Regulatory AI and Content Specialist at Roche
The Roche Regulatory AI job offers professionals in regulatory affairs an opportunity to join Roche as a Regulatory AI and Content Specialist in Hyderabad. This full-time position is open for applications until 07 October 2026, offering a unique opportunity to contribute to innovative healthcare solutions.
About the Company
Roche is a global healthcare company operating in the pharmaceutical and diagnostics sectors. With a mission to improve lives through innovative solutions, Roche is dedicated to advancing science and ensuring access to healthcare for all. The organization fosters a culture of personal expression and collaboration, allowing employees to thrive both personally and professionally.
Job Details
- Company: Roche
- Location: Hyderabad
- Job Type: Full-time
- Posted On: Today
- Application Deadline: 07 October 2026 (12 hours left to apply)
- Job Requisition ID: 202609-123378
Roche Regulatory AI Job: The Position
As a Regulatory AI & Content Specialist, the successful candidate will bridge Pharma Development Regulatory (PDR), content management, and AI-enabled technology. This role involves leveraging knowledge of regulatory documents and submission requirements to optimize regulatory content for AI-powered authoring and automation. The specialist will also support document authors in drafting regulatory documents, ensuring high quality and compliance.
Key Responsibilities
- Have a strong understanding of regulatory documents across the drug development lifecycle, including clinical, non-clinical, CMC, and CTD-based submissions.
- Apply knowledge of Generative AI, structured content, and regulatory authoring principles to support AI-enabled content creation and document standardization.
- Stay current with evolving regulatory requirements, AI capabilities, and industry best practices.
- Analyze regulatory documents and convert them into standardized templates and reusable content components.
- Configure and maintain templates, metadata, and content assets for efficient regulatory authoring.
- Serve as a super user for the GenAI-powered platform, providing business support and user enablement.
- Participate in User Acceptance Testing (UAT) and collaborate with stakeholders to align regulatory content with business needs.
- Identify opportunities to improve regulatory content development through AI and automation.
Eligibility Criteria
- Bachelor’s or Master’s degree in Life Sciences, Pharmacology, Regulatory Affairs, or a related discipline.
- 4–6 years of experience in Regulatory Affairs, Regulatory Operations, Regulatory Writing, or a related pharmaceutical role.
- Experience in leading or supporting clinical or marketing authorization submissions.
- Ability to critically review and interpret regulatory documents and translate them into structured content.
- Knowledge of Generative AI and digital technologies relevant to regulatory processes.
- Experience with structured content authoring and document templating.
- Excellent analytical, written communication, collaboration, and stakeholder management skills.
How to Apply
Interested candidates can apply for the position through the following link:
CLICK HERE FOR THE ORIGINAL NOTIFICATION / APPLY ONLINE
This Roche regulatory AI role presents a significant opportunity for qualified individuals to contribute to the advancement of healthcare through innovative regulatory practices. Interested candidates are encouraged to apply before the deadline on 07 October 2026.
