Skip to main content
Tallo logoTallo logo

Manufacturing Engineer

Job

Stevenson Search Partners

Remote

Full-Time

Posted 2 weeks ago (Updated 2 days ago) • Actively hiring

Expires 6/28/2026

Apply for this opportunity

This job application is on an outside website. Be sure to review the job posting there to verify it's the same.

Review key factors to help you decide if the role fits your goals.
How is this calculated?
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
80
out of 100
Average of individual scores

Were these scores useful?

Skill Insights

Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.

Job Description

Manufacturing Engineer at Stevenson Search Partners Manufacturing Engineer at Stevenson Search Partners in Piedmont, California Posted in 11 days 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.