Ovii Job Board

MES Consultant - Life Sciences

Leucine

Bengaluru, India • Onsite - Bengaluru, India • Full-Time • 3-10 years

Posted 2026-06-30 Customer Success & Delivery

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Job Description

Ovii's Interpretation of the Role

The MES Consultant will lead end‑to‑end implementation of manufacturing execution system solutions for pharma and life‑science clients, ensuring compliance and seamless integration with ERP and LIMS platforms. The role blends technical configuration, process analysis, and stakeholder collaboration to drive digital transformation in regulated manufacturing environments.

Role Snapshot

  • MES implementation specialist
  • Pharma & biotech manufacturing focus
  • Full‑lifecycle project delivery
  • Cross‑functional stakeholder collaboration
  • Regulatory compliance expertise
  • ERP & LIMS system integration

Must-Have Requirements

  • MES implementation
  • Manufacturing process knowledge
  • MES platform experience
  • System integration (ERP/MES APIs)
  • Regulatory compliance (GxP, 21 CFR Part 11)
  • Problem solving
  • Communication & stakeholder management
  • System integration

Nice-to-Have Signals

  • Digital transformation / Industry 4.0
  • Cloud‑based MES
  • MES platform certification
  • Digital transformation
  • MES certification
  • life sciences
  • biotech

Work Setup

  • Location: Bengaluru, India
  • Work mode: ONSITE
  • Employment type: Full-Time

Not Specified in JD

  • Visa sponsorship
  • Salary range
  • Remote eligibility
  • Education requirement
  • Certifications
  • Travel
  • Security clearance
  • Coding test
  • Portfolio

What You'll Likely Work On

  • Lead MES implementation projects from requirements gathering through deployment and support
  • Analyze client manufacturing processes and translate them into functional and technical MES specifications
  • Configure, customize, and test MES solutions to meet client‑specific needs
  • Integrate MES with ERP, LIMS, and other enterprise systems while ensuring data integrity
  • Maintain compliance with GxP, FDA, and 21 CFR Part 11 regulations
  • Deliver user training, create documentation, and provide post‑implementation support
  • Troubleshoot system issues to minimize downtime and drive continuous improvement

Good Fit If You Have

  • Experience with digital transformation or Industry 4.0 initiatives
  • Exposure to cloud‑based MES deployments
  • Professional certification on MES platforms
  • Background in pharma, biotech, or life‑science manufacturing

Skills

  • MES platforms
  • Manufacturing process knowledge
  • System integration (ERP/MES APIs)
  • GxP / 21 CFR Part 11 compliance
  • Problem solving & analytics
  • Stakeholder communication
  • Digital transformation (Industry 4.0) – preferred
  • Cloud‑based MES – preferred
  • MES platform certification – preferred