MES Program Lead for Life Sciences Manufacturing

Accenture PLC; United States; Hybrid; USD 94,000 - 294,000; Full time

Job summary

Accenture PLC in the United States seeks an ambitious Manufacturing Systems (MES) Manager to lead MES design, development, documentation and validation in a highly automated Life Sciences setting. You will collaborate with ERP and control systems, ensure GxP compliance, and define value-driven MES solutions for clients.

Travel may be required (0–100%), and you will work with client teams to drive SDLC processes and life sciences validation.

Qualifications

• Minimum 5 years of MES experience in Life Sciences manufacturing.
• Knowledge of FDA and GMP guidelines.
• Strong written and verbal communication skills.
• Understanding of SDLC and validation processes.
• Bachelor's degree or equivalent (minimum 12 years) work experience.

Responsibilities

• Lead design, development, documentation, and implementation of 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.
• Collaborate with management and users to define needs and design value-added solutions.
• Document and analyze information needs of the business and ensure MES meets GxP standards.
• Respond to requests for client proposals.
• Manage and develop client relationships.

Skills

MES expertise

SDLC knowledge

Life Sciences validation

Education

Bachelor's degree or equivalent

Job description

Accenture PLC in the United States seeks an ambitious Manufacturing Systems (MES) Manager to lead MES design, development, documentation and validation in a highly automated Life Sciences setting. You will collaborate with ERP and control systems, ensure GxP compliance, and define value-driven MES solutions for clients.

Travel may be required (0–100%), and you will work with client teams to drive SDLC processes and life sciences validation.