Jobs at Vantedge Medical

Lead planning, purchasing, and logistics across three California sites. Build supply chain processes and MRP best practices, drive production scheduling, capacity planning, inventory reduction, strategic sourcing, supplier performance, warehouse optimization, and talent development. Act as primary customer communicator and collaborate with corporate COE on S&OP and analytics to improve supply chain maturity.

Lead facility-wide lean transformation by planning and facilitating kaizen events, training and mentoring staff, implementing VOS/lean tools, tracking KPIs and cost savings, and supporting new product introductions and process improvements to drive quality, flow, and sustained operational gains.

Support accounts payable, accounts receivable, and billing tasks: process vendor invoices and payments, record customer payments, prepare invoices, assist reconciliations, month-end close, basic journal entries, audit preparation, and general accounting file maintenance.

Lead process development and continuous improvement for large-format steel and medical device manufacturing. Develop tooling/fixtures, implement lean methods, perform root cause analysis, manage CAPAs, create standard work and validation protocols, support new product launches, quote new business, and collaborate cross-functionally to improve quality, cost, delivery and safety.

Coordinate MRB dispositions and RMA processing: update NCRs, manage rework/scrap/RTS/UAI workflows, maintain MRB log, support QC inspections, and communicate with Engineering, Manufacturing, and Quality to resolve production issues and ensure timely customer returns.

Seeking a Senior Manufacturing Engineer to lead process development and cost management in medical device manufacturing, ensuring quality and efficiency.

Support process development and improvement for machining and metals production at a medical device contract manufacturer. Develop tooling/fixtures, apply root-cause analysis, ensure validation and compliance, support new product launches, drive lean improvements, and collaborate cross-functionally to meet quality, cost, capacity, and delivery goals.

Lead process development and improvement for sheet metal and welding manufacturing at a medical device contract manufacturer. Develop tooling/fixtures, validate processes, apply lean and root-cause analysis to improve quality, cost, delivery, and capacity. Support new product launches, tech transfers, CAPAs, and collaborate with quality, regulatory, customers, and cross-functional teams to implement scalable, compliant production solutions.

Lead full-cycle recruiting for manufacturing, technical, and professional roles while providing broad HR generalist support: employee relations, performance management, onboarding, HRIS maintenance, benefits support, compliance with CA employment laws, training, and HR process improvements.

Develops and delivers shop-floor and safety training for manufacturing employees, creates training materials and calendars, evaluates skill gaps, administers the site LMS, conducts safety inspections and audits, implements safety procedures, and maintains safety documentation and SDS access.

Lead development and implementation of economical, validated manufacturing processes for medical device components. Manage projects, resolve manufacturing issues, drive cost/quality/productivity improvements, coordinate validation and quality activities, mentor engineers, and lead continuous improvement efforts while maintaining documentation and customer communication.

Support product and process quality for sheet metal manufacturing: analyze quality data, lead corrective actions, drive supplier quality, manage NCMR and complaints, maintain ISO 9001/13485 QMS, lead APQP/PPAP and validations (IQ/OQ/PQ), author SOPs, and implement continuous improvement using statistical tools.

Oversee the Sheet Metal department, manage production, quality, and operational excellence initiatives for improved efficiency, and ensure customer satisfaction.

The Continuous Improvement Engineer will drive efficiency and quality enhancements in manufacturing through Lean and Six Sigma methodologies, while mentoring staff and ensuring regulatory compliance.

Lead process development and continuous improvement for PECM/ECF and precision manufacturing. Develop, validate, and implement robust production processes, tooling, and documentation. Manage NPI, root cause investigations, CAPAs, and cross-functional projects to improve quality, cost, delivery, and capacity in a regulated medical-device contract manufacturing environment.

The Engineering Manager oversees plant engineering execution, ensuring reliability in sheet metal fabrication. Responsibilities include leading engineering teams, process improvements, maintenance strategies, and equipment readiness while partnering with production and quality teams.

Lead process development, NPI launch readiness, and continuous improvement for medical device contract manufacturing. Create routings, fixtures, validations, and work instructions; execute MRB/CAPA/ECO activities; ensure FDA/ISO compliance and collaborate with customers and suppliers to improve quality, cost, delivery, and safety.