QA Tester
1 week ago
Ask ITC Inc. which is backed by a $500 million Microtek group company, provides an industry leading blend of technology, business consulting, and outsourcing services.
Ask IT is a minority-owed enterprise; it has been founded on providing the highest quality possible and on the devotion to customer satisfaction.
Job DescriptionNC FAST requires the services of 16 Test Scripts Writers to support development and implementation of NC FAST Project 4 modules.
The NC Department of Health and Human Services seeks a contractor resource to assist with the development and implementation of NC Families Accessing Services through Technology (NC FAST) as a Test Scripts Writer. Duties include analyzing business requirements for testability and completeness using Functional Specification Documents, Business Requirements Documents and Technical Design Documents, developing requirements into test conditions, cases and scripts, development and execution of automated scripts using HP Quality Center to thoroughly test software to ensure proper operation and freedom from defects. This position is responsible for reviewing test cases and other testing artifacts to ensure the accuracy and completeness of all test artifacts. This position coordinates testing, reports and tracks testing problems by providing reproducible test cases, works with other product team members to diagnose and recreate problems as well as prioritize and implement solutions and close problem reports. This position is responsible for test scripting data collection and analysis according to the project plan schedule and ensuring adherence to standard practices and procedures.
Experience and proficiency in using HP test tools including Test Director/Quality Center 9.0 or higher and Quick Test Professional (QTP) 9.5 or higher
Experience testing web, GUI, client/server, and database applications.
Experience with requirements analysis and automated test cases/script development.
Experience with manual or automated testing, testing tools, writing test plans and reviewing test cases.
Strong analytical and problem solving skills.
Good oral and written communications skills in order to interact on a daily basis with system developers, business analysts, and others.
Ability to prioritize tasks within the project and work with minimal supervision or guidance.
Ability to work in a rapidly changing environment.
Stable work history
Experience with testing Curam products.
Experience testing for a health and human services project.
Experience with executing SQL to validate or test.
Experience navigating on a UNIX platform.
Experience developing and executing Selenium automation test scripts.
All your information will be kept confidential according to EEO guidelines.
-
Manufacturing Supervisor, Downstream
1 week ago
Durham, North Carolina, United States KBI Biopharma Full timeJob Summary:The Supervisor, Manufacturing, Downstream leads a team of downstream manufacturing associates to perform downstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The Supervisor will plan, assign, and monitor daily tasks to ensure timely "Right First Time" execution and strict compliance with safety...
-
Downstream Manufacturing Associate I/II
2 weeks ago
Durham, North Carolina, United States KBI Biopharma Full time $60,000 - $120,000 per yearThis position is on a 2-2-3 shiftDay Shift (6am-6pm)The Manufacturing Associate I/II(Manufacturing Associate)is responsible for performing upstream or downstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The Manufacturing Associate must follow written, approved procedures and forms to ensure all work is...
-
KBI: US
2 weeks ago
Durham, North Carolina, United States KBI Biopharma Full time $60,000 - $90,000 per yearThis position is on a 2-2-3 shiftNight Shift (6pm-6am)The Senior Manufacturing Associate I/II (Sr. Manufacturing Associate) is responsible for performing upstream or downstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The Sr. Manufacturing Associate must follow written, approved procedures and forms to...
-
Automation QA
1 day ago
Durham, NC, United States Insight Global Full timeIdentify, plan and execute testing activities to ensure high quality software and ensure compliance according to regulatory statues, policies and procedures. Test Web Application software, including Java and .Net. Test Web Services, Test applications which utilize IBM's MQ Series platform. Perform white-box tests. Create and maintain test plans, cases and...
-
Automation QA
7 days ago
Durham, NC, United States Insight Global Full timeIdentify, plan and execute testing activities to ensure high quality software and ensure compliance according to regulatory statues, policies and procedures. Test Web Application software, including Java and .Net. Test Web Services, Test applications which utilize IBM's MQ Series platform. Perform white-box tests. Create and maintain test plans, cases and...
-
Automation QA
3 days ago
Durham, NC, United States Insight Global Full timeIdentify, plan and execute testing activities to ensure high quality software and ensure compliance according to regulatory statues, policies and procedures. Test Web Application software, including Java and .Net. Test Web Services, Test applications which utilize IBM's MQ Series platform. Perform white-box tests. Create and maintain test plans, cases and...
-
Automation QA
5 days ago
Durham, NC, United States Insight Global Full timeIdentify, plan and execute testing activities to ensure high quality software and ensure compliance according to regulatory statues, policies and procedures. Test Web Application software, including Java and .Net. Test Web Services, Test applications which utilize IBM's MQ Series platform. Perform white-box tests. Create and maintain test plans, cases and...
-
Automation QA
1 day ago
Durham, NC, United States Insight Global Full timeIdentify, plan and execute testing activities to ensure high quality software and ensure compliance according to regulatory statues, policies and procedures. Test Web Application software, including Java and .Net. Test Web Services, Test applications which utilize IBM's MQ Series platform. Perform white-box tests. Create and maintain test plans, cases and...
-
Fill/Pack Operations Supervisor
4 weeks ago
Durham, United States Iviva Medical Full timeFill/Pack Operations Supervisor For The Dry Powder Inhaler (Dpi) ProgramWe are the first publicly-traded biotech or pharmaceutical company to take the form of a public benefit corporation. Our public benefit purpose is to provide a brighter future for patients through the development of novel pharmaceutical therapies; and technologies that expand the...
-
Supervisor, Manufacturing Support
7 days ago
Durham, United States KBI Biopharma Full timePosition SummaryThis position operates on a 2-2-3 schedule, with 7:00 pm-7:00 am shifts. The Manufacturing Supervisor leads a team of manufacturing associates to perform upstream or downstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The Supervisor will plan, assign, and monitor daily tasks to ensure timely...
-
Manufacturing Supervisor, Solution Prep
4 days ago
Durham, United States KBI Biopharma Full timeManufacturing Supervisor, Solution PrepThe Manufacturing Supervisor, Solution Prep leads a team of manufacturing associates to perform both upstream and downstream preparation of solutions and growth media used for processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The individual will plan, assign, and monitor daily...
-
Manufacturing Supervisor, Solution Prep
7 days ago
Durham, United States KBI Biopharma Full timeJob SummaryThe Manufacturing Supervisor, Solution Prep leads a team of manufacturing associates to perform both upstream and downstream preparation of solutions and growth media used for processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The individual will plan, assign, and monitor daily tasks to ensure timely...
-
Manufacturing Associate I/II
2 weeks ago
Durham, United States KBI Biopharma Full timeThis position is on a 2-2-3 shiftBlue Shift (7am-7pm)The Manufacturing Associate I/II (Manufacturing Associate) is responsible for performing upstream processing for biopharmaceutical products. The Manufacturing Associate must follow written, approved procedures and forms to ensure all work is conducted “Right First Time” (RFT) following Good...