Process /Manufacturing Engineer - Medical Device Industry at Techtrueup

Cincinnati, Ohio, United States -

Full Time

Start Date

Immediate

Expiry Date

14 May, 26

Salary

0.0

Posted On

13 Feb, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Process Development, Manufacturing Processes, Medical Device, DFM/A, Process Characterization, Capability Studies, Statistical Analysis, Equipment Debug, FAT, Process Transfer, FMEA, MSA, Lean, Six Sigma, Commercialization, Supplier Engineering

Industry

Human Resources Services

Description

Company Description 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 Description Job Title : Process Engineer - Medical Device Industry. Location : Cincinnati, OH (Onsite) Duration : 12 Months Need US Citizens for this opportunity. 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. Travel to Mexico / Ireland Additional Information All your information will be kept confidential according to EEO guidelines.

Responsibilities

The contractor will be responsible for developing, optimizing, and validating manufacturing processes for medical device and drug-delivery components, working with cross-functional teams to ensure robust and manufacturable solutions. Key tasks include supporting Design for Manufacturing/Assembly (DFM/A), conducting process characterization and capability studies, and troubleshooting manufacturing issues.