Lynne Thompson is a seasoned Technical Communicator at Thompson & Talian Communications, a company renowned for delivering high-quality communication solutions. With over a decade of experience in the field, Lynne specializes in translating complex technical concepts into easy-to-understand language for diverse audiences. She holds a bachelor's degree in English, and years working for technical companies, which has equipped her with a strong foundation in technical writing, editing, and research. Lynne is known for her exceptional ability to simplify and communicate intricate information, making her a vital asset to her company. She continues to embrace the latest trends in technology to further enhance her skills and deliver top-notch services that align with her client’s needs.More...
Montserrat Pou Prats
Quality Management Systems Consultant
Verified
Industrial Engineer graduated from the Santo Domingo Technological Institute (INTEC) with an Executive Master in Integrated Systems Management: Quality, Environment and Occupational Risk Prevention from the School of Industrial Organization (EOI) in Madrid, Spain. Certified Calibration Technician. Six Sigma Green Belt. Certified Lead Auditor in ISO 9001:2015. Internal auditor of quality management systems ISO 9001 and ISO 13485. Certification in Quality Management and Operational Excellence from the American Society of Quality (ASQ CMQ/OE). Certified Auditor of the American Society of Quality (ASQ CQA). Certification as a Supplier Quality Professional (ASQ CSQP).
Administration of Management Systems for the regulated medical device industry as a management representative. More than 15 years of experience in internal and third-party audits. Experience in audits of Quality and Environmental Management Systems. Experience in preparing and managing inspections by government institutions (FDA / MISPAS) and certification bodies in ISO standards, as well as compliance audits under the MDSAP (Medical Device Single Audit Program) structure.
Experience in Quality Operations Management in the FDA-regulated Medical Device manufacturing industry: manufacturing of sterile medical devices in controlled environments (GMP + BPD / GMP + GDP), implementation of sampling plans, in-process inspection, investigation of non-conformities and root cause determination, release of sterile product, development and implementation of product and process improvement plans and validations. Corrective and preventive actions (Internal and Suppliers), customer complaints, audits of manufacturing processes. Design and improvement of standardized products and processes.More...