Roche Posted September 12, 2026

Regulatory AI & Automation Specialist

Hyderabad, Telangāna, India FULL_TIME
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Roche is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.

The Position

Role: Regulatory AI & Automation Specialist

Location: Hyderabad

Job Type: Full Time

Years of Experience: 4–6 years

A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love.

That’s what makes us Roche.

Mission

Roche Services & Solutions (RSS) aims at "transforming the way Roche operates.'' As a global organization of over 3,500 colleagues, we enable Roche to operate in a competitive and ever-changing business environment. We provide our partners with end-to-end business services and solutions, enabling them to focus on patient-centric activities. Embracing an OneRoche mindset, we leverage our global network located in Budapest (Hungary), Riga (Latvia), Chennai & Hyderabad (India), San José (Costa Rica), Kuala Lumpur (Malaysia), and our other sites to remain customer-centric 24/7 and co-create solutions together.

The PD Regulatory Innovation and Sustainment Chapter is accountable for creating and maintaining a framework for building, maturing, and sustaining PDR business capabilities. This includes fostering innovation, ensuring operational readiness, and implementing continuous improvement across our regulatory processes, systems, and tools. Chapter members lead by designing and deploying innovative, compliant solutions that optimize regulatory workflows while maintaining the highest standards of integrity and data quality. We operate with enterprise thinking in a highly transformative regulated environment, assessing end-to-end processes, anticipating regulatory landscape changes, and unlocking company-wide benefits through strategic partnerships across PD, affiliates, Pharma, and the Roche group. Success in this chapter requires strategic thinking, systems thinking, data and content management expertise, an enterprise mindset, and the ability to drive continuous improvement and change leadership in a matrix environment.

Your Opportunity

As a Regulatory AI & Automation Specialist within PD Regulatory Innovation and Sustainment Chapter at RSS Hyderabad, you will drive the hands-on digital execution of regulatory operations. In this role, you will design, build, and deploy AI-driven tools, document intelligence engines, and automated workflows that accelerate regulatory document processing, submission dossier management, and compliance tracking across global health authorities

Key Responsibilities:

Collaborate with regulatory stakeholders to evaluate incoming AI/automation requests, assess technical feasibility, and help prioritize high-value use cases for regulatory document workflows.

Build and deploy scalable AI, machine learning, and automation solutions, integrating RPA, Low-Code/No-Code platforms, Python, NLP, and cloud-native services like AWS, specifically tailored to optimize global regulatory workflows and document management.

Perform operational process mining and opportunity mapping by partnering directly with SMEs from PDR Innovation & Sustainment chapter and global regulatory SMEs to identify high-impact AI and automation opportunities.

Support IT team by providing business directions for ongoing technical & preventive maintenance, performance monitoring, and troubleshooting for all deployed automation scripts, machine learning models, and AI assets operating in production.

Maintain comprehensive technical artifacts (including solution architecture, source code repositories, and testing frameworks) and conduct hands-on internal training to empower business teams and drive adoption across global regulatory functions.

Drive cross-functional Agile and DevOps execution in a matrixed environment, collaborating with PDR Innovation & Sustainment chapter leads, regulatory teams, IT, and RSS peers through sprint planning, rapid PoC prototyping, iterative testing, and continuous feedback loops.

Monitor operational performance metrics and deliver clear project updates, technical insights, and continuous improvement recommendations to functional leadership and regulatory stakeholders.

Partner with global regulatory teams to showcase the practical applications of AI, NLP, and automation, translating technical features into clear business benefits like compliance risk reduction, improved document processing throughput, and operational efficiency.

Who You Are

You are a hands-on technical builder with 4–6 years of experience in software engineering, data analytics, or AI/automation development and exposure of working in pharmaceutical R&D regulatory affairs or clinical development departments. You possess strong analytical problem-solving skills and thrive in an agile setting where you take ownership of technical execution, turning complex operational processes into automated, production-ready AI tools.

Qualifications & Technical Skillset:

Education & Experience: Bachelor’s or Master’s in Computer Science, Data Science, Information Technology, Statistics, or a related quantitative field, with 4–6 years of hands-on experience building and deploying software, automation, or AI/ML solutions

Education & Experience: Direct experience in pharmaceutical R&D regulatory affairs or clinical development.

Advanced GenAI: Experience exposure to prompt evaluation frameworks, or multi-agent orchestration.

Core Programming & Data Engineering: Advanced proficiency in Python and SQL for data extraction, manipulation, pipeline creation, and writing modular, production-ready code.

Document AI & Text Processing: Practical experience with Natural Language Processing (NLP), Optical Character Recognition (OCR like Tesseract, AWS Textract, or Azure AI Document Intelligence), and unstructured document parsing (PDFs, XML, JSON, Word).

AI & LLM Integration: Hands-on experience developing application logic around modern LLM frameworks (e.g., Lang Chain, Llama Index, OpenAI/AWS Bedrock APIs) and building Retrieval-Augmented Generation (RAG) pipelines for document querying.

Software Engineering & APIs: Solid experience with REST APIs, Git version control, unit testing, and basic CI/CD practices.

Workflow & Process Automation: Experience automating workflows using Python orchestration, low-code automation tools (e.g., Power Automate, UiPath), or enterprise schedulers.

Exposure to Deployment & Cloud: Basic exposure to cloud platforms (AWS, Azure) and containerization (Docker) for deploying scripts and API services.

Strong to have:

Prompt Architecture & Validation: Ability to design complex, multi-step prompts; validate outputs against business logic; and refine solutions iteratively.

Regulatory Domain Knowledge: Foundational knowledge of ICH guidelines FDA/EMA submission processes, regulatory document formats (eCTD, GxP guidelines, CT documentation), emerging AI/ML regulatory guidance.

Note: This job description is intended as a general guideline for the responsibilities and qualifications required for this position. It is not an exhaustive list, and responsibilities may evolve and change based on business needs.

 

 

Who we are

A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.

Let’s build a healthier future, together.

Roche is an Equal Opportunity Employer.

Job details

Seniority
Not listed
Function
Regulatory Affairs
Therapeutic area
Not listed
Location
Hyderabad, Telangāna, India
Employment type
FULL_TIME

How this role compares

Computed from every other active Regulatory Affairs role in our database, not just this employer's listings.

We currently track 407 comparable Regulatory Affairs roles across 100 biopharma companies.

407Comparable roles tracked
394Currently active
100Companies hiring similar roles
43Countries represented

Salary context

116 of 407 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Peer group range $115,000 – $380,750 (median $205,000)

Where these roles are based

Top locations among the 407 comparable roles

United States165
India33
Japan28
United Kingdom25
Poland21
Ireland20

+ 37 more countries

Seniority mix

332 of 407 peers have a known seniority level

Manager128
Director64
Associate Director43
Senior38
Intern/Fellow/Postdoc19
Senior Director16
Executive/VP12
Associate9
Principal3

Therapeutic area mix

38 of 407 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology18
Rare Disease7
Immunology4
Vaccines & Infectious Disease3
Dermatology & Aesthetics2
Neuroscience2
Cardiovascular / CVRM2

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The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

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Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

40%
Manager CMC Regulatory Affairs
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Function Therapeutic area Seniority Country
40%
Senior Manager Triage
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Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.