The Regulatory Affairs Senior Associate will work at the interface of R&D; and Regulatory, building a genuine technical understanding of the product's formulation and analytical profile to support sound regulatory strategy. This is not a document-processing role — it requires the ability to engage with development science, identify potential issues, and contribute informed regulatory thinking rather than just administrative submission support. Responsibilities
• Develop a working technical understanding of assigned products — formulation composition and rationale, manufacturing process, and analytical/impurity profile — sufficient to identify regulatory implications independently.
• Review R&D; and Analytical data, including formulation trials, stability studies, method validation and characterization data, critically to spot gaps, inconsistencies or risks.
• Support the Manager/Director in framing regulatory strategy by contributing well-reasoned technical inputs.
• Assess the regulatory impact of significant development changes and ensure that comparability, bridging or additional evidence requirements are addressed prospectively.
• Prepare and/or review assigned dossier sections, briefing packages and responses to major authority questions, ensuring completeness.




• Drive submission readiness, including gap closure, review cycles, issue escalation and completion against agreed milestones. Requirements Experience and Qualifications
• Minimum 4 years of relevant pharmaceutical or biopharmaceutical industry experience.
• Minimum 2-3 years of genuine exposure in R&D;, either formulation development and/or analytical sciences. Required Skills
• Understanding of and hands-on experience with regulatory dossier structure and requirements, including CTD/eCTD, is preferred, though the primary emphasis of this role is technical/scientific understanding over document compilation.
• Strong analytical thinking and the confidence to raise technical concerns proactively.
• Clear written and verbal communication skills for cross-functional technical discussions.
• Ability to manage multiple deliverables independently within defined timelines. Added Advantage
• Experience with complex injectables, biologics/biosimilars, drug-device combination products or other technically complex dosage forms. Benefits The company offers competitive salary and advantages, continuous specialized training, career development and a friendly working environment.

📌 Regulatory Affairs Senior Associate (Hyderabad)
🏢 DEMO Pharmaceuticals
📍 Hyderabad