● Oversee and manage field staff, including technicians, contractors, and other field personnel.Ensure they are adequately trained and equipped to perform their duties effectively.● Plan, organize, and monitor field projects to ensure they are completed on time, within budget, andin compliance with quality and safety standards.● Allocate resources such as equipment, materials, and manpower to meet project requirementsefficiently.● Maintain and enforce quality control standards to ensure that work performed in the field meets orexceeds established quality benchmarks.● Promote and enforce safety protocols and regulations to minimize risks and ensure the safety offield personnel and the public.● Serve as the primary point of contact between the field teams and clients or stakeholders.Communicate project progress, address concerns, and provide updates as necessary.● Assist in budget preparation and monitor expenses related to field operations. Identify cost-savingopportunities and implement strategies to optimize spending.● Gather field data, generate reports, and maintain accurate records of activities, expenses, andproject milestones.● Identify and resolve issues or obstacles that arise during field operations to ensure projects stay ontrack.● Provide training and guidance to field personnel to enhance their skills and knowledge.

• Responsible for maintaining and monitoring equipment and collection of test data in support of environmental monitoring support. • Support the implementation of inspection tools and methods as well as Test Method Validations and Gage R&R's and supporting component verification activities.• Performs analyses, inspection, and tests of, packaging materials, quantitative assays on samples, and/or finished products from manufacturing, to ensure quality standards and compliance to customer and regulatory requirements, and tolerance specifications for the chemical or physical property. Conduct Compliance Audits as assigned.• Performs a variety of qualitative tests or qualitative assays on samples, and to aid in maintenance and certification of test instruments and apparatus to ensure compliance.• Performs required inspections, checks, analysis and documentation of studies.• Prepares and monitors quality statistics and reports.• Reviews production records for conformance to procedures.• Manage non-conformance matrix and conducts non-conformance tests of manufactured, packaged or tested product.• Prepare and maintain the Change Order (CO) and Change Request (CR). Work in issuing, tracking maintaining and identifying CAPA as per (NCMR's). Prepare and write validation protocols for product and processes (IQ, OQ and PQ). • Develops quality assurance plans by conducting hazard analyses; identifying critical control points and preventive measures; establishing critical limits, monitoring procedures, corrective actions, and verification procedures; monitoring inventories. Support and train Quality Inspectors supporting production line. Assist in implemented Corrective and Preventative Actions.• Prepares quality documentation and reports by collecting, analyzing and summarizing information and trends including failed processes, stability studies, recalls, corrective actions, and re-validations.

Maintaining / Monitoring equipment and collection of test data in support of product verification and reliability testing activities.Documentation of test data results and participates in failure analysisinvestigation.Support process validation activities.Support product qualification and component verification activities.Support the implementation of inspection tools and methodsPerform product inspectionsDocument non-conformances per established SOPs.Review of Device History Record (DHR) documentation for discrepancies / missing information.Assist in the resolution of non-conformances.Assist in implemented Corrective and Preventative Actions.Conduct Compliance Audits as assigned.Execute and document testing in support of QA Engineering

Produce and read testing programs to assess and change product performances and consistency for maker of business Audio equipmentProvide written reports on experiment results, suggesting modifications to designs, manufacturing, or market problems in productHelp in implementation of the new projects including the parts numbering systems and the project scheduling precedence systemGather and arrange information for the production test analysis and manufactoring processCreate charts, drawings and pictures for reports and presentationsPerformed other tasks as assigned.

Operate Line Machinery and support production linePerform instruction according Standard Operating Procedure documents per FDA , ISO standards and in compliance with Good Manufacturing Practices (GMP).

Participates in the review of design, manufacturing, inspection and test documentation to ensure that applicable program or contract quality requirements are met.Provides technical and advisory support to the prototype area to ensure the development of products in a manner that produces a quality system and documentation which will provide adherence to customer requirements.Performs program-specific tasks as required (e.g., customer-required First Article Inspection, Qualification Test Failure Analysis, etc.) to ensure compliance to individual program requirements and performing inspection PC Boards according to IPC-610.Establishes test requirements if not previously specified by the customer, and develops and directs the testing of existing and new-product prototypes to verify product reliability.Supports assigned operations group by activities such as providing visual aids and inspections analyses and performs failure analysis activities and tests under the supervision of more senior engineers.Work on all type of rework, testing and update according to Engineering Change Requests.Installation of fixtures, changes in workstations, changes to inspection analyses and changes to process procedures.Evaluates discrepant hardware in accordance with quality requirements, and determines its disposition or referral to the Material Review Board.Trains to acquire the skills and experience needed to perform the Quality Technician function independently. Adjust, repair, or replace electrical or electronic component parts to correct defects and to ensure conformance to specifications.Read and interpret schematic drawings, diagrams, blueprints, specifications, work orders, and reports in order to determine materials requirements and assembly instructions.Adjust, repair, or replace electrical or electronic component parts to correct defects and to ensure conformance to specifications.

