Process /Manufacturing Engineer - US Citizen / Green Card Holder

Fusion Life Sciences Technologies (www.fusionlifesolutions.com ) is a WBE-certified Healthcare Staffing and Engineering Services provider supporting industries including Pharma, Medical Devices, Aeronautical, Supply Chain, Heavy/Light Industrial, Food & Beverage, and Automotive. We proudly partner with 120+ clients such as Johnson & Johnson, Haemonetics, Delta, Caterpillar, Artisan Chef, Baxter, and many more. Our wide network of consultants and contract-to-hire engineers brings deep expertise across Engineering, Technical, Administrative, Healthcare, Life Sciences, Blue Collar, Skilled Trades, IT, Software Development, Manufacturing, and Supply Chain sectors. What sets us apart is our AI-powered, in-house software's enabling us to source and screen top talent within hours. This ensures rapid response times, high-quality matches, and virtually zero attrition.

Job Title : Process Engineer - Medical Device Industry

Location : Cincinnati, OH (Onsite)

Duration : 12 Months

Need US Citizens for this opportunity

Travel to Mexico / Ireland / Singapore



Overview

Seeking a Contract Process Engineer to support the design, development, optimization, and scale-up of

manufacturing processes for medical device and drug-delivery components. The contractor will work

with cross-functional teams and suppliers to deliver robust, manufacturable solutions.

Key Responsibilities

• Develop, optimize, and validate component and assembly manufacturing processes.
• Support DFM/A activities and translate product requirements into process outputs.
• Conduct process characterization, capability studies, and statistical analyses.
• Partner with R&D, Quality, Regulatory, Supplier Engineering, and Operations throughout development.
• Support equipment debug, characterization, FAT, and qualification activities.
• Troubleshoot manufacturing and compliance issues and support process transfer to production sites.

Preferred Background

• 6+ years in process development within a regulated industry.
• Strong understanding of component fabrication and assembly processes.
• Experience with DFMA, FMEA, and applied statistics (MSA, process capability).
• Experience with equipment commissioning (debug, characterization, FAT, validation).
• Familiarity with Lean, Six Sigma, or similar methodologies.
• Experience supporting commercialization or working with global teams/suppliers.
• Prior J&J or MedTech experience is strongly preferred.

All your information will be kept confidential according to EEO guidelines.