Job Description

Job Title: PharmaSuite MES Author

Role Location: Indianapolis, IN or Charlotte, NC

Office Location: Indianapolis, IN or Charlotte, NC

Duration of Role: 1+yr

Job Description:

• Lead in the design, development, documentation, and implementation of Rockwell FactoryTalk PharmaSuite (FTPS) Manufacturing Execution Systems (MES).
• Design/Author/Develop/Configure Electronic Batch Records (EBR).
• Implement MES solutions and integrate with ERP and control equipment.
• Documentation of MES configuration and validation of EBRs.
• Work closely with business management and users to strategically define the needs and design solutions that add value.
• Document and analyze the information needs of the business and ensure appropriate solutions are delivered according to GxP standards.
• Respond to requests for client proposals.
• Manage and develop client relationships.

Basic Qualifications:

• 5 years of work experience
• Travel may be required for this role - the amount of travel will vary from 0 to 100 depending on business need and client requirements
• A minimum of 1 year of experience with Rockwell FTPS MES solutions in a highly automated Life Sciences manufacturing environment
• Knowledge of FDA and GMP guidelines
• Understanding of Life Sciences validation processes
• Working knowledge of software Development Life Cycle SDLC and support methodologies
• High School Diploma or GED

Preferred Qualifications:

• Bachelor's or Associate's

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