Location: Bangalore
Employment Type: Full-time
Reports To: Head, Implementations
About Leucine :
Leucine Inc. is a leading provider of cutting-edge AI-powered MES (Manufacturing Execution Systems) solutions tailored to the pharmaceutical industry. We empower our clients with a composable MES platform to streamline operations, ensure compliance, and improve manufacturing efficiency. Our mission is to enable pharmaceutical manufacturers to achieve world-class quality through digital transformation.
Role Overview
- As an MES Implementation Consultant, you will play a pivotal role in deploying Leucine’s MES solutions for our clients. You will be the bridge between our product and the client’s manufacturing processes, ensuring a seamless implementation that aligns with the client’s requirements and industry regulations. Your expertise will guide clients through the journey from discovery to go-live, ensuring successful adoption of our solutions.
Key Responsibilities
- Project Management:
- Client Engagement:
- Solution Design:
- Integration & Configuration:
- Testing & Validation:
- Training & Support:
- Documentation:
- Continuous Improvement:
Lead end-to-end MES implementation projects, including planning, resource allocation, and execution.
Ensure timely delivery of milestones and manage project risks effectively.
Collaborate with client stakeholders to gather and document business requirements.
Act as the primary point of contact for the client during the implementation lifecycle.
Conduct workshops to align MES functionality with client processes.
Analyze manufacturing workflows to design and configure MES solutions tailored to client needs.
Collaborate with the product and development teams to define customizations or integrations if required.
Manage the integration of MES with other systems like SAP, LIMS, DMS, or WMS.
Configure the MES application, including workflows, master data, and user roles.
Develop test cases and oversee system validation activities to meet regulatory compliance requirements (e.g., FDA, GMP).
Conduct user acceptance testing (UAT) and address issues promptly.
Provide training to client teams on MES usage and best practices.
Offer post-implementation support to ensure smooth adoption of the solution.
Create and maintain comprehensive project documentation, including business process maps, system configurations, and user manuals.
Gather feedback post-implementation to identify areas for improvement.
Work with internal teams to refine Leucine’s implementation processes and methodologies.
Qualifications
- Education:
- Bachelor’s degree in Engineering, Computer Science, or related field. Background in Chemical, Mechanical, or Industrial Engineering is a plus.
- Experience:
- 3–5 years of experience in implementing MES or related enterprise systems in the pharmaceutical or manufacturing industry.
- Hands-on experience with SAP, LIMS, or other ERP/MES systems is highly desirable.
- Skills:
- Strong project management and stakeholder management skills.
- Proficiency in understanding manufacturing workflows and processes.
- Knowledge of regulatory compliance requirements like FDA, GMP, or GAMP5.
- Excellent problem-solving and analytical skills.
- Strong communication and presentation skills.
- Certifications: PMP, Six Sigma, or MES-specific certifications are a plus.
Why join us?
- Be part of a high-growth SaaS company revolutionizing the pharmaceutical industry.
- Work with a talented and passionate team driving innovation in manufacturing solutions.
- Opportunities for professional development and career advancement.
- Competitive compensation and benefits package.
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What We Do
Leucine is an AI-powered platform that helps pharmaceutical manufacturers in staying compliant and audit-ready while ensuring their medicines reach the patients faster.
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 30 companies in over 300 pharma manufacturing facilities across 10 countries, including the US, India, Brazil, Mexico, UAE, and others. Our customers trust us in helping them deliver safe medicine in the hands of the patients across the world.
For more information visit: https://www.leucine.io
