Senior Manufacturing Engineer

Enterprise EQ; Cambridge (MA); On-site; USD 89,544; Full time

Job summary

A leading medical device company is seeking a Senior Manufacturing Engineer in Cambridge, MA. The role involves improving manufacturing processes and ensuring efficiency in design transfer and production validation. Candidates should have at least 5 years of experience in medical device manufacturing and proficiency in SolidWorks. This is a 5-month contract position with a pay rate of $65/hr, excluding benefits.

Qualifications

• 5+ years of experience in Medical Device Manufacturing Engineering.
• Experience in new product development and validating processes.
• Proficient in modeling and drawing with SolidWorks.

Responsibilities

• Develop and optimize efficient manufacturing processes for medical devices.
• Produce production-level assembly and part drawings.
• Incorporate DFM, Six Sigma, and LEAN principles into designs.

Skills

Medical Device Manufacturing Engineering

SolidWorks

Design transfer

Process validation

Six Sigma

LEAN principles

Education

Bachelors Degree in Mechanical Engineering

Job description

Cambridge, MA, United States Confidential

About the job Senior Manufacturing Engineer

Hello,

• Client: Manufacturing Industry
• Position: Medical Device Senior Manufacturing Engineer
• Location: Cambridge, MA 02139
• Duration: 05 Months Contract on W2 basis

Max Pay Rate - $65/hr on W2 - With No Benefits

MUST HAVE:

• Education: Bachelors Degree or higher in Mechanical Engineering.
• 5+ years of experience in Medical Device Manufacturing Engineering, including at least three years in new product development, design transfer to production, and validating processes.
• Excellent modeling and drawing skills using SolidWorks, including proficiency with assemblies that contain dozens of parts.
• Experience working with contract manufacturers/vendors for capital equipment, electronics testing, and/or catheter manufacturing is strongly preferred.
• Proven track record in design transfer, process validation, and knowledge of sterilizable polymers and catheter fabrication techniques.

Key Responsibilities (Do) :

• Developed and optimized efficient, cost-effective, and validated manufacturing processes for medical devices, focusing on capital and/or disposable devices, including assembly, lot release testing, sterilization, and packaging.
• Produce production-level assembly and part drawings for all components and sub-assemblies.
• Incorporate Design for Manufacturing (DFM), Six Sigma, and LEAN principles into product and process designs to ensure manufacturability, minimize costs, and achieve optimal production efficiency through activities like DFMA reviews and cycle time optimization.
• Proactively identify and evaluate potential contract manufacturing partners by analyzing quality, cost, delivery timelines, and regulatory compliance capabilities to recommend optimal providers.
• Lead and collaborate with contract manufacturers in selecting and developing the most efficient and reliable manufacturing processes and sites while fostering strong partnerships.