Support activities to ensure compliance to the quality system regulations (e.g. 21CFR820, ISO13485). Oversee the inspection and testing activities for in-process and final product and /or conduct quality control inspections and review production records.Product Release/Authorization for Shipment. Collect data for quality system trending. Manage product and component quarantine, label control, and initial control of returned product. Analyze product complaints and prepare customer complaint investigation reports. Possess working knowledge of terms and concepts such as AQL, lot size, sample size, acceptance number, switching rules, sampling plans, zero-defect sampling, etc. Set and design test apparatus, fixtures, jigs, etc. Perform testing, records data, analyze and generates reports. Perform random audits of manufacturing work areas and/or documentation; in compliance with Good Manufacturing Practices (GMP). Provide technical assistance to engineering personnel and R&D (i.e. processes setting adjustments, problem solving, equipment verification and general training).Prepare and maintain the Design Change Order (DCO) files. Work in issuing, tracking maintaining CAPA System and DCR (NCMR's). Prepare and write validation protocols for product and processes (IQ, OQ and PQ). Work with R&D in the creation, review, approval, and maintenance of design documentation. Generate and update Standard Operating Procedure documents per FDA and ISO standards.

Read / interpret / understand basic and complex written procedures. (i.e., SOPs, OP Sheets, Drawings, Engineering Specs) Examine randomly selected samples of in process assembled and/or un-assembled parts for possible defects, utilizing unaided eye and/or aided eye methodology. Perform complex visual and/or mechanical Inspections functions with no direct supervision / monitoring / follow up. Perform complex mechanical testing of manufactured parts prior to shipment. Produce and update Standard Operating Procedure documents per FDA and ISO standards. Perform and write validation protocols for product and processes PPQ, IQ, OQ, PQ and MPQ, participate in Kaizen to implement lean line. Prepare and maintain the Design Change Order (DCO) files. Work in issuing, tracking and maintaining CAPA System. Conduct audits to production line to examine procedures practice. Interface with peers, Supervision, engineering, and management, professionally and respectfully. Assist the R&D in projects on creation, review, approval, and maintenance of design documentation. Proficient in Microsoft Office and ability to demonstrate basic computer skill set. (i.e., use of Excel, Microsoft Word. etc.) (Utilizing computer based equipment programs, etc.)Perform and demonstrate Math aptitude. (Algebra, geometry, addition, subtraction, division, multiplication, statistics, in all units of measure. etc.) Accurate and legible data recording/calculations in logbooks, etc., on work completed and/or performed. Ensure personal and peer adherence to all applicable FDA / GMP / ISO / State / Local /Company / Health-Safety / Environmental policies. Report infractions to supervision. Set up and use of equipment utilized by job function. (i.e., computer program file selections, microscope, micrometers, calipers, pin gauges, Instron, etc.) Ensuring conformance to specifications.

Calibration of working standards In-House, use standards procedure to calibrate and repair standard testing equipment.Prioritize maintenance activities ensuring all equipment within the facility are serviced to unacceptable standard in a timely and safe manner. * Conduct scheduled preventative maintenance activities. Troubleshoot equipment and perform corrective maintenance in breakdown situations. Installation of new equipment.Made sure that equipment is checked regularly for safety reasons.Coordinated and performed installations, maintenance, calibrations, and repairs.Interpreted maintenance manuals, schematics, and wiring diagrams.

Perform mechanical and electrical inspection of the product after manufacturing test and calibration has been completed with proper procedure. Summit the Quality Control Test Report, data package, if applicable, Certificate of Compliance/Conformance, customer purchase order to the Quality Assurance Manager for order release documentation and appropriate authorization. Troubleshoot and isolate problems on customer returns.Performed electronic repair to board and component level equipment. Interacted with engineers, technicians, and production personnel regarding testing procedures and results.Maintained and operated complex electronic test equipment and test stations.Demonstrated the quality assurance procedures to customers on factory visits.Performed Quality Audits at the factory.Investigated new equipment installed in the factory to make sure that it would comply with quality assurance procedures.

Conferred with performers, and others in order to determine and achieve the desired sound for a production such as a musical recording or a film. Set up, tested, and adjusted recording equipment for recording sessions and live performances; put down equipment after event completion. Regulated volume level and sound quality during recording sessions, using control consoles. Prepared for recording sessions by performing activities such as selecting and setting up microphones. Reported equipment problems, and ensured that required repairs are made. Mixed and edited voices, music, and taped sound effects for live performances and for prerecorded events, using sound mixing boards. Synchronized and equalized prerecorded dialogue, music, and sound effects with visual action of motion pictures or television productions, using control consoles. Recorded speech, music, and other sounds on recording media, using recording equipment. Reproduced and duplicated sound recordings from original recording media, using sound editing and duplication equipment. Separated instruments, vocals, and other sounds, then combine sounds later during the mixing or post-production stage. Set up, adjust, and operate audiovisual equipment such as cameras, film and slide projectors, and recording equipment, for meetings, events, classes, seminars and video conferences.