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Leucine

No-code platform automating compliant drug manufacturing

Solution Delivery Architect

Implementation & Technical Account ManagementConfirmed live in the last 24 hours
Full-timeBengaluru, Karnataka, IndiaNo salary listedIn-person

About the Job

Requirements

  • Two to five years of consulting or industry experience in pharma, life sciences, or related sectors.
  • A bachelor's degree in Chemical, Mechanical, or Biotechnology Engineering, or a closely related field.
  • A demonstrated track record of architecting enterprise-grade software solutions.
  • A strong understanding of manufacturing workflows, validation processes, and regulatory needs.
  • The ability to present complex designs to non-technical stakeholders.

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, quality assurance, 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, including 21 CFR Part 11 and Good Manufacturing Practice.

Desired Qualifications

  • Experience or a current/former position at pharmaceutical companies such as Cipla, Dr. Reddy’s, Pfizer, or Novartis.
  • A consulting background in a life-sciences practice at PwC, KPMG, McKinsey, BCG, or a similar firm.
  • Experience working with digital validation platforms, laboratory information management system integrations, or process-management tools.

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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