MES MOM Associate Manager

1000 Accenture LLP Company; New York (NY); Sur place; USD 174 000 - 213 000; Plein temps

Résumé du poste

Accenture LLP in New York, NY seeks a MES MOM Associate Manager to design, implement, and validate Electronic Batch Records within MES, integrating with ERP and control equipment. You will develop documentation, SOPs, and support go-live activities.

The role requires 5 years of IT manufacturing experience, strong knowledge of Korber PAS-X, CGMP, and ~80% domestic travel; bachelor's degree in a related field is required. Accenture offers a collaborative, global environment.

Qualifications

• Bachelor’s degree in a related field (CS/Engineering/IT) plus 5 years progressive IT manufacturing experience.
• 4 years in Korber PAS-X solutions in automated Life Sciences manufacturing.
• 3 years in MES testing, MES authoring with pharma clients, SDLC/Validation in Life Sciences.
• Willingness to travel domestically up to 80%.

Responsabilités

• Participate in the design, development, documentation, and implementation of Electronic Batch Records (EBR) in the MES.
• Implement MES solutions and integrate with ERP and control equipment.
• Document MES configuration and validation of EBRs; develop SOPs and validation protocols.
• Support go-live and hyper-care activities; build client relationships and respond to proposals.

Formation

Bachelor’s degree in Computer Science/Technology/Engineering or related field

Description du poste

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.

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

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);
  • 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;
  • 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.

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