PharmaSuite MES Author

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