Manufacturing Technician I, Medical Devices Resume

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Manufacturing Technician I, Medical Devices Resume Ella Martin Manufacturing Technician I, Medical Devices (408) 555-2637 ella.martin@example.com linkedin.com/example/ellamartin San Jose, CA 95112 STRENGTHS Controlled Assembly Built repeat training modules from clear instructions, then checked each connection before moving forward. Quality Documentation Recorded build and test details through GDP practices. Clear entries made review easier for instructors. Practical Testing Used multimeters, calipers, presses, and torque tools during checks. Hands on results guided next steps. Issue Escalation Paused after an out of tolerance reading, documented findings, and brought the issue forward promptly. Production Readiness Reviewed line clearance, calibration status, materials, and workstation order before starting each build. SKILLS Electro Mechanical Assembly Medical Device Manufacturing Robotics Cable Harnesses Torque Wrenches Calipers Multimeters Presses Functional Testing Good Documentation Practices ISO 13485 FDA QSR ESD Protection Contamination Control 6S LANGUAGES English Native 40 Spanish Intermediate 20 MY CAREER 1.4 Years Electromechanical Medical Device Assembly Lab Technician at Student Lab (9 Months) Robotic Module Manufacturing Capstone Technician at Capstone Project (4 Months) Regulated Manufacturing Systems Project Technician at Course Project (4 Months) SUMMARY Early career manufacturing technician completing an Associate of Science in Mechatronics, with supervised lab experience building electromechanical medical device training modules. Practical work includes robotic joints , cable harnesses, control enclosures, mechanical parts , torque controlled fastening, multimeter testing, caliper checks, presses, ESD protection, contamination control, 6S, line clearance, and calibration status review. Academic projects applied controlled work instructions , engineering drawings, ISO 13485 concepts, FDA QSR concepts, Good Documentation Practices , electronic DHR entries, MES workflows, SAP fundamentals, material transactions, cycle counts, and WIP tracking. Careful documentation and steady troubleshooting supported safe escalation of nonconforming conditions. Ready for structured production work, flexible scheduling, and continued certification on designated medical device modules. EDUCATION Associate of Science in Mechatronics San Jose City College GPA: 4.0 2027 San Jose, California Coursework: Electromechanical Assembly, Medical Device Manufacturing, Robotics, Quality Systems, Manufacturing Documentation TECHNICAL SKILLS Assembly Tools: Torque wrenches, screwdrivers, calipers Electrical Testing: Multimeters, continuity testing, functional testing Production Systems: MES, ERP, SAP Quality Standards: ISO 13485, FDA QSR, quality standards Documentation: Good Documentation Practices, electronic DHR, controlled forms Workplace Controls: ESD protection, contamination control, clean manufacturing Material Control: Raw materials, sub assemblies, WIP Inventory Operations: Material transactions, cycle counts, shortage reporting Production Readiness: Line clearance, calibration status, maintenance verification Workstation Methods: 6S, organized work areas, process clarification Mechanical Equipment: Presses, fasteners, mechanical parts Robotic Systems: Robotic joints, control modules, cable harnesses Inspection Methods: In process inspection, acceptance criteria, quality checks Training Systems: ComplianceWire, training records, module certification Safety Practices: Safety requirements, overtime readiness, weekend scheduling SKILLS Electro Mechanical Assembly Medical Device Manufacturing Robotics Cable Harnesses Torque Wrenches Calipers Multimeters Presses Functional Testing Good Documentation Practices ISO 13485 FDA QSR ESD Protection Contamination Control 6S EXPERIENCE Electromechanical Medical Device Assembly Lab Technician Student Lab January 2026 - Present San Jose, California Support supervised training builds for electromechanical medical device modules, following controlled work instructions, inspection criteria, safety practices, and documentation expectations. Work covers robotic joints, cable harnesses, control enclosures, verification tools, ESD controls, clean manufacturing, and electronic records. Built robotic joints and cable harnesses from controlled work instructions during supervised module assembly. Used torque wrenches , calipers, presses, and multimeters for functional and mechanical verification . Applied ESD protection , clean manufacturing , contamination control, and 6S during repeat laboratory builds. Recorded build, inspection, and test results in simulated electronic DHR records using GDP. Checked calibration status and line clearance before escalating out of tolerance readings. Completed repeat robotic joint builds and demonstrated module proficiency through functional checks. Robotic Module Manufacturing Capstone Technician Capstone Project August 2025 - December 2025 San Jose, California Completed supervised capstone manufacturing work for an electromechanical robotic module, using engineering drawings, assembly procedures, inspection planning, training inventory records, and structured issue escalation. Focus included cable routing, connectors, functional testing, quality records, and material control. Created a supervised robotic module build plan from engineering drawings and assembly procedures. Assembled cable routing, mechanical joints, connectors, and fasteners with torque controlled tools. Performed continuity and functional tests, then documented prototype results against acceptance criteria. Created an in process inspection checklist using ISO 13485 and FDA QSR coursework. Logged raw materials , sub assemblies , and WIP in training ERP and SAP records. Investigated connector test failure through visual inspection and multimeter checks before escalation. Regulated Manufacturing Systems Project Technician Course Project January 2025 - May 2025 San Jose, California Completed a supervised production exercise covering line setup, material readiness, controlled documentation, quality verification, training MES records, SAP inventory comparisons, cycle counts, and escalation decisions. Work simulated a regulated medical device manufacturing environment. Completed simulated line setup with material readiness , documentation, and quality verification steps. Recorded routing and inspection status in training MES , then compared SAP inventory data. Performed raw material, sub assembly, and WIP cycle counts and documented discrepancies. Applied Good Documentation Practices to controlled forms through supervised peer review. Mapped a 6S workstation layout with ESD controls and calibrated measurement equipment. Reviewed quality holds and calibration status scenarios before selecting escalation paths. PROJECTS Robotic Module Manufacturing Capstone 2025 Built and evaluated a supervised robotic module using engineering drawings, torque controlled assembly, continuity testing, inspection planning, and training inventory records. Project centered on clear documentation and safe issue escalation. Regulated Manufacturing Systems Simulation 2025 Modeled a medical device production line with MES records, SAP inventory comparisons, cycle counts, line clearance, material readiness, ESD controls, and quality hold decisions. LEADERSHIP & AWARDS Dean’s List, San Jose City College, 2025 Technical Education Achievement Scholarship, San Jose City College, 2026 Capstone Documentation Excellence Recognition, 2025 CERTIFICATIONS Introduction to SAP Concepts for Manufacturing 2026 ESD and Electronics Assembly Fundamentals 2026 PROFESSIONAL AFFILIATIONS Peer Mentor, Mechatronics Student Lab, 2026 Member, Campus Robotics Project Group, 2025 to 2026 Volunteer, College Manufacturing Lab Open House, 2025 LANGUAGES English (Native) Spanish (Intermediate) ADDITIONAL INFORMATION Work Status : Authorized to work in United States. No sponsorship required. ADDITIONAL INFORMATION Work Status : Authorized to work in United States. No sponsorship required. REFERENCES AVAILABLE ON REQUEST

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