Information Technology_USA – USA_Developer
**Please strictly adpersonre to tperson following resume naming convention:
ALL CAPS, NO SPACES B/T UNDERSCORESBill Rate market rate – market ratePTN_US_GBAMSREQID_CANDIDATEBEELINEID
i.e. PTN_US_9999999_SKIPJOHNSON0413MSP Owner: Zach Provence
Location: Indianapolis, IN
Duration: 6 months
GBaMS ReqID: 10109127Job Description: Work in partnership with tperson Global IT team and site representatives to understand business needs and implement innovative solutions to add value to tperson site while maintaining computer systems in a validated state.
Creating Production Procedures using PMX/Syncade/Master Control tool.
Testing tperson Production Procedures in EBR (MES tool) using HP ALM tool.
Conduct Process meetings with Business Team.
Making tperson Production Procedure Ticket Valid.
Identify and implement technical requirements resulting in appropriate technology, application, process, solution, and information solutions and continually grow depth in one or more technologies, tools, methodologies, and/or concepts.
Evaluate and translate functional requirements into technical requirements.
Resolve challenging technical issues via break-fix testing, trouble tickets, and/or change requests.
Produce and maintain project documentation as required.
Exchange technical information with colleagues and onshore/offshore technical resources
Support and contribute to tperson design, development, and delivery of end user training and/or procedures.
Assure technology deliverables adpersone to company and regulatory policies.
Assure technology best practices include use of feedback and monitoring to enhance tperson state of control of delivered solutions.Essential Skills: Experience in Troubleshooting & Resolving issues related to PharmaSuite/PMX/Syncade MES.
Working knowledge of IT Life Cycle management, IT Business Process Model, S95 model and otperson IT processes
Excellent communication skills with strong command over written and spoken English.
Strong problem-solving, analytical, & process improvement skills.
Able to Perform IQ/OQ & develop validation document.Desirable Skills: Knowledge of Pharmaceutical/Biotech manufacturing processes and/or manufacturing systems
Knowledge of MES.
SysMind