MES Developer with Pharmasuite

Overview

On Site
Depends on Experience
Accepts corp to corp applications
Contract - W2
Contract - Independent
Contract - 12 Month(s)
No Travel Required

Skills

MES
Pharmasuite
PMX
Syncade
Master Control tool
Manufacturing Execution System
EBR
HP ALM

Job Details

Job Role: MES Developer with Pharmasuite Location: Indianapolis, IN (Day 1 Onsite) Duration: 6+ Months

ROLE DESCRIPTION:

Experience Required: 6 8 Years
Work in partnership with the Global IT team and site representatives to understand business needs and implement innovative solutions to add value to the site while maintaining computer systems in a validated state.
Creating Production Procedures using PMX/Syncade/Master Control tool.
Testing the Production Procedures in EBR (MES tool) using the HP ALM tool.
Conduct Process meetings with the Business Team.
Making the 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 the design, development, and delivery of end-user training and/or procedures.
Assure technology deliverables adhere to company and regulatory policies.
Assure that technology best practices include the use of feedback and monitoring to enhance the state of control of delivered solutions.

SUPERVISION:

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 other IT processes
Excellent communication skills with a strong command of written and spoken English.
Strong problem-solving, analytical, & process improvement skills.
Able to perform IQ/OQ & develop validation document
Knowledge of Pharmaceutical/Biotech manufacturing processes and/or manufacturing systems

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