Covances Global Specimen Solutions (GSS) business provides specialty services in the holistic specimen tracking space. GSS improves translational science in the drug discovery process through industry best practices and a uniquely powerful pipeline data management analytics solution. GSS reduces the time, cost and risk of specimen based research, while building robust, healthy data pipelines that optimize research opportunities Job Summary
Looking for:
Experience with writing, editing and executing automated validation scripts manually and/or using automated tools
Experience performing both manual and automated validation
Experience with writing automated validation scripts for GUI for Web, Mobile App (Native & Web), Data Driven Validation, Back-end Validation (Interface, Database, Data Process applications/services)
Preferred but not required skills
Experience setting up and implementing a new automated validation strategy/structure
Experience using tools such as Test Complete, SOAP UI Pro, Target Process
Experience training and providing knowledge transfer between team members
Experience working in a GxP or Clinical Trials software validation industry
Function Specific
Demonstrate the ability to complete basic level validation activities for a project effectively.
Support in the planning and establishment of timelines to meet or exceed business expectations for validations.
Support in the review of product specification documentation to create appropriate testing methodologies.
Support in the review of validation documentation to support projects.
Work with other team members to create appropriate testing environments to support the testing methodologies.
Ability to use the basic working knowledge of SOPs, validation standards, and work procedures to support senior members in suggestion of potential improvements
Metrics
Support senior members in the management of metrics.
Assist with investigating or resolving issues of quality as directed.Staff and Financial Management
Understand implications of activities to project budgets.
Process Improvement
Support senior members for suggestions of process improvements where issues are seen.
Support Six Sigma process improvement teams.Training / SOPs
Active member of SOP review teams as assigned.
Education/Qualifications:
BCA, B.E, B.Tech, in Computer Science degree preferably in the sciences or related field or one (1) year in a validation or regulatory position dealing with SOPS and computer systems requirement specification.
Experience:
Less than 1 year validation experience or equivalent work experience in a regulated (FDA, EPA, etc.) environment preferred.
Strong attention to detail.
Problem Solving/Logic Skills.
Strong communication and interpersonal skills.
Strong MS/Office skills in particular with Excel and Word.
Understanding of Electronic Software Validation systems, such as JIRA or TargetProcess preferred.
Employement Category:
Employement Type: Full time Industry: Bio Technology & Life Sciences Functional Area: IT Role Category: Software Test Engineer Role/Responsibilies: Systems Associate (Testing) GSS