401(k)

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