Interview Presentation
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Ricky Ghilarducci is a 29-year-old mechanical engineer seeking a new position. He has 5 years of experience in quality assurance and medical device engineering. He graduated from San Jose State University in 2005 with a BS in mechanical engineering and a minor in mathematics. His work experience includes positions at Abbott Diabetes Care, Calibra Medical, and MAP Pharmaceuticals, where he contributed to product development, manufacturing, and quality processes. He is enthusiastic and brings strong engineering skills, documentation experience, and communication abilities to a potential new role.
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C v a.madrigal ingles
This document provides a summary of an individual's experience working as a control process engineer and quality engineer. Over 10 years of experience is highlighted, including achievements in standardizing operations, reducing variability and costs, and increasing production volumes. Education includes a bachelor's degree in industrial engineering and various internal and external training courses in lean manufacturing, six sigma, medical device regulations, and ISO standards. Proficiency in process design, control, improvement, and quality management is demonstrated across roles in plastics manufacturing, medical devices, automotive, and electronics industries.
Robin C Pagaduan_QA
Robin Pagaduan is an experienced QA tester and systems analyst with over 15 years of experience in testing various software applications and websites. They have extensive experience testing healthcare applications such as those for Blue Cross Blue Shield of Rhode Island including testing websites, salesforce, security applications, and data integration. They also have experience testing CVS.com, managing other testers, and ensuring projects meet deadlines and quality standards. Robin Pagaduan has a track record of successfully implementing test strategies and resolving issues to deliver projects on time.
Leveraging Data to Develop, Execute and Exceed the Expectations of Your Regu...
Scientific data, homegrown or from published literature, is essential to your regulatory strategy…be it establishing substantial equivalence in FDA 510(k) applications, qualifying a device as a legitimate predecessor in the context of a Technical File for CE Mark, predicting the performance of a device in development, judging a new device in verification and validation testing and, with proper planning, expanding indications for use and identifying new marketable claims of performance (or mitigation of risk and liability). In this session, participants will be exposed to various vital data sources and obtain practical examples for putting them to meaningful use.
Andrew Ritchie Resume
Andrew Ritchie has over 15 years of experience in engineering roles in the pharmaceutical, consumer care, and medical device industries. He has expertise in project management, capital projects, equipment validation, and computer system validation. Currently he is an Engineering Director at Bayer Consumer Care where he manages engineers, consultants, and contractors supporting R&D equipment and facilities. Previously he held engineering leadership roles at Merck Consumer Care and Boston Scientific.
Stephen Keokhanthachone Resume Jan. 2017
The document is a resume for Stephen S. Keokhanthachone seeking a position utilizing his background in documentation specialization, quality assurance, and process engineering. It summarizes his experience developing and maintaining documentation systems for medical device production in compliance with quality standards. His resume lists responsibilities such as managing document control, ensuring proper documentation practices, training personnel, and assisting with audits from his roles at various medical technology companies.
Bob Price - Mechanical Engineer
Bob Price is a mechanical engineer with over 20 years of experience in product and process development for the medical device industry. He has experience designing components and fixtures, transferring products to manufacturing, and ensuring products meet necessary standards through testing. His skills include product development, process development, validation testing, CAD and machine shop skills. He is seeking a role where he can utilize his engineering and manufacturing experience.
Eva Harding Resume_2015
Eva Harding has over 20 years of experience in the medical device industry, primarily focused on quality engineering roles at Abbott Vascular. She has supported new product development programs from design controls through regulatory submissions. Her experience includes risk assessment, design validation, human factors engineering, and submissions for CE marking and US approval. She is looking to expand her career into a leadership role where she can help meet and exceed corporate goals.
Additive Manufacturing - Design Considerations Rapid Fire - OMTEC 2018
Easing the Secondary Production Process During Design: The design stage is where the smart decisions are made in additive manufacturing — not only on ways to increase clinical outcomes and additive processes, but also to ease post-processing. In these areas, the process can be made efficient and cost-effective. Receive tips and tricks on orientation, supports, stock material and design features.
Enhancing Design through Engineering and Manufacturing Collaboration: Unlike conventional methods, additive manufacturing requires design and manufacturing teams to work closely together very early in the design phase. In a world where the pace of innovation is nearly vertical, it’s imperative to understand this concept early to make additive manufacturing work for you. This discussion lends a high-level overview of best practices when working with internal or external suppliers, and shows examples of the use of additive manufacturing to create innovative medical device designs.
Rkramer Resume
Richard Kramer has over 30 years of experience leading engineering teams in product development, quality systems, and strategic planning across various industries. He is currently the Director of Engineering at a consulting firm, where he manages projects supporting R&D organizations. Previously he held management roles overseeing quality assurance, product development, and instrumentation development at medical device and pharmaceutical companies.
