Unlimited Job Postings Subscription - $99/yr!

Job Details

Manufacturing Execution Systems (MES) Manager

  2026-02-10     Accenture     Houston,TX  
Description:

Are you ready to embark on a journey to transform digital engineering and manufacturing? Join us and help world-class clients tackle their biggest challenges, delivering products and services that their customers adore - swiftly, efficiently, and sustainably.

At Accenture, we fuse powerful digital capabilities with profound engineering and manufacturing expertise through Industry X. We harness data and digital tools to assist our clients in reimagining their products and the processes behind them. By integrating engineering and manufacturing operations at every stage—from design and sourcing to manufacturing and servicing—we empower them to achieve exceptional productivity, drive growth, and meet sustainability goals.

In this role, you will:

  • Lead the design, development, documentation, and deployment of Körber PAS-X Manufacturing Execution Systems (MES).

  • Design, author, develop, and configure Electronic Batch Records (EBR).

  • Implement MES solutions while integrating with ERP systems and control equipment.

  • Document MES configurations and validate EBRs.

  • Collaborate closely with business management and users to define strategic needs and design solutions that deliver value.

  • Analyze business information needs and ensure that suitable solutions are implemented following GxP standards.

  • Respond to requests for client proposals and manage client relationships.

This position may involve travel, which will vary based on business and client requirements.

Requirements:

  • At least 5 years of experience with Körber PAS-X MES solutions in a highly automated Life Sciences manufacturing environment.

  • Bachelor's Degree or equivalent (minimum 3 years of relevant work experience). Candidates with an Associate's Degree must have at least 6 years of equivalent work experience.

Preferred Qualifications:

  • Familiarity with FDA and GMP guidelines.

  • Excellent written and verbal communication skills.

  • Ability to work within a team-oriented, collaborative environment.

  • Proven ability to facilitate meetings and effectively follow up on action items.

  • Understanding of Life Sciences validation processes.

  • Knowledge of the Software Development Life Cycle (SDLC) and support methodologies.

Compensation will vary based on numerous factors, including office location, specific role, skill set, and experience level.

If you're looking to make an impact in a dynamic environment, we encourage you to apply and bring your expertise to our team.


Apply for this Job

Please use the APPLY HERE link below to view additional details and application instructions.

Apply Here

Back to Search