Mechanical Project Engineer-Medical Device Address is: Hybrid role - 3 days onsite and 2 remote. Days onsite will be 3 days between Mon - Thurs. During training, this person will need to be onsite when the engineers will be there. Notes from the manager: Medical Device or Regulated Device experience required. CAPA experience required. Trackwise and SAP experience highly desired. Job Responsibilities: The Mechanical Project Development Engineer is responsible for designing and developing comple

Job Summary: The Mechanical Project Development Engineer is responsible for designing and developing complex medical device components by translating engineering requirements into high-quality, compliant design solutions with limited supervision. This role defines and executes test and validation activities, resolves advanced technical issues to ensure reliable production, and evaluates external components and technologies to meet quality, performance, and regulatory standards. Roles & Responsib

Job Title: System Engineer Duration: 12 Months Location: New Kensington, PA (Hybrid 3 days onsite) Position Overview We are seeking a hands-on Systems Engineer with direct medical device new product development experience who has served as a primary systems lead not solely in a quality or support capacity. The ideal candidate will be a broad technical systems thinker with demonstrated ownership of system architecture, risk management, and standards compliance throughout the full product lifecycl

Job Title: Verification & Validation (V&V) Engineer Medical DevicesLocation: Indianola, PA (Onsite)Engagement Type: ContractExperience: 8 12 Years Work Mode: Onsite Product Testing Lab / Client Location Job SummaryWe are seeking an experienced Verification & Validation (V&V) Engineer to support testing, compliance, and certification of medical device products. This role requires hands-on hardware validation, coordination with external certification labs, and close collaboration with hardware, so