MES/MOM Lead – Life Sciences Manufacturing

Accenture PLC; New York (NY); On-site; USD 174,000 - 213,000; Full time

Job summary

Accenture LLP in New York, NY is hiring a MES MOM Associate Manager to design, develop, and implement Electronic Batch Records in MES systems and to integrate MES with ERP and control equipment.

The role requires a bachelor’s degree in a related field and significant experience in regulated Life Sciences manufacturing, with strong focus on PAS-X, CGMP, and lifecycle validation. Willingness to travel domestically up to 80% is expected.

Qualifications

• Bachelor’s degree in a related field and 5 years IT manufacturing experience.
• 4 years in Korber PAS-X within a regulated Life Sciences manufacturing environment.
• 3 years in MES testing, MES authoring, and life sciences validation.

Responsibilities

• Participate in design, development, documentation, and implementation of Electronic Batch Records (EBR) in MES.
• Implement MES solutions and integrate with ERP and control equipment.
• Document MES configuration and validation of EBRs.
• Collaborate with management and users to define needs and design solutions.
• Develop client relationships and respond to requests for proposals.
• Create, revise, and document SOPs, validation protocols, and other controlled documents.
• Support go-live and hyper-care activities.

Skills

Regulatory compliance

Client engagement

Documentation

SOP development

Validation testing

Education

Bachelor’s degree in a related field

Tools

Korber PAS-X

Job description

Accenture LLP in New York, NY is hiring a MES MOM Associate Manager to design, develop, and implement Electronic Batch Records in MES systems and to integrate MES with ERP and control equipment.

The role requires a bachelor’s degree in a related field and significant experience in regulated Life Sciences manufacturing, with strong focus on PAS-X, CGMP, and lifecycle validation. Willingness to travel domestically up to 80% is expected.