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Leucine

No-code platform automating compliant drug manufacturing

MES Engineer: Pharmaceutical & Biotech Manufacturing

Implementation & Technical Account ManagementConfirmed live in the last 24 hours
Full-timeBengaluru, Karnataka, India₹800k - ₹1.8M

About the Job

Requirements

  • At least 2 years of MES implementation or consulting experience in pharmaceutical, biotech, or life sciences.
  • Hands-on experience with at least one major MES platform, such as Leucine MES, Körber PAS-X, Emerson Syncade, Siemens Opcenter, FactoryTalk PharmaSuite, or GE Proficy.
  • A solid understanding of pharmaceutical manufacturing processes, electronic batch records, recipes, and production execution.
  • Practical experience with MES configuration, documentation, testing, and validation support.
  • Knowledge of system integration, including ERP–MES interfaces, L3–L2 integration, and APIs.
  • Ability to turn requirements into MES documentation, workflows, configurations, and test cases.
  • Working knowledge of GMP, GAMP 5, data integrity, EU Annex 11, and 21 CFR Part 11, applied in MES work.
  • Hands-on experience with batch processes in pharmaceutical or biotech manufacturing.
  • Proven experience with MES platforms, electronic batch records, testing, and validation.

Responsibilities

  • Work on MES projects from start to finish, including requirements gathering, design, configuration, testing, deployment, and hypercare.
  • Analyze manufacturing processes and translate them into MES functional and technical requirements, workflows, and configurations.
  • Configure MES solutions to fit client operations, including electronic batch records, recipes, production workflows, and master data.
  • Design and deliver integrations with enterprise systems such as ERP, LIMS, WMS, and QMS, and with shop-floor (L2) equipment and automation systems.
  • Find and fix system issues promptly to keep production downtime low.
  • Apply GMP, GAMP 5, data integrity (ALCOA+), EU Annex 11, and 21 CFR Part 11 to MES work.
  • Prepare validation deliverables and help execute them, including specifications, IQ/OQ/PQ test scripts, and traceability matrices; follow computerized system validation (CSV) and computer software assurance (CSA) principles.
  • Help with deviations, root-cause analysis, and corrective and preventive actions (CAPA).

Desired Qualifications

  • Experience with digital transformation or Industry 4.0 initiatives.
  • Experience with cloud-based or SaaS MES solutions.
  • Certification in an MES platform or related technology.
  • Working knowledge of SQL Server or Oracle databases.
  • Hands-on SAP integration experience, for example PP-PI, MM, and QM.

About the Company

Leucine

No-code platform automating compliant drug manufacturing

Leucine.io provides a no-code orchestration platform for drug manufacturing that helps QA, manufacturing, and QC teams convert paper procedures into digitally signed, self-executing work instructions. Its Process Builder digitizes workflows, captures data, and enforces verifiable steps with built-in cGMP-compliant protocols. The system logs all quality events and offers dynamic batch scheduling suggestions to improve efficiency and compliance, with a subscription model targeting Fortune 500 pharmaceutical companies. The platform differentiates itself by offering ready-made compliance workflows, centralized logging, and scalable customization in a no-code interface tailored for large manufacturers.

Company size
51-200
Company stage
Series A
Total funding
$8M
Headquarters
Bengaluru, India
Founded
2015

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