Seeking an opportunity to further my experience within the Information Technology and Life Sciences industries that utilizes my knowledge and skills in the areas of TrackWise configuration, validation, systems administration, and technical writing.
Augusta’s DevOps solutions adopt end to end approach that enforces communication, collaboration, integration and automation that removes bottlenecks in software development and ensuring agile delivery for software-driven innovation.
Augusta’s DevOps Framework fills the gaps that exists between software development, quality assurance, and IT operations thereby enabling you to quickly produce software products and services, while improving operational performance significantly
Augusta helps you optimize your development and delivery pipelines. Get enterprise cloud architecture expertise and DevOps strategy to bring your innovations to market faster.
IWMW 2003 b4 QA for web sites (5 - The QA Focus Perspective)IWMW
Slides (5 - The QA Focus Perspective) used in workshop session B4 on "Catching Mistakes: QA for your Web site" at the IWMW 2003 event held at the University of Kent on 11-13 June 2003.
See http://www.ukoln.ac.uk/web-focus/events/workshops/webmaster-2003/sessions/index.html#workshops-b
Augusta’s DevOps solutions adopt end to end approach that enforces communication, collaboration, integration and automation that removes bottlenecks in software development and ensuring agile delivery for software-driven innovation.
Augusta’s DevOps Framework fills the gaps that exists between software development, quality assurance, and IT operations thereby enabling you to quickly produce software products and services, while improving operational performance significantly
Augusta helps you optimize your development and delivery pipelines. Get enterprise cloud architecture expertise and DevOps strategy to bring your innovations to market faster.
IWMW 2003 b4 QA for web sites (5 - The QA Focus Perspective)IWMW
Slides (5 - The QA Focus Perspective) used in workshop session B4 on "Catching Mistakes: QA for your Web site" at the IWMW 2003 event held at the University of Kent on 11-13 June 2003.
See http://www.ukoln.ac.uk/web-focus/events/workshops/webmaster-2003/sessions/index.html#workshops-b
Migrating clinical studies from one database to another (such as Oracle Clinical to Oracle Clinical or Oracle Clinical to Oracle InForm or Medidata Rave), is a complex process that requires a thorough understanding of clinical data management, technology, and the regulations that govern clinical trials.
In this SlideShare on clinical study migrations we:
Discuss reasons to migrate a clinical study
Provide an overview of the clinical study migration process
Look at validation, technical, and business considerations for migrating a clinical study
Present real-world case studies
Toward an integration of Web accessibility into testing processesGrupo HULAT
Authors: Mary Luz Sánchez, Lourdes Moreno
DSAI 2013: 5th International Conference on Software Development and Technologies for Enhancing Accessibility and Fightin Info-exclusion (November 2013, Vigo, Spain).
Toward an integration of Web accessibility into testing processes
Managing Process Scale-up and Tech Transfer MilliporeSigma
Are you involved with planning tech transfer of your drug product? Join this webinar to learn more about the regulations and considerations you need to consider and learnings from a case study.
According to ICH Q10, “The goal of technology transfer activities is to transfer product and process knowledge between development and manufacturing, and within or between manufacturing sites to achieve product realization. This knowledge forms the basis for the manufacturing process, control strategy, process validation approach, and ongoing continual improvement.”
As a result, there is an expectation for transfers to be performed in an organized, methodical manner with appropriate documentation. It is also expected that they happen between one Process Development group to another or to a Pilot Lab, from Process Development lab to clinical or commercial manufacturing, or from Process Development to external clinical manufacturing. Lastly, they may also happen between two company facilities at commercial scale, or between a company and an external contract manufacturing at commercial scale.
This presentation will cover points to consider for successful tech transfers with a focus on cGMP training requirements, and include lesson learned from real cases.
Presented by Guillaume Plane on September 22, 2016
Are you involved with planning tech transfer of your drug product? Join this webinar to learn more about the regulations and considerations you need to consider and learnings from a case study.
According to ICH Q10, “The goal of technology transfer activities is to transfer product and process knowledge between development and manufacturing, and within or between manufacturing sites to achieve product realization. This knowledge forms the basis for the manufacturing process, control strategy, process validation approach, and ongoing continual improvement.”
As a result, there is an expectation for transfers to be performed in an organized, methodical manner with appropriate documentation. It is also expected that they happen between one Process Development group to another or to a Pilot Lab, from Process Development lab to clinical or commercial manufacturing, or from Process Development to external clinical manufacturing. Lastly, they may also happen between two company facilities at commercial scale, or between a company and an external contract manufacturing at commercial scale.
This presentation will cover points to consider for successful tech transfers with a focus on cGMP training requirements, and include lesson learned from real cases.
Presented by Guillaume Plane on September 22, 2016
Guarda il webinar su Youtube! http://youtu.be/_GlXZAuQrJc
A CHI E' RIVOLTO:
Quality Assurance Managers, Test Managers, Testers, Senior Developers, Project Managers and Compliance Managers
DESCRIZIONE:
La tecnologia avanza rapidamente, impattando quasi tutti gli aspetti delle pratiche di test: il test agile, il test basato sui requisiti, test as a service e il testing crowdsource.
In questo webinar verrà illustrato un processo in 5 step, in grado di migliorare i processi di test, riducendo i costi e i tempi dei progetti.
Questo webinar metterà in evidenza i limiti e le problematiche dello sviluppo software e le metodologie per un suo immediato miglioramento.
AGENDA:
- Creare e gestire facilmente e velocemente test cases, defects, enhancement requests e test specifications - con Polarion LiveDocs
- Definire ed eseguire test runs con the Polarion Testing Framework
- Risparmiare tempo e denaro riutilizzando tutti i testing artifacts
- Integrare nei propri processi i test cases importandoli da MS Office
- Integrare completamente la gestione dei requisiti ai test e al defect management
- Gestire con Polarion le attività con tutti gli stakeholder.
Overview of Validation in Pharma_Katalyst HLSKatalyst HLS
Introduction to Validation Concepts in Pharma, Bio-Pharma, Medical Device, Cosmetics, Food, Beverages industry.
Contact:
Katalyst Healthcare’s & Life Sciences
South Plainfield, NJ, USA 07080.
E-Mail: info@KatalystHLS.com
Advantage Clinical: Clinical Research Training Online - Course and Learning M...Fraser Gibson
This slideshow introduces you to Advantage Clinical, our current course offerings, course development as well as showcases our custom built Learning Management System.
visit www.advantage-clinical.com to learn more
Accelerate your Kubernetes clusters with Varnish CachingThijs Feryn
A presentation about the usage and availability of Varnish on Kubernetes. This talk explores the capabilities of Varnish caching and shows how to use the Varnish Helm chart to deploy it to Kubernetes.
This presentation was delivered at K8SUG Singapore. See https://feryn.eu/presentations/accelerate-your-kubernetes-clusters-with-varnish-caching-k8sug-singapore-28-2024 for more details.
Migrating clinical studies from one database to another (such as Oracle Clinical to Oracle Clinical or Oracle Clinical to Oracle InForm or Medidata Rave), is a complex process that requires a thorough understanding of clinical data management, technology, and the regulations that govern clinical trials.
In this SlideShare on clinical study migrations we:
Discuss reasons to migrate a clinical study
Provide an overview of the clinical study migration process
Look at validation, technical, and business considerations for migrating a clinical study
Present real-world case studies
Toward an integration of Web accessibility into testing processesGrupo HULAT
Authors: Mary Luz Sánchez, Lourdes Moreno
DSAI 2013: 5th International Conference on Software Development and Technologies for Enhancing Accessibility and Fightin Info-exclusion (November 2013, Vigo, Spain).
Toward an integration of Web accessibility into testing processes
Managing Process Scale-up and Tech Transfer MilliporeSigma
Are you involved with planning tech transfer of your drug product? Join this webinar to learn more about the regulations and considerations you need to consider and learnings from a case study.
According to ICH Q10, “The goal of technology transfer activities is to transfer product and process knowledge between development and manufacturing, and within or between manufacturing sites to achieve product realization. This knowledge forms the basis for the manufacturing process, control strategy, process validation approach, and ongoing continual improvement.”
As a result, there is an expectation for transfers to be performed in an organized, methodical manner with appropriate documentation. It is also expected that they happen between one Process Development group to another or to a Pilot Lab, from Process Development lab to clinical or commercial manufacturing, or from Process Development to external clinical manufacturing. Lastly, they may also happen between two company facilities at commercial scale, or between a company and an external contract manufacturing at commercial scale.
This presentation will cover points to consider for successful tech transfers with a focus on cGMP training requirements, and include lesson learned from real cases.
Presented by Guillaume Plane on September 22, 2016
Are you involved with planning tech transfer of your drug product? Join this webinar to learn more about the regulations and considerations you need to consider and learnings from a case study.
According to ICH Q10, “The goal of technology transfer activities is to transfer product and process knowledge between development and manufacturing, and within or between manufacturing sites to achieve product realization. This knowledge forms the basis for the manufacturing process, control strategy, process validation approach, and ongoing continual improvement.”
As a result, there is an expectation for transfers to be performed in an organized, methodical manner with appropriate documentation. It is also expected that they happen between one Process Development group to another or to a Pilot Lab, from Process Development lab to clinical or commercial manufacturing, or from Process Development to external clinical manufacturing. Lastly, they may also happen between two company facilities at commercial scale, or between a company and an external contract manufacturing at commercial scale.
This presentation will cover points to consider for successful tech transfers with a focus on cGMP training requirements, and include lesson learned from real cases.
Presented by Guillaume Plane on September 22, 2016
Guarda il webinar su Youtube! http://youtu.be/_GlXZAuQrJc
A CHI E' RIVOLTO:
Quality Assurance Managers, Test Managers, Testers, Senior Developers, Project Managers and Compliance Managers
DESCRIZIONE:
La tecnologia avanza rapidamente, impattando quasi tutti gli aspetti delle pratiche di test: il test agile, il test basato sui requisiti, test as a service e il testing crowdsource.
In questo webinar verrà illustrato un processo in 5 step, in grado di migliorare i processi di test, riducendo i costi e i tempi dei progetti.
Questo webinar metterà in evidenza i limiti e le problematiche dello sviluppo software e le metodologie per un suo immediato miglioramento.
AGENDA:
- Creare e gestire facilmente e velocemente test cases, defects, enhancement requests e test specifications - con Polarion LiveDocs
- Definire ed eseguire test runs con the Polarion Testing Framework
- Risparmiare tempo e denaro riutilizzando tutti i testing artifacts
- Integrare nei propri processi i test cases importandoli da MS Office
- Integrare completamente la gestione dei requisiti ai test e al defect management
- Gestire con Polarion le attività con tutti gli stakeholder.
Overview of Validation in Pharma_Katalyst HLSKatalyst HLS
Introduction to Validation Concepts in Pharma, Bio-Pharma, Medical Device, Cosmetics, Food, Beverages industry.
Contact:
Katalyst Healthcare’s & Life Sciences
South Plainfield, NJ, USA 07080.
E-Mail: info@KatalystHLS.com
Advantage Clinical: Clinical Research Training Online - Course and Learning M...Fraser Gibson
This slideshow introduces you to Advantage Clinical, our current course offerings, course development as well as showcases our custom built Learning Management System.
visit www.advantage-clinical.com to learn more
Accelerate your Kubernetes clusters with Varnish CachingThijs Feryn
A presentation about the usage and availability of Varnish on Kubernetes. This talk explores the capabilities of Varnish caching and shows how to use the Varnish Helm chart to deploy it to Kubernetes.
This presentation was delivered at K8SUG Singapore. See https://feryn.eu/presentations/accelerate-your-kubernetes-clusters-with-varnish-caching-k8sug-singapore-28-2024 for more details.
UiPath Test Automation using UiPath Test Suite series, part 4DianaGray10
Welcome to UiPath Test Automation using UiPath Test Suite series part 4. In this session, we will cover Test Manager overview along with SAP heatmap.
The UiPath Test Manager overview with SAP heatmap webinar offers a concise yet comprehensive exploration of the role of a Test Manager within SAP environments, coupled with the utilization of heatmaps for effective testing strategies.
Participants will gain insights into the responsibilities, challenges, and best practices associated with test management in SAP projects. Additionally, the webinar delves into the significance of heatmaps as a visual aid for identifying testing priorities, areas of risk, and resource allocation within SAP landscapes. Through this session, attendees can expect to enhance their understanding of test management principles while learning practical approaches to optimize testing processes in SAP environments using heatmap visualization techniques
What will you get from this session?
1. Insights into SAP testing best practices
2. Heatmap utilization for testing
3. Optimization of testing processes
4. Demo
Topics covered:
Execution from the test manager
Orchestrator execution result
Defect reporting
SAP heatmap example with demo
Speaker:
Deepak Rai, Automation Practice Lead, Boundaryless Group and UiPath MVP
Dev Dives: Train smarter, not harder – active learning and UiPath LLMs for do...UiPathCommunity
💥 Speed, accuracy, and scaling – discover the superpowers of GenAI in action with UiPath Document Understanding and Communications Mining™:
See how to accelerate model training and optimize model performance with active learning
Learn about the latest enhancements to out-of-the-box document processing – with little to no training required
Get an exclusive demo of the new family of UiPath LLMs – GenAI models specialized for processing different types of documents and messages
This is a hands-on session specifically designed for automation developers and AI enthusiasts seeking to enhance their knowledge in leveraging the latest intelligent document processing capabilities offered by UiPath.
Speakers:
👨🏫 Andras Palfi, Senior Product Manager, UiPath
👩🏫 Lenka Dulovicova, Product Program Manager, UiPath
Encryption in Microsoft 365 - ExpertsLive Netherlands 2024Albert Hoitingh
In this session I delve into the encryption technology used in Microsoft 365 and Microsoft Purview. Including the concepts of Customer Key and Double Key Encryption.
Transcript: Selling digital books in 2024: Insights from industry leaders - T...BookNet Canada
The publishing industry has been selling digital audiobooks and ebooks for over a decade and has found its groove. What’s changed? What has stayed the same? Where do we go from here? Join a group of leading sales peers from across the industry for a conversation about the lessons learned since the popularization of digital books, best practices, digital book supply chain management, and more.
Link to video recording: https://bnctechforum.ca/sessions/selling-digital-books-in-2024-insights-from-industry-leaders/
Presented by BookNet Canada on May 28, 2024, with support from the Department of Canadian Heritage.
PHP Frameworks: I want to break free (IPC Berlin 2024)Ralf Eggert
In this presentation, we examine the challenges and limitations of relying too heavily on PHP frameworks in web development. We discuss the history of PHP and its frameworks to understand how this dependence has evolved. The focus will be on providing concrete tips and strategies to reduce reliance on these frameworks, based on real-world examples and practical considerations. The goal is to equip developers with the skills and knowledge to create more flexible and future-proof web applications. We'll explore the importance of maintaining autonomy in a rapidly changing tech landscape and how to make informed decisions in PHP development.
This talk is aimed at encouraging a more independent approach to using PHP frameworks, moving towards a more flexible and future-proof approach to PHP development.
Observability Concepts EVERY Developer Should Know -- DeveloperWeek Europe.pdfPaige Cruz
Monitoring and observability aren’t traditionally found in software curriculums and many of us cobble this knowledge together from whatever vendor or ecosystem we were first introduced to and whatever is a part of your current company’s observability stack.
While the dev and ops silo continues to crumble….many organizations still relegate monitoring & observability as the purview of ops, infra and SRE teams. This is a mistake - achieving a highly observable system requires collaboration up and down the stack.
I, a former op, would like to extend an invitation to all application developers to join the observability party will share these foundational concepts to build on:
Elevating Tactical DDD Patterns Through Object CalisthenicsDorra BARTAGUIZ
After immersing yourself in the blue book and its red counterpart, attending DDD-focused conferences, and applying tactical patterns, you're left with a crucial question: How do I ensure my design is effective? Tactical patterns within Domain-Driven Design (DDD) serve as guiding principles for creating clear and manageable domain models. However, achieving success with these patterns requires additional guidance. Interestingly, we've observed that a set of constraints initially designed for training purposes remarkably aligns with effective pattern implementation, offering a more ‘mechanical’ approach. Let's explore together how Object Calisthenics can elevate the design of your tactical DDD patterns, offering concrete help for those venturing into DDD for the first time!
LF Energy Webinar: Electrical Grid Modelling and Simulation Through PowSyBl -...DanBrown980551
Do you want to learn how to model and simulate an electrical network from scratch in under an hour?
Then welcome to this PowSyBl workshop, hosted by Rte, the French Transmission System Operator (TSO)!
During the webinar, you will discover the PowSyBl ecosystem as well as handle and study an electrical network through an interactive Python notebook.
PowSyBl is an open source project hosted by LF Energy, which offers a comprehensive set of features for electrical grid modelling and simulation. Among other advanced features, PowSyBl provides:
- A fully editable and extendable library for grid component modelling;
- Visualization tools to display your network;
- Grid simulation tools, such as power flows, security analyses (with or without remedial actions) and sensitivity analyses;
The framework is mostly written in Java, with a Python binding so that Python developers can access PowSyBl functionalities as well.
What you will learn during the webinar:
- For beginners: discover PowSyBl's functionalities through a quick general presentation and the notebook, without needing any expert coding skills;
- For advanced developers: master the skills to efficiently apply PowSyBl functionalities to your real-world scenarios.
GenAISummit 2024 May 28 Sri Ambati Keynote: AGI Belongs to The Community in O...
CV - Cathleen Thompson
1.
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Cathleen Thompson
CathleenMThompson@gmail.com
Raleigh, NC (443) 827-2368
Objective
Seeking an opportunity to further my experience within the Information Technology and Life
Sciences industries that utilizes my knowledge and skills in the areas of TrackWise
configuration, validation, systems administration, and technical writing.
Skills
Hands-on Experience with TrackWise:
• Configuration, administration, installation, and upgrades
• Migration planning, management, and execution
• Use of integration/import utilities
• TrackWise Coordinator configuration and testing
• Crystal Reports development
Validation & Compliance Skills:
• User and functional requirements gathering, assessment, and documentation
• Development and execution of IQ, OQ, and PQ protocols
• Analysis and development of process workflows
Systems Administration:
• User access management
• Corrective and preventive maintenance
• User support for laboratory instrument applications
GxP Documentation Development
• Standard Operating Procedures (SOPs) Development
• Validation Documentation Creation
2. Cathleen Thompson
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Experience
Sequence | Morrisville, NC
Consultant I December 2015 – August 2016
Client: Major Pharmaceutical Product Development and Manufacturing Company
QC IT Administrator
• Laboratory Instrument Applications Administration:
o User Access Management
o Corrective and Preventive Maintenance
o Documentation Development
• GMP Laboratory Environment
• Cross departmental process development
Globiox | Austin, TX
Validation Specialist January 2013 – November 2015
Client: Major Semiconductor Equipment Manufacturing Company
TrackWise Administrator
• Led requirement workshops with system owners and SMEs
• Configured TrackWise workflows and projects with all associated customizations
• Investigated and resolved issues with existing TrackWise configuration, per functional
requirements
• Scheduled and executed migrations of TrackWise configurations from Development,
to QA, to Production environments
• Led Knowledge Transfer sessions for future Admins to comprehensively demonstrate
the implementation and routine administration of a configured TrackWise system
• Assisted with the development of User Acceptance Test scripts and training scripts for
the TrackWise system
Client: Major Pharmaceutical Product Development Company
Technical Writer
• Contributed to the development of a new System Life Cycle (SLC) process and
supporting infrastructure, in compliance with GxP standards
• Developed SOPs and templates to be used in authoring documents throughout the
SLC, including:
o Requirements documentation
o Testing documentation (including validation)
3. Cathleen Thompson
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o Support documentation (operations and maintenance)
o Reporting documentation
• Developed SLC policy documentation and Visio process diagrams
• Assisted with creation of SharePoint site for document and process management
Client: Contract Research Organization, Genomics Division
Validation Specialist
• Drafted the IOQ and PQ protocols for laboratory equipment in R&D and GMP facilities:
o Sage Sciences Blue Pippin DNA Size Selection System
o Roche 454 Genome Sequencer FLX+
o Covaris S220 Ultrasonicator
o Eppendorf epMotion 5070 Automated Liquid Handling System
o PerkinElmer LabChip XT Nucleic Acid Fractionation System
• Drafted URSs and SOPs for the equipment being validated, and revised as necessary
based on input from stakeholders and SMEs
• Assessed quality of past validation documentation
Internal to Globiox
Validation Specialist
• Executed OQ of custom Globiox software used for automated generation of TrackWise
validation documentation
• Performed multiple TrackWise installations and upgrades, versions ranging from 8.3 to
8.7
• Validated TrackWise workflows and custom configurations
• Played a supporting role in a number of consulting projects being managed by Globiox
• Assisted with other administrative tasks for the start-up, as needed
DrinkMore Custom Water | Gaithersburg, MD
Administrative Assistant July 2011 – May 2012
• Managed inventory during daily production of pallets of customized bottles of water,
balancing storage constraints for supplies
• Served as the liaison between the executive and warehouse personnel
• Trained all new personnel as the company grew
• Clientele quadrupled during the 10 months of employment
4. Cathleen Thompson
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Education
Sparta Systems | Hamilton, NJ
2014 - TrackWise Training Courses and associated Partner Accreditation Exams
• Introduction to TrackWise
• Technical Fundamentals of TrackWise
• Introduction to TrackWise Configuration and Administration
• Intermediate TrackWise Configuration and Administration
• Crystal Reports Design for TrackWise
Montgomery College | Rockville, MD
2013 - Associate of Arts, Computer Science