Jessica Campos

• Inspects electronic or mechanical assemblies, subassemblies, and parts for compliance with acceptance criteria as defined by specifications, drawings, samples, or illustrations
• Inspects or tests components and raw material according to written inspection procedures
• Examines units visually, with microscope or another magnifying device, to determine physical defects according to written inspection procedures
• Compares assemblies with drawings, parts lists, illustrations, and/or samples to verify conformance and detect assembly errors
• Examines alignment of parts and verifies installation of hardware on assemblies and subassemblies
• Measures parts for conformance to specified dimensions using measuring instruments or equipment
• Accepts or rejects materials/products inspected based on conformance to acceptance criteria
• Records inspection data on appropriate forms, logs, and/or in computer databases
• Maintains controlled document files and test records in a timely and accurate manner
• Coordinates calibration of all test equipment and fixtures
• Monitors, critical equipment, and instrumentation to ensure proper operation and calibration
• Identifies and controls non-conforming material and defective products until material has been quarantined
• Identified and evaluated quality-related problems, initiating corrective actions and preventive measures.
• Managed identification and control of nonconforming materials and defective products through effective segregation and labeling.
• Monitored performance and generated reports detailing quality of products and defect rates.
• Developed and implemented best practices to enhance operational efficiency and minimize defect rates.
• Communicated with production team members about quality issues.
• Executed visual inspections and non-destructive tests on products.
• Completed precise measurements using special tools.
• Used Microvu to inspect quality of products, taking note of functionality, appearance, and other specifications.
• Used hand tools, instruments, gauges, and equipment to complete accurate measurements and noted results for official records.
• Evaluated items to assign grades and marked quality level, rejection status, or acceptance.
• Created and deployed best practices to improve efficiency and reduce defects

Audited device history records for completeness before product release.
Created certificates for product receipt in various markets.
Indexed and stored quality records for efficient access.
Retrieved records promptly upon request to support operations.
Coordinated with departments to rectify documentation errors.
Collaborated with the traceability team and management on key performance indicators.
Provided feedback on processes as part of business monitoring efforts.

• Optimized traceability by developing organizational filing systems for confidential employee records and reports, improving retrieval efficiency.
• Recorded lot numbers and serial numbers in ERP system, enhancing traceability for produced items.
• Audited device history records for completeness before product release.Created certificates for product receipt in various markets.Indexed and stored quality records for efficient access.Retrieved records promptly upon request to support operations.Coordinated with departments to rectify documentation errors.Collaborated with the traceability team and management on key performance indicators.Provided feedback on processes as part of business monitoring efforts.

• Conducted thorough inspections of medical devices to ensure quality compliance.
• Utilized precision measuring instruments for accurate assessment of product specifications.
• Documented inspection results through detailed reports and data summaries in quality database, ensuring traceability and compliance.
• Developed and implemented inspection procedures that streamlined workflows and ensured adherence to quality standards.
• Reviewed non-conformance reports to identify corrective actions, contributing to continuous improvement in quality control processes.
• Manufactured over 25 lifesparc controllers daily, adhering to stringent specifications.
• Executed stock transactions using QAD software for efficient inventory management.
• Participated in audits to ensure compliance with applicable regulations and standards.

• Developed and implemented compliant, cost-effective quality system ensuring product and service reliability, safety, and effectiveness
• Analyzed test data to assess material performance and reliability, informing quality assurance decisions
• Conducted hazard analyses, identified critical control points, and established critical limits in developing quality assurance plans
• Followed Standard Operating Procedures (SOPs) and executed Good Manufacturing Practices (GMPs) in compliance with Regulatory requirements
• Executed ampoulization, assembly, packaging, and sterilization processes for products in Yoshida Tango Project - Phase 1A Stability Study.
• Completed assembly tasks for Aphrodite 3mL applicators, ensuring readiness for Frontier Clinical Supplies.
• Creation of manufacturing procedures, manufacturing instructions and batch records for A&W wipes.
• Configured different sized ampoule cassettes on specific racks and placed probes and test samples in designated locations during research activities for cascading water system (CWS)
• Supervised use of electric pallet jack to load and unload racks in manufacturing environment

• Inspected final device assemblies per established procedures as Quality Control Inspector.
• Manufactured and assembled medical devices used in VNS Therapy per established procedures
• Led training sessions for manufacturing operators in Costa Rica facility, enhancing team capabilities and operational efficiency.
• Trained personnel at US and Costa Rica facilities, ensuring compliance with regulatory requirements.
• Executed stock transactions in QAD software for all production line materials, maintaining accurate inventory records.