Intellectt INC
9 months ago
Senior eTMF Product Developer | Hyderabad (Onsite)
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Company information
- Company
- Intellectt INC
- Location
- India, Telangana, Hyderabad, Kyasaram India
- Posted
- 9 months ago
Job description
Title: Senior eTMF Product Developer | Hyderabad (Onsite)
We're building a next-generation eTMF platform for global clinical trials and are looking for a Senior eTMF Product Developer with strong experience in Java, .NET, React, Python, and emerging AI technologies to help shape a Veeva-like, GxP-compliant SaaS product.
Location: Hyderabad (Onsite)
Experience: 7+ years
Industry: Life Sciences / Clinical Research Technology
What You'll Do
Build and scale a commercial eTMF SaaS platform
Develop backend services using Java, .NET, Python
Create modern, responsive UIs with React
Integrate AI/ML capabilities for document intelligence and compliance analytics
Ensure compliance with 21 CFR Part 11, ICH-GCP E6 R2/R3, EU Annex 11, ISO 13485, MHRA GxP
Implement inspection-readiness features aligned with TMF Reference Model
Design APIs and integrations with clinical systems (CTMS, EDC, QMS)
What We're Looking For
5-7 years of product or platform development experience
Strong hands-on experience with Java, .NET, React, Python
Exposure to R and advanced analytics is a plus
Experience with AI/ML or automation technologies
Background in regulated or life sciences software preferred
Product mindset and strong system design skills
Why Join
Build a flagship clinical research product
Work at the intersection of technology, compliance, and AI
We're building a next-generation eTMF platform for global clinical trials and are looking for a Senior eTMF Product Developer with strong experience in Java, .NET, React, Python, and emerging AI technologies to help shape a Veeva-like, GxP-compliant SaaS product.
Location: Hyderabad (Onsite)
Experience: 7+ years
Industry: Life Sciences / Clinical Research Technology
What You'll Do
Build and scale a commercial eTMF SaaS platform
Develop backend services using Java, .NET, Python
Create modern, responsive UIs with React
Integrate AI/ML capabilities for document intelligence and compliance analytics
Ensure compliance with 21 CFR Part 11, ICH-GCP E6 R2/R3, EU Annex 11, ISO 13485, MHRA GxP
Implement inspection-readiness features aligned with TMF Reference Model
Design APIs and integrations with clinical systems (CTMS, EDC, QMS)
What We're Looking For
5-7 years of product or platform development experience
Strong hands-on experience with Java, .NET, React, Python
Exposure to R and advanced analytics is a plus
Experience with AI/ML or automation technologies
Background in regulated or life sciences software preferred
Product mindset and strong system design skills
Why Join
Build a flagship clinical research product
Work at the intersection of technology, compliance, and AI
Required skills
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