Sylvia J Figueroa

• Responsible for all endoscopes returned to the facility for service and/or repair. Performs initial inspection, defines the necessary repairs and lists the parts and components needed to complete the repair process. Works on all models of Loaner/Demo and Customer scopes.
• Performs initial inspection, defines the necessary repairs and lists the parts and components needed to complete the repair process.
• Provides input and guidance on technical issues.
• I am qualified to read and understand schematic drawings and wiring diagrams and/or with mechanical drawings and assembly procedures.
• Assemble and disassemble small highly delicate parts of the endoscope assuring the unit meets the established specifications.
• Performs final quality inspection on the completed repair to ensure the product is up to the manufacturer's original specifications before passing the scope along to the final quality control station.
• Troubleshoot potential problems not originally discovered during the initial inspection.

• Responsible for production inspection following cGMP criteria for both cosmetics and OTC drug products.
• Responsible for the training of multiple line inspectors following cGMP regulations specifically regarding weights and measurements, label, and code placement.
• Specifically regarding weights and measurements, label, and code placement.
• Managed documentation for line inspectors, micro testing, retains and training.
• Worked directly with the regulatory director to implement new policies and inspection requirements.
• Followed strict document control procedures for the retain of inspection records including back-up file production of critical inspection records including tracking of microbiological and analytical testing requirements.

• Responsible for conducting 100% visual inspection, and test receiving, in-process and finished products.
• Identify and record any problems relating to the product, process and quality system.
• Maintain quality control equipment and calibration, measuring and test equipment to
• Execute all Infor System quality records in accordance with documented procedures.
• Knowledgeable in Product Disposition and Rework Activities.
• Use of calipers to make sure that the measuring of the product is correct according to company standards. And other tools depending on the assigned inspection such as scissors and forceps sterilized.
• Clean Room Inspector Experience in Medical Device Environment.

Working in an impressive variety of settings, responsible for maintaining quality-assurance processes, testing products, and recording and analyzing results data during product development and manufacturing.

• Assist Endoscope Repair Technician when necessary.
• Checks and tests on incoming endoscopes requiring repair and outgoing that already has been repaired.
• Perform appropriate data entry, data updates and research.
• Electro-mechanical disassembly and proper use of microscope.
• Perform inspection in accordance with SOPs and internal quality policies.
• Experience in Electronic, mechanical and soldering skills.

• Photocopying, balancing activities, data entry and encoding of deposits, generation of reports and statements.
• Process invoices resolve payments issues, sorting of incoming work, mailing material to customers and operating departmental machines.
• (Opex 50/51), Mail sorter Machine, NCR 7780, Scanning Images 3600 Machine. (Special handling, account Lookup).
• Increased number and quality of search results with database search techniques
• Filed electronic and hard copy documents to maintain organized records
• Maintained [Type] database for accurate and updated information

• Established open and professional relationships with team members to achieve quick resolutions for various issues.
• Monitored team performance and provided constructive feedback to increase productivity and maintain quality standards.
• Maintained overall safe work environment with employee training programs and enforcement of safety procedures.
• Monitoring used machines and process variables, taking corrective action as required and promptly reporting conditions negatively impacting quality, output, or equipment performance.
• Completion and delivery of finished piece parts to the specified quality levels on a timely basis.
• Equipment set-up and performance of related first piece inspection to insure achievement of desired quality levels.
• Interface with electronic quality, production and documentation systems providing accurate information.
• Performance of ongoing quality checks, recording of requested data and timely reporting of discrepancies.
• Followed strict document control procedures for the retain of inspection records including back-up file production of critical inspection records including tracking of microbiological and analytical testing requirements.
• Comply with EHS regulations and police.