Aodh Lifesciences
Website:
aodhlifesciences.in
Job details:
About the Company:
At Aodh Lifesciences, we are building a next-generation deep science drug development company focused on redefining respiratory drug delivery through a regulatory-driven approach. Our work integrates translational biology, microbiology, advanced formulation and device engineering, PBPK modelling, IVIVC modelling, and regulatory-grade data generation to develop targeted therapies designed to improve local efficacy while minimizing systemic exposure and addressing antimicrobial resistance.
We are looking for driven individuals who are curious, think deeply about the science, and are excited to take ownership in a zero-to-one environment, building not just products but a globally relevant, regulatory-grade R&D ecosystem from the ground up.
Roles and Responsibilities
• Evaluate upper airway indications, especially sinusitis, from the perspective of anatomy, physiology, etiology, disease mechanisms, and local delivery barriers.
• Identify and define correct target regions for drug deposition and action in the nasal cavity and sinonasal system.
• Study and document factors affecting local delivery: mucociliary clearance, mucus properties, airflow pathways, inflammation, obstruction, edema, discharge, and disease-state variability.
• Assess differences between acute vs. chronic disease, and post-surgical or altered sinonasal anatomy where relevant.
• Convert biological and anatomical understanding into product design inputs for formulation, device, performance characterization, and microbiology teams.
• Define target zones, avoid zones, delivery barriers, patient-use variables, and stress-case scenarios (congestion, high mucus load, septal deviation, altered airflow).
• Conduct literature review and evidence synthesis from publications, guidelines, patents, product labels, and regulatory documents.
• Prepare regulatory-style documents: indication dossiers, target-zone requirement documents, scientific justification notes, upper airway biology reports.
• Build and maintain a structured knowledge base of upper airway anatomy, physiology, and etiology for current and future products.
• Coordinate with pharmaceutics, microbiology, regulatory/documentation, and management to keep the product at the centre.
• Support scientific interactions with CROs, consultants, and testing labs — briefing, query resolution, and interpreting outsourced outputs.
• Contribute reusable frameworks, templates, assumptions registers, and decision-oriented documentation to the broader delivery platform.
Qualifications
• Pharmacology (postgraduate/ PhD)
• PhD in a relevant life sciences, pharmaceutical sciences, or biomedical discipline
• BDS
• M.Pharm (Master of Pharmacy) & Pharma.D
• Prior exposure to nasal, sinonