DeepForrest AI
Website:
deepforrest.ai
Job details:
Company Description
DeepForrest AI is revolutionizing how life sciences teams operate by developing AI solutions that are reliable, scalable, and tailored for regulated environments. Our flagship product, Harmony, streamlines Regulatory Affairs by enabling swift dossier authoring and lifecycle management to accelerate compliance processes. Additionally, our products advance quality investigations and enhance pharmacovigilance automation, driving measurable improvements in the life sciences industry. Utilizing human-in-the-loop AI and adhering to 21 CFR Part 11 and global compliance standards, we deliver innovative, responsible, real-world AI solutions that empower the future of life sciences.
Role Description
This is a full-time, on-site role for a Regulatory Affairs Consultant located in Hyderabad. In this role, you will be responsible for developing and implementing regulatory strategies, preparing and submitting regulatory dossiers, and ensuring compliance with relevant global standards and guidelines. You will collaborate with cross-functional teams, monitor regulatory changes, and provide expert guidance to drive timely approvals and compliance. Your work will directly contribute to accelerating product time-to-market while maintaining the highest quality and compliance standards.
Qualifications
- Expertise in Regulatory Strategies, Regulatory Compliance, and understanding of global regulatory requirements
- Experience with Dossier Authoring, CTD/eCTD submissions, and handling lifecycle management documentation
- Proficiency in Monitoring Regulatory Changes and interpreting their impact on ongoing projects
- Strong Collaboration and Communication Skills to work effectively with cross-disciplinary teams and stakeholders
- Bachelor’s or Master’s degree in Life Sciences, Pharmaceuticals, or related fields
- Familiarity with AI solutions for life sciences is a plus
- Highly organized with attention to detail and ability to work under tight deadlines
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