Leucine - AI for Pharma

Leucine is transforming pharmaceutical manufacturing with its AI-powered platform that integrates manufacturing, quality, and laboratory operations. The company offers a suite of products designed to…

AIAutomationComplianceDigital TransformationLaboratoryManufacturingPharmaceuticalQuality Managementleucine.io

Leucine - AI for Pharma

AIAutomationComplianceDigital TransformationLaboratoryManufacturingPharmaceuticalQuality Managementleucine.io

HQNew York City, US

Team Size114

Open Jobs5

Total Funding$8M

Latest Fundraise3 years ago

TL;DR

What: AI-first software platform for pharmaceutical manufacturing, quality, and laboratory operations

Founded: 2019

Scale: Used by over 300 pharma facilities (company claim)

Recent funding: $7.0M Series A (Oct 16, 2023) led by Ecolab

Company Overview

Problem Domain

Pharmaceutical manufacturing operations, quality, and laboratory digitization and compliance

Founded

2019

Industry

Biotechnology

Tech Stack

Amazon CloudFront

Amazon S3

Amazon SSL

Cloudflare Network Error Logging

DNSSEC

Envoy

Google Universal Analytics

Hubspot Hosted

IPv6

Funding Track Record

Seed- 2020-06

$1,000,000

Recorded as ~ $1.0M seed

Series A- 2023-10-16

$7,000,000

Participants included Pravega Ventures, Axilor Ventures, Techstars and angel investors

Investor Signal

“Strategic investor participation (Ecolab) in Series A and participation from specialized VC and accelerator investors”

Founders

What we do

Join the Team

Solutions Architect

On-SiteBengaluru, Karnataka, IN

On-Site • Bengaluru, Karnataka, IN

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Key Responsibilities

Lead end-to-end solution design for pharmaceutical and life-sciences clients.
Translate complex business requirements into scalable, maintainable architectures.
Collaborate with product, engineering, QA and client teams to ensure on-time delivery.
Provide technical thought leadership and mentorship to junior architects and developers.
Drive proof-of-concepts, feasibility studies, and performance tuning initiatives.
Ensure compliance with industry regulations (e.g., 21 CFR Part 11, GMP).

Required Qualifications

2–5 years of consulting or industry experience in pharma, life sciences, or related sectors.
Bachelor’s in Chemical, Mechanical or Biotechnology Engineering (or closely related).
Demonstrated track record of architecting enterprise-grade software solutions.
Strong understanding of manufacturing workflows, validation processes and regulatory needs.
Excellent communication skills—able to present complex designs to non-technical stakeholders.
Preferred Experience & Sourcing Targets
Industry pedigree: candidates currently or formerly at Cipla, Dr. Reddy’s, Pfizer, Novartis, etc.
Consulting backgrounds: life-sciences practice at PwC, KPMG, McKinsey, BCG or similar.
Experience working with digital validation platforms, LIMS integrations or process-management tools.

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