IVYWorks
The aim is to be a one stop service provider for consulting and support services related to compliance, validation, Computerized System Validation, IT Infrastructure Qualification and IT Solutions catering to clients in the life sciences industry. The main objective is to provide services that enhance current operations and bring the knowledge and experience needed to maintain, manage and control related services.
The philosophy of IVY Works is to be transparent, open and work with our Clients as part of their teams to achieve set objectives and goals.
Experience: Extensive experience among the founders in regulatory compliance, validation, CSV and IT Solutions. All consultants have relevant experiences in the life sciences industries with exposure to the whole gamut of operations (manufacturing, labs, IT, regulatory).
Exposure: Founders and Consultants have worked with a majority of the top ten Pharmaceutical companies in lead roles to manage and also better develop, implement and validate compliance processes. Have worked with clients in North America, Europe & Asia.
Performance: Proven track record of delivering ahead of budget and timelines for a variety of projects/ programs
Delivery: Ability to take on projects of any size – with the same emphasis on project delivery and management
08-24-2016 Terence Sauer
Terence Sauer has over 30 years of experience leading product development teams in engineering and technology companies. He currently works as Vice President of Engineering and Chief Technical Officer at Presco, Inc., where he manages project teams and helps the company achieve ISO certifications. Prior to this, he spent over 10 years as Director of Electrical and Systems Engineering at Smiths Detection, leading a team that developed chemical and radiation detection technologies.
Resume of Russell Stevens 2013
Russell Stevens has over 15 years of experience in semiconductor manufacturing, including roles managing new product development and business development. He has generated over $75 million in annual revenues across roles at ATMI and SACHEM. Stevens holds certifications in design for six sigma, project management, and product management.
Isker marlene frank 10 july2016-resume
Isker Marlene Frank has over 20 years of experience in project coordination, business analysis, documentation, and scientific analysis. She has extensive experience in regulatory compliance documentation, MS Office, various operating systems, and analytical techniques. Her background includes roles as a senior technical writer, technical writer III, legal documentation specialist, project coordinator, and engineering documentation specialist.
Vernon W Miller III Resume 12102015
Vernon W Miller III has over 15 years of experience in information technology, software development, cyber security, and project management. He has a Bachelor's degree in Information Systems and an Associate's degree in Information Technology. Miller currently works as a Cyber Security Specialist and Project Manager for SAIC, providing system engineering support and cybersecurity for the Marine Corps' medical systems. Previously he worked as a Database Administrator, Systems Analyst, and SME for the Army Test and Evaluation Command, and has also held roles at K&T Technologies, Wachovia Bank, and Master-Print.
Kerry Eubanks 2013-08-28
Kerry Eubanks has over 30 years of experience in reliability engineering. He has held roles at several companies developing and implementing reliability programs for lighting, agricultural, and industrial control systems. Currently, he is a Staff Reliability Engineer at Musco Sports Lighting where he develops reliability programs for lighting systems and provides manufacturing and field support. He has expertise in reliability risk assessment, failure analysis, and data analysis.
Resume 2016
Kimberly Caller is a business analyst with experience in project management, business process improvement, and software development. She has a master's certificate in management information systems and has designed inventory tracking, mobile healthcare, and chemical distribution systems. Her skills include requirements analysis, process modeling, and ensuring compliance with industry standards like GLP, cGMP, and ISO. She currently works as a business systems analyst at CommunityAmerica, where she facilitates agile development and improves business operations.
Similar to Interview Presentation (20)
Leveraging Data to Develop, Execute and Exceed the Expectations of Your Regu...
Leveraging Data to Develop, Execute and Exceed the Expectations of Your Regu...
Additive Manufacturing - Design Considerations Rapid Fire - OMTEC 2018
Additive Manufacturing - Design Considerations Rapid Fire - OMTEC 2018
Interview Presentation
- 1. Background & Achievements By: Ricky Ghilarducci January 25 th , 2010
Editor's Notes
- These issues include reduction in supply of fossil fuel resources, poor air quality and pollution due to automotive emissions, rising costs of automobile ownership, and growing urban congestion due to increasing numbers of automobiles on road and highway infrastructure. The project name for this vehicle is the Grand Tilting Racer or GTR. To address the above issues, our design approach is to move toward a smaller, narrower vehicle while maintaining most of the benefits associated with a standard car, such as comfort and handling. In order to make the vehicle smaller, we make a logical compromise by limiting the maximum capacity of the vehicle to no more than two occupants, or one occupant and some additional space for cargo. This design decision is justified on the basis that a high percentage of automobiles are used by only one occupant for most daily activities.