Lead AI Engineer (Agentic Systems, Pharma domain)

TalentXO

Bengaluru

Hybrid

INR 4,000,000 - 7,000,000

Full time

5 hours ago
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Benefits offered by this job

Hybrid work flexibility
Immediate joiner

Job summary

TalentXO Bengaluru-based lead AI engineer role focusing on architecting agentic pipelines for pharma data platforms. You will own subsystem designs, build production RAG pipelines, and ensure regulatory compliance (GxP, 21 CFR Part 11) while driving observability and CI/CD.

Immediate joiner preferred in a hybrid setup with in-office collaboration. Role requires hands-on experience with multiple agentic frameworks, Python excellence, and cloud/deployment skills across AWS/Azure/GCP.

Qualifications

  • 6+ years of software or ML engineering with recent 2+ years shipping production LLM/agentic AI in pharma domain.
  • Hands-on proficiency with at least two agentic frameworks (LangGraph, LangChain, AutoGen, CrewAI) and debugging internals.
  • Direct SDK experience with Claude/OpenAI/Vertex AI and tools API usage.
  • Expert Python with production-quality code, typing, tests, packaging, and profiling.
  • RAG pipeline depth with embedding models, vector stores, and evaluation harnesses.
  • Cloud deployment with AWS/Azure/GCP; Docker, Kubernetes, IaC (Terraform/CDK); CI/CD pipelines.
  • Agent observability experience (LangSmith, Helicone) for latency, cost, quality diagnostics.
  • Hybrid work capability; immediate joiner; role is hybrid with limited WFH.

Responsibilities

  • Design and implement complex agentic pipeline components and topology.
  • Own subsystem designs: data flows, API contracts, and failure handling.
  • Lead production RAG pipelines: ingestion, chunking, embeddings, search, latency tuning.
  • Integrate pharma data platforms via REST / event-driven patterns.
  • Own observability and evaluation harnesses for components.
  • Lead CI/CD for modules: containerisation, tests, staging gates, rollbacks.
  • Translate pharma analytics demands into component specs.
  • Ensure 21 CFR Part 11, HIPAA, and GxP traceability in designs.
  • Develop document processing pipelines for pharma content.
  • KOL mapping, competitive intelligence, signal detection agents.
  • Act as technical reference for AI Engineers; review design & unblock issues.
  • Run design reviews and surface architecture risks pre-staging.
  • Mentor juniors and document patterns in knowledge base.
  • Represent engineering quality in client discussions; translate trade-offs clearly.
  • Contribute guardrail templates to internal AI playbook.

Skills

Agentic systems architecture
Python
Production LLM / agentic AI
Frameworks: LangGraph / LangChain / @
Debugging framework internals
Docker / Kubernetes
CI/CD pipelines
Observability (LangSmith / Helicone)
Regulated pharma data handling
Component design specifications
Hybrid work / immediate joiner

Tools

LangGraph
LangChain
AutoGen
CrewAI
Pinecone
Weaviate
pgvector
AWS
Azure
GCP
Terraform
CDK
Docker
Kubernetes
LangSmith
Helicone
IQVIA / Symphony / Veeva integrations

Job description

Design and implement complex components of agentic pipelines — multi-agent graphs, tool orchestration layers, retrieval modules, and memory systems — using LangGraph, AutoGen, CrewAI, or equivalent

Take ownership of full sub-system designs: define agent topology, data flows, API contracts, and failure handling for a bounded scope

Build and optimise production RAG pipelines: document ingestion, chunking strategy, embedding selection, hybrid search, retrieval evaluation, and latency tuning

Integrate agentic systems with pharma data platforms (IQVIA, Symphony, Komodo, Veeva) via REST, event-driven hooks, and batch pipeline patterns

Own observability for components: instrument trace logging, cost metrics, drift alerts, and evaluation harnesses using LangSmith, Helicone, or equivalent

Lead CI/CD for owned modules: containerisation (Docker/Kubernetes), automated test suites, staging gate criteria, and rollback procedures

Translate medical affairs, commercial analytics, and clinical ops requirements into agent component specifications

Apply 21 CFR Part 11 auditability, HIPAA-compatible data handling, and GxP traceability patterns to every component

Build intelligent document processing pipelines for pharma content: drug labels, clinical study reports, HEOR dossiers, and regulatory submissions

Contribute to KOL mapping, competitive intelligence, and signal detection agents with domain-aware retrieval and reasoning strategies

Serve as the day-to-day technical reference for AI Engineers on the pod: code review, design feedback, unblocking implementation issues

Lead component-level design reviews and surface architecture risks before they reach staging

Pair with junior engineers on hard problems and document patterns and decisions in the team's shared knowledge base

Represent engineering quality in client-facing technical discussions and translate complex trade-offs into plain language

Contribute reference implementations and guardrail templates to the firm's internal agentic AI playbook

Role is based in Bengaluru

Immediate joiner required — must be able to start within the next week

Role is within pharmaceutical and life sciences industry context

Roles & Responsibilities
  • Design and implement complex components of agentic pipelines — multi-agent graphs, tool orchestration layers, retrieval modules, and memory systems — using LangGraph, AutoGen, CrewAI, or equivalent
  • Take ownership of full sub-system designs: define agent topology, data flows, API contracts, and failure handling for a bounded scope
  • Build and optimise production RAG pipelines: document ingestion, chunking strategy, embedding selection, hybrid search, retrieval evaluation, and latency tuning
  • Integrate agentic systems with pharma data platforms (IQVIA, Symphony, Komodo, Veeva) via REST, event-driven hooks, and batch pipeline patterns
  • Own observability for components: instrument trace logging, cost metrics, drift alerts, and evaluation harnesses using LangSmith, Helicone, or equivalent
  • Lead CI/CD for owned modules: containerisation (Docker/Kubernetes), automated test suites, staging gate criteria, and rollback procedures
  • Translate medical affairs, commercial analytics, and clinical ops requirements into agent component specifications
  • Apply 21 CFR Part 11 auditability, HIPAA-compatible data handling, and GxP traceability patterns to every component
  • Build intelligent document processing pipelines for pharma content: drug labels, clinical study reports, HEOR dossiers, and regulatory submissions
  • Contribute to KOL mapping, competitive intelligence, and signal detection agents with domain-aware retrieval and reasoning strategies
  • Serve as the day-to-day technical reference for AI Engineers on the pod: code review, design feedback, unblocking implementation issues
  • Lead component-level design reviews and surface architecture risks before they reach staging
  • Pair with junior engineers on hard problems and document patterns and decisions in the team's shared knowledge base
  • Represent engineering quality in client-facing technical discussions and translate complex trade-offs into plain language
  • Contribute reference implementations and guardrail templates to the firm's internal agentic AI playbook
  • Role is based in Bengaluru
  • Immediate joiner required — must be able to start within the next week
  • Role is within pharmaceutical and life sciences industry context
Requirements
  • Strong Lead AI Engineer Profile with agentic systems architecture expertise and pharma regulated-environment experience
  • Mandatory (Experience 1): Must have 6+ years of software or ML engineering, with at least recent 2+ years building and shipping production LLM or agentic AI systems in pharma domain
  • Mandatory (Tech skill 1): Must have hands‑on proficiency with at least two agentic frameworks (LangGraph, LangChain, AutoGen, CrewAI), with experience debugging framework internals
  • Mandatory (Tech skill 2): Must have direct SDK experience with Anthropic Claude API (tool use, streaming), OpenAI Assistants API, or Vertex AI Agent Builder
  • Mandatory (Tech skill 3): Must have Python mastery — production‑quality code, type annotations, unit and integration tests, packaging, and performance profiling
  • Mandatory (Tech skill 4): Must have RAG pipeline depth — embedding model selection, vector stores (Pinecone, Weaviate, pgvector), hybrid retrieval, RAGAS or custom evaluation harnesses
  • Mandatory (Tech skill 5): Must have cloud deployment experience with AWS, Azure, or GCP; Docker, Kubernetes, IaC basics (Terraform or CDK), and CI/CD pipelines
  • Mandatory (Tech skill 6): Must have agent observability experience — LangSmith, Helicone, or equivalent — with ability to diagnose latency, cost, and quality issues in production traces
  • Mandatory (Tech skill 8) : Must have owned full sub‑system designs — agent topology, data flows, API contracts, failure handling — for a bounded scope, and built multi‑agent graphs, tool orchestration, retrieval, and memory systems.
  • Mandatory (Tech skill 7): Must have track record of shipping 2+ agentic or ML systems to production — not just proof‑of‑concepts — with documented performance benchmarks
  • Mandatory (Domain 1): Must have working knowledge of pharma commercial data (Rx/claims, NPI‑level analytics, brand performance metrics) and experience operating in regulated data environments (GxP, 21 CFR Part 11, HIPAA‑compliant data handling)
  • Mandatory (Domain 2): Must have exposure to at least one of: medical affairs analytics, RWE, clinical operations data, HEOR/market access, or regulatory intelligence
  • Mandatory (Communication): Must be able to write crisp component specifications and communicate architectural trade‑offs to both engineers and non‑technical stakeholders
  • Mandatory (Availability): Must be an immediate joiner or currently serving notice period, able to start within the next week
  • Mandatory (Note 1) : Role is Hybrid, WFH flexibility as well upto 6 days a month
  • Mandatory (Note 2): CTC is inclusive of 10% variable
  • Preferred (Tech skill 1): MCP (Model Context Protocol); Veeva Vault, Medidata, IQVIA, or Symphony Health integrations; knowledge graphs (Neo4j, Amazon Neptune); RLHF/fine‑tuning/model adaptation; prior consulting / services‑firm delivery experience

Experience: 6–9 years · Hybrid, 4 days in office · 5 days a week · Notice period less than 15 days

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