MES MOM Associate Manager

Must have a bachelor’s degree in Computer Science, Technology, Computer Information Systems, Computer Applications, Engineering, or related field, plus 5 years of progressive post-baccalaureate experience in the Manufacturing industry.
Must have 3 years of experience in each of the following: Authoring and utilizing Körber PAS-X MES solutions in an automated life sciences manufacturing environment; Working in a highly regulated manufacturing environment with Good Manufacturing Practice guidelines (CGMP); and Life science industry business processes.
Must have 2 years of experience in each of the following: Leading and managing MES author teams in pharmaceuticals manufacturing; Designing and executing Manufacturing Execution Systems (MES) testing scripts; Utilizing Software Development Life Cycle and Validation in a life sciences manufacturing environment; and Leading requirements gathering workshops using Körber PAS-X with life science clients.
Must have willingness and ability to travel domestically approximately 25% of the time to meet client needs.

Lead in the design, development, documentation, and implementation of Electronic Batch Records (EBR) in the Manufacturing Execution Systems (MES).
Implement MES solutions and integrate with Enterprise Resource Planner (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.
Manage and develop client relationships and respond to requests for client proposals.
Create, revise, and document specification documents, validation protocols, Standard Operating Procedures (SOPs), executable forms, and other version-controlled documents.
Support go-live and hyper-care activities.

No preferred qualifications provided.