Manufacturing Engineer - SolidWorks and PLM Lead (Onsite)

Akkodis; Madison (WI); On-site; USD 55,000 - 62,000; Full time

Benefits offered by this job

401K plan

Medical insurance

Dental insurance

Vision care

Short-term disability

EAP program

Commuter benefits

Job summary

Akkodis is seeking a Manufacturing Engineer for a 12-month onsite contract in Madison, WI 53719. You will design with SolidWorks, create assemblies with BOMs, and generate GD&T drawings to support product lifecycle management.

Ideal candidates have a engineering degree with 2+ years of experience and can drive projects to completion while collaborating with vendors and QA/compliance teams to meet FDA/GMP/ISO standards.

Qualifications

• Bachelor’s degree in engineering or equivalent with relevant experience.
• SolidWorks design and drawing creation experience required.
• Experience driving projects to completion.
• Knowledge of FDA, GMP, ISO, CAP, CLIA requirements is a plus.

Responsibilities

• Create SolidWorks designs and drawings for new and existing products.
• Create assembly files with a complete BOM.
• Create drawings with tolerances, including GD&T.
• Support the PLM Vault system and product lifecycle management.
• Develop assembly procedures for new or modified designs.
• Coordinate with external vendors to quote and order prototype parts.
• Support assembly, testing, and documentation of designs.
• Lead or support design reviews and first article inspections.
• Ensure documentation complies with FDA, GMP, ISO, CAP, CLIA requirements.

Skills

Project management

Problem solving

Education

Bachelor's degree in Engineering

Associate degree in Engineering/Technology

Tools

Solidworks

BOM management

Job description

Akkodis is seeking a Manufacturing Engineer for a 12-month onsite contract in Madison, WI 53719. You will design with SolidWorks, create assemblies with BOMs, and generate GD&T drawings to support product lifecycle management.

Ideal candidates have a engineering degree with 2+ years of experience and can drive projects to completion while collaborating with vendors and QA/compliance teams to meet FDA/GMP/ISO standards.