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Laura Meyer

Implementation Coordinator - Operations at StarFish Medical

Laura Meyer is an experienced professional in operations and supply chain management with a focus on the medical device and aerospace sectors. Currently serving as Implementation Coordinator at StarFish Medical since August 2018, Laura manages system enhancements and oversees the onboarding of new applications. Prior to this role, Laura was Supply Chain Manager at Starfish Product Engineering, responsible for procurement and production control supporting new product development. Additional experience includes roles as Continuous Improvement Manager and Project Manager at Viking Air, where Laura managed multi-site programs and optimized business processes. Laura began a career at JDSU, contributing as Lean Facilitator and Lean Project Manager across multiple countries.

Location

Victoria, Canada

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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


Headquarters

Victoria, Canada

Employees

51-200

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