Manufacturing Engineer

Manufacturing Engineer at Stevenson Search Partners Manufacturing Engineer at Stevenson Search Partners in Vineburg, California Posted in 1 day ago.

Type:

full-time

Job Description:

Our On-Demand Talent Solutions team is seeking a Manufacturing Engineer to join our highly valued client. The ideal candidate combines strong mechanical design skills with hands-on manufacturing experience and a solid understanding of regulated environments. •South Bay Area Only•Client requires direct W-2 employment; Corp-to-Corp arrangements are not permitted for this role.•

Summary:

As a Manufacturing Engineer you will contribute to product design through DFM work and collaborate closely with R D Engineers, factories and external partners, as needed.

Responsibilities:

Design, develop, and release custom fixtures, assembly aids and inspection/test methods to support verification, and manufacturing of medical devices. Create detailed CAD models and fabrication drawings while collaborating with suppliers and contract manufacturers to ensure manufacturability, durability, cost-effectiveness, and successful production deployment. Provide on-site and remote support for equipment bring-up, debugging, process stabilization, and root cause analysis while driving DFM/DFA improvements and corrective actions for tooling and process-related issues. Develop and execute

IQ/OQ/PQ

validation protocols, analyze validation data, implement process improvements, and author documentation in compliance with FDA and ISO standards (e.g.

ISO13485

). Partner cross-functionally with R D, Quality, and Supplier Quality teams to support design transfer readiness, technical reviews, and quality systems documentation including BOMs, DMRs, Routers, Manufacturing Instructions, FMEAs, and ECOs.

Qualifications:

Bachelor's degree in Mechanical Engineering or related field. 4-7+ years of experience in manufacturing engineering, tooling, or fixture design. Experience with catheters is desirable. Strong CAD experience (e.g., SolidWorks) and hands-on expertise in tooling and process validation (IQ/OQ/PQ). Working knowledge of

ISO 13485, 21 CFR

Part 820, and statistical methodologies including DOE and process capability analysis.