MES MOM Associate Manager

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

MES MOM Associate Manager (Accenture LLP; New York, NY)

Accenture LLP has multiple openings for the position of MES MOM Associate Manager in New York, NY, and the job duties are as follows:

• Participate 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.
• Document MES configuration and validation of EBRs.
• Collaborate with business management and users to strategically define needs and design solutions.
• Develop and sustain client relationships and respond to requests for 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.

BASIC QUALIFICATIONS

Must have a bachelor’s degree in Computer Science, Technology, Computer Information Systems, Computer Applications, Engineering, Business Administration, or related field, plus 5 years of progressive post-baccalaureate experience in the IT manufacturing industry.

Must have 4 years of experience in each of the following:

• Authoring and utilizing in Korber PAS-X solutions in an automated Life Sciences manufacturing environment;
• Working in a highly regulated manufacturing environment with Good Manufacturing Practice guidelines (CGMP); and
• Converting Life science industry business processes into electronic batch records.

Must have 3 years of experience in each of the following:

• Designing and executing Manufacturing Execution Systems (MES) testing scripts;
• Working with MES author teams in pharmaceuticals manufacturing;
• Utilizing Software Development Life Cycle and Validation in a Life Sciences manufacturing environment; and
• Conducting requirements gathering workshops using Korber PAS-X with life science clients.

Must have willingness and ability to travel domestically approximately 80% of the time to meet client needs.

Pursuant to the New York Transparency Bill, the offered wage for this role is $193,461.00 to $193,461.00 per year.

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