Senior AI Engineer

Heptarc; India; Hybrid; INR 2,500,000 - 4,000,000; Full time

Job summary

Heptarc is seeking a Senior AI Engineer in Hyderabad with 5–10 years of experience to design, develop, and deploy enterprise AI solutions using Microsoft Azure AI Services, Azure OpenAI, Copilot Studio, and Generative AI technologies.

The ideal candidate will bring strong Life Sciences regulatory affairs domain expertise, and will lead AI initiatives for regulatory submission management, health authority interactions, labeling, pharmacovigilance, quality and compliance functions.

Qualifications

• 5–10 years of AI/ML engineering experience in enterprise settings.
• Experience designing and deploying AI/ML solutions on Azure AI services.
• Strong domain knowledge in Life Sciences regulatory affairs and compliance.
• Practical experience with prompt engineering, RAG, and governance for regulated environments.

Responsibilities

• Lead design and implementation of AI-powered solutions for regulatory submission management and health authority interactions.
• Develop enterprise-grade applications using Azure OpenAI, Azure AI Foundry, and related services.
• Build domain-specific copilots for Regulatory Affairs, Submission Management, Labeling, and Quality & Compliance.
• Collaborate with Regulatory Affairs to map processes and ensure compliance with global standards (GxP, FDA, EMA, ICH).
• Implement AI governance, prompt grounding, and hallucination mitigation strategies.

Skills

AI/ML Engineering

Generative AI

Regulatory affairs

LLM fine-tuning

Tools

Azure OpenAI Service

Azure AI Foundry

Azure Cognitive Services

Azure AI Search

Azure Machine Learning

Azure Functions

Logic Apps

SharePoint

Dataverse

Veeva

Job description

Contract with Client

Location: Hyderabad

Experience: 5 to 10 Years

Mode: Hybrid

Skill: AI/ML Engineering

Job Description: -

We are seeking a highly skilledSenior AI Engineerwith 5 to 10 years of experience in designing, developing, and deploying enterprise AI solutions usingMicrosoft Azure AI Services, Azure OpenAI, Copilot Studio, and Generative AI technologies. The ideal candidate must have strong experience in theLife Sciences and Pharmaceutical Regulatory Affairs domain, with expertise in leveraging AI to streamline regulatory processes, document intelligence, compliance operations, and knowledge management.

The candidate will lead the design and implementation of AI powered solutions supporting regulatory submission management, health authority interactions, pharmacovigilance, labeling, quality, and compliance functions.

Key Responsibilities

AI & Generative AI Development

• Design, develop, and deploy scalable AI/ML and Generative AI solutions on Microsoft Azure.
• Build enterprise grade applications using:
  • Azure OpenAI Service
  • Azure AI Foundry
  • Azure Cognitive Services
  • Azure AI Search
  • Azure Machine Learning
  • Azure Functions and Logic Apps
• Develop Retrieval Augmented Generation (RAG) solutions leveraging regulatory content repositories.
• Fine tune and optimize LLM based applications for regulated pharmaceutical environments.
• Implement prompt engineering, grounding, hallucination mitigation, and AI governance frameworks.

Microsoft Copilot Studio

• Design and develop intelligent agents using Microsoft Copilot Studio.
• Integrate copilots with enterprise systems, SharePoint, Dataverse, Veeva, and regulatory platforms.
• Configure orchestration, actions, workflows, and conversational AI experiences.
• Build domain specific copilots for:
  • Regulatory Affairs
  • Submission Management
  • Labeling
  • Medical Information
  • Quality & Compliance

Life Sciences & Regulatory Affairs

• Collaborate with Regulatory Affairs teams to understand business processes and compliance requirements.
• Develop AI powered solutions supporting:
  • eCTD submissions
  • Regulatory document authoring and review
  • Health Authority correspondence management
  • Labeling content management
  • Regulatory intelligence
  • Change impact assessments
• Ensure compliance with GxP, FDA, EMA, ICH, and global regulatory standards.