StarFish Medical
Vriti Chawla is a skilled professional with extensive experience in quality assurance and laboratory operations. Currently serving as a Business Systems QA at StarFish Medical since June 2024, Vriti previously worked at Rubicon Organics™ as a Quality Assurance Specialist focusing on Change Management and as a Quality Assurance Technician. Vriti's background includes a role as a Laboratory and Quality Control Analyst at ARC Medical Devices Inc., where significant contributions to R&D and quality control processes were made, including advanced data summarization and compliance with industry regulations. Vriti has also held positions at Breathe Medical Manufacturing Ltd. and Arterra Wines Canada, demonstrating proficiency in quality control and analytical processes across various production environments. Vriti holds a Bachelor of Science degree in Medical Biochemistry and Molecular Biology from the University of British Columbia, obtained in 2019.
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StarFish Medical
StarFish Medical provides award-winning design, development, and flexible manufacturing outsourcing services —100% dedicated to the medical device and life science marketplace. StarFish partners with innovative companies to create and manufacture breakthrough products for a full range of medical specialty areas including: Cardiovascular, Digital Health, IVD, Ophthalmology, Optics, Ultrasound, POC Assay Diagnostic Technologies, and Microfluidics. StarFish expertise includes electronics, mechanical, human factors and software systems engineering. Our proprietary Pathfinder™ process for medical device product definition saves clients time and resources throughout the technology and product development phases to commercialization. Prototype and low volume complex electro-mechanical production are delivered in ISO 13485 certified facilities with cleanroom capabilities in Toronto and Victoria Regulatory and quality system (QMS) consultants at StarFish provide technical regulatory assistance for FDA and Health Canada submissions, including IEC 60601 and ISO13485. Innovative Design and Development Electronic / software / mechanical engineering Industrial design / human factors engineering PathfinderTM product definition process Technology optimization Verification / validation / testing ISO 13485 certified QMS Integrated Manufacturing Seamless ramp from clinical trials to full production Deep engineering involvement & oversight Electro-mechanical / software expertise Customized cart specialists Optical instrument build and test Dedicated program manager Flexible Manufacturing New product introductions Supply-chain management North America facilities Depot repair & field service Sustaining / value engineering Class 100,000 cleanroom