MES Implementation Consultant

Overview

Hybrid
$60 - $70
Full Time
No Travel Required

Skills

GxP
GMP
Health Care
Life Sciences
Manufacturing Execution System
Requirements Elicitation
Enterprise Resource Planning
Change Control
Biotechnology
Pharmaceutics
Manufacturing Engineering
MES

Job Details

Role- MES Implementation Consultant
Location: Princeton, NJ (Hybrid)
Duration:: 2-3 Years

Visa- NO OPT & H1B
Description

Our client is a global technology company, delivering industry-leading capabilities centered around digital, engineering, cloud and AI, powered by a broad portfolio of technology services and products. Our client works across all major verticals, providing industry solutions for Financial Services, Manufacturing, Life Sciences and Healthcare, Technology and Services, Telecom and Media, Retail and CPG, and Public Services.
About the job

This position will be an essential contributor to a multi-year Manufacturing Execution System (MES) Implementation. The position will take a leading role in the End-to-End process, managing requirements gathering, strategy/planning, implementation, integration, employee training and testing/validation. The position will have traditional Business Analyst responsibilities, in conjunction with providing MES subject matter expertise throughout the full implementation lifecycle.

Responsibilities

  • Provide full operational and analytical support MES systems, mitigating risks, identifying and remediating gaps, and proactive monitoring and testing.
  • Develop and integrate essential MES applications based on global benchmarks, manufacturing workflows and process requirements.
  • Translate business and manufacturing needs into system functionality and technical specifications.
  • Integrate MES with other enterprise systems such as ERP (e.g., SAP), LIMS, and automation systems (PLC/SCADA), as needed.
  • Actively participate and advise on critical business requirements gathering and analyses, contributing with Computer System Validation (CSV) activities; author and review required validation documents.
  • Maintain compliance with GxP guidelines and internal quality and change control standards.
  • Actively collaborate with cross-functional teams including QA, IT, Manufacturing, Engineering, and all other potential business entities.

Requirements:

  • 8-10+ years of experience with full, End-to-End MES implementation projects, ideally in pharmaceutical/biotechnology sectors or consumer packaged goods. platforms
  • Comprehensive technical understanding of MES architecture, requirements, data analysis, configuration, and data management.
  • Ideal candidates will have substantial experience in GMP/GxP environments, demonstrating active working knowledge of existing and anticipated compliance guidelines.
  • Working knowledge of system integration tools/processes (ERP, LIMS, PLCs/SCADA).
  • Entrepreneurial, agile-based work approach, with a career history of successful MES implementations

Thanks & Regards.

Aviral Sapra

Voto Conulting LLC

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About Voto Consulting LLC