12 of the top 15 pharma generic companies in the world trust Leucine to manufacture the drugs that reach millions of patients every day.
Pharma manufacturing is one of the last large industries still running on paper, Excel, and tribal knowledge. A single missed step in a batch record can mean a recall, a regulatory warning, or a drug that should never have left the plant.
Leucine is the AI platform replacing all of it. Series A, backed by top-tier global investors, 60+ pharma enterprises in production, and the team that's going to define this category.
About the Role:
We are looking for a skilled and driven MES (Manufacturing Execution Systems) Consultant to join our growing team. In this role, you will be responsible for implementing, configuring, and optimizing MES solutions to enhance manufacturing efficiency, compliance, and digital transformation initiatives across our client base.
Key Responsibilities:
● Lead and support MES implementation projects across the full lifecycle (requirement gathering, design, configuration, testing, deployment, and support)
● Collaborate with cross-functional teams including manufacturing, quality, IT, and engineering stakeholders
● Analyse business processes and translate them into MES functional and technical requirements
● Configure and customize MES solutions based on client needs
● Ensure compliance with industry standards (GxP, FDA, etc.) where applicable
● Perform system integration with ERP, LIMS, and other enterprise systems
● Conduct user training, documentation, and provide post-implementation support
● Troubleshoot and resolve system issues, ensuring minimal downtime
● Drive continuous improvement initiatives and system optimization.
Requirements
● 3–10 years of experience in MES implementation/consulting
● Strong understanding of manufacturing processes, preferably in pharma, biotech, or life sciences
● Experience with MES platforms
● Knowledge of system integration (ERP/MES interfaces, APIs, etc.)
● Familiarity with regulatory requirements such as GxP, 21 CFR Part 11
● Strong problem-solving and analytical skills
● Excellent communication and stakeholder management abilities.
Preferred Qualifications:
● Experience in digital transformation or Industry 4.0 initiatives
● Exposure to cloud-based MES solutions
● Certification in MES platforms or related technologies
Benefits
Leucine is an AI-powered platform that helps pharmaceutical manufacturers stay compliant and audit-ready while ensuring the right first-time batch release.
Using Leucine, Manufacturing, QA, and QC teams can significantly increase productivity and reduce deviations from cGMP guidelines across thousands of complex regulated workflows from material receipt to batch release. Leucine supports manufacturers across all modalities such as small molecules, biologics, gene therapies, vaccines etc.
We have built industry's first AI framework, Leucine10x, which is designed to serve as a co-pilot in pharmaceutical manufacturing processes. Built on proprietary LLM technology, Leucine 10X offers an army of AI co-pilots that perform highly specialized tasks such as digitizing paper-based SOPs, creating a digital twin of the shop floor, collaborating with Production Managers in creating dynamic production plans, thus ensuring on-time batch delivery. Most significant is its ability to speed up Root Cause Analysis (RCA) of deviations in the manufacturing process by quickly analyzing data, including text-based records, logs, and even staff interview transcripts, to identify potential issues or patterns that might not be readily apparent.
Leucine is currently deployed at over 50 companies in over 300 pharmaceutical manufacturing facilities across 10 countries, including the US, India, Brazil, Mexico, UAE, and others. Our customers trust us to help them deliver safe medicine to patients worldwide.
For more information, visit: https://www.leucine.io
