Manufacturing Test Technician
Vantage MedTech
Summary
Vantage MedTech provides comprehensive design and manufacturing services, supporting the advancement of medical technologies from concept through to product realization. As a hands-on technical expert, you will help build and test innovative medical devices, ensuring the quality, reliability, and performance of electronic assemblies and devices.
Job description
Key Responsibilities
- Execute Acceptance Test Procedures (ATPs), Functional Test Procedures (FTPs), and production validation testing.
- Perform functional, electrical, and performance testing of assemblies, subassemblies, and finished products.
- Troubleshoot test failures and manufacturing issues to support production throughput and quality objectives.
- Support engineering builds, pilot runs, and new product introductions (NPI).
- Collect, document, and analyze failure data to identify trends and support root cause investigations.
- Support Quality and Engineering investigations through detailed technical documentation and product evaluation.
- Assist in the development, validation, and continuous improvement of test methods, fixtures, work instructions, and manufacturing processes.
- Operate electronic test equipment including oscilloscopes, multimeters, power supplies, signal generators, and custom test fixtures.
- Read and interpret schematics, assembly drawings, wiring diagrams, and technical documentation.
- Verify calibration status of test equipment prior to use.
- Perform board-level soldering, rework, component replacement, and repair activities.
- Evaluate, troubleshoot, repair, and document customer returned products in accordance with approved service procedures.
- Generate accurate manufacturing, service, and quality records within ERP and quality systems.
- Identify, document, and report nonconformances and support corrective and preventive action activities.
- Support onboarding and training of new technicians.
- Collaborate with Manufacturing, Quality, Engineering, and Service teams to improve product reliability, manufacturability, and process efficiency.
- Follow all safety, ESD, quality system, and regulatory requirements.
Education and Experience
- Associate degree in Electronics Technology, Electrical Engineering Technology, or related field preferred; equivalent technical training and experience considered.
- Minimum 2 years of experience in electronics testing, manufacturing testing, troubleshooting, or production support.
- Strong understanding of electronic components, circuits, diagnostics, and manufacturing test practices.
- Experience using oscilloscopes, multimeters, power supplies, signal generators, and related test equipment.
- Ability to read and interpret schematics, assembly drawings, test procedures, and technical documentation.
- Familiarity with firmware loading, device configuration, serial communications, and software-based diagnostic tools.
- Proficiency with Microsoft Office applications, ERP, and electronic quality systems.
- Strong troubleshooting, analytical, communication, and documentation skills.
- Ability to work independently with limited supervision.
Preferred Qualifications
- Experience in medical device manufacturing or another regulated industry.
- Experience supporting design verification or validation testing.
- Familiarity with FDA Quality Management System Regulation (QMSR), 21 CFR Part 820, and ISO 13485.
- IPC-A-610, IPC J-STD-001, or equivalent electronics manufacturing certifications.
- Experience supporting process validation, failure analysis, CAPA activities, and continuous improvement initiatives.
- Knowledge of Lean Manufacturing principles.
Requirements
- Associate degree in Electronics Technology, Electrical Engineering Technology, or related field preferred; equivalent technical training and experience considered
- Minimum 2 years of experience in electronics testing, manufacturing testing, troubleshooting, or production support
- Strong understanding of electronic components, circuits, diagnostics, and manufacturing test practices
- Experience using oscilloscopes, multimeters, power supplies, signal generators, and related test equipment
- Ability to read and interpret schematics, assembly drawings, test procedures, and technical documentation
- Familiarity with firmware loading, device configuration, serial communications, and software-based diagnostic tools
- Proficiency with Microsoft Office applications, ERP, and electronic quality systems
- Strong troubleshooting, analytical, communication, and documentation skills
- Ability to work independently with limited supervision
- Experience in medical device manufacturing or another regulated industry
- Experience supporting design verification or validation testing
- Familiarity with FDA Quality Management System Regulation (QMSR), 21 CFR Part 820, and ISO 13485
- IPC-A-610, IPC J-STD-001, or equivalent electronics manufacturing certifications
- Experience supporting process validation, failure analysis, CAPA activities, and continuous improvement initiatives
- Knowledge of Lean Manufacturing principles
Benefits
- Health, Vision & Dental Insurance
- Generous Paid Time Off
- Retirement Plan with Matching
Company overview
Vantage MedTech is a leading contract development and manufacturing organization (CDMO) specializing in comprehensive medical device solutions from concept through product realization. Formed through the merger of Sterling Medical Devices and RBC Medical Innovations, the company provides end-to-end services including feasibility studies, product development, prototyping, clinical and commercial manufacturing, and after-market support. With over 150+ medical device engineers and decades of industry expertise, Vantage MedTech partners with both innovative MedTech startups and established large medical device companies to accelerate development timelines and minimize regulatory risks. The company's proprietary Advantage Platforms® leverage established software and hardware architectures to reduce development timelines by up to 60% while maintaining rigorous verification and validation standards. Operating from FDA-registered facilities in New Jersey and Kansas, Vantage MedTech offers flexible manufacturing capabilities that scale from small-quantity clinical builds to full commercial production, supporting the entire product lifecycle with ISO 13485 certified excellence.