About us…
Online Business Applications, Inc. is a software product company located in Lemont, Illinois specializing in medical communications software for the pharmaceutical and biotech industries. Our product, IRMS (Information Request Managements Software) is used by over 60 of the worlds leading pharmaceutical and biotech companies and is currently in use in the United States, Canada, Europe, Asia and Australia. Our product uses the full capabilities of MS Access and Visual Basic (VBA) with interfaces to MS Word, MS Outlook, MS Excel, Lotus Notes, Adobe PDF and other PDF generators, FAX servers, SQL Server, Oracle, and other applications. Many of our clients are using our software via Citrix or Terminal Services for their global solution. However, we are currently converting our product to Microsoft’s .NET platform and a Web based environment. See our web site for more information about the company, our products, and our industry at www.irmsonline.com.
About the opportunity...
We are experiencing substantial and sustained growth and are in need of a training specialist to assist with client onsite training, training classes at our education center, web-based training, as well as assist to develop and maintain training programs and materials. Initially, you may be required to assist with client support. You will be required to frequently travel to client sites, mainly in the US.
We offer a casual work environment with paid vacation, personal days, sick days and holidays. A 100% fully-paid health insurance plan through Blue Cross Blue Shield of Illinois is provided for employee and family, as well as a salary based on your skills and experience. Please send your salary history and requirements along with your resume to lindsay.oles@irmsonline.com
ASP.NET VB.NET Web Application Developer
Responsibilities:
As part of the development team, you will be developing new code, modifying existing code, and performing unit testing. You will be required to provide second-tier client support for and with our technical support team.
We are currently converting our product to Microsoft’s .NET platform and a Web based environment. We are seeking a individual with a high level of experience developing applications using Visual Studio, ASP.NET, and VB.NET. We seek an individual who can step right in and become an integral part of our development team and possibly lead the development of our new applications.
Our legacy product uses the full capabilities of MS Access and Visual Basic (VBA) with interfaces to MS Word, MS Outlook, MS Excel, Lotus Notes, Adobe PDF and other PDF generators, FAX servers, SQL Server, Oracle, and other applications. Many of our clients are using our software via Citrix or Terminal Services for their global solution.
We utilize change control procedures and source code control via Source Safe. Your job will require communications with the project team, our clients, our support staff and our training staff. Excellent written and verbal communications skills are essential.
Minimum Qualifications for Consideration...
- 3 - 5 Years experience developing with Visual Studio, VB.NET, and ASP.NET
- 4-6+ years web development experience
- Full life-cycle development experience,
- SQL Server 2005 and Reporting Services
- Windows Forms 2.0
- VSTO, Data binding, UI Development, n-tier Development
- Web Service development (enterprise)
- Console apps and un-assisted execution development
Other Valuable Experience
- Microsoft Access with VBA or Visual Basic
- Oracle or SQL Server
- Microsoft Word and Microsoft Excel interfaces
- Install Shield or Windows Installer
- Citrix or Terminal Services
- Siebel Life Sciences
FDA Regulated Software Validation and Quality Assurance Analyst
Responsibilities:
As part of the Validation team, you will be leading or supporting validation efforts and deliverables for projects requiring validation. You will be responsible for creating Validation Plans, IQ’s, OQ’s, PQ’s, Validation Summaries, etc. Travel to our clients sites to lead the validation process is required and may total about 25%.You will be responsible for reviewing and evaluating validation assessments for our application. You will also be involved in reviewing and revising SOP’s as needed.
Your job will require communications with the project team, our clients, our support staff and our training staff. Excellent written and verbal communications skills are essential.
- Requirements Gathering onsite or offsite
- Customize User Requirements, Functional Specification, and Requirements Traceability Matrix to meet the clients needs
- Customize test scripts to challenge the requirements
- Develop Validation Templates
- Assist client during Validation protocol execution
- Prepare Validation Summary report
- Responsible for the entire validation process
- Co-ordinates all the validation activities
- Develop and revise company SOP as and when needed
- Review applications for 21 CFR Part 11 compliance
Requirements:
- 2+ Years experience with validated systems within a regulated industry
- Software Validation Experience and System Life Cycle methodology knowledge
- 21 CFR Part 11 Knowledge
- Experience writing Validation documents and Standard Operating Procedures
- Strong Organization skills
- Excellent Verbal and Written communication skills
- IT Background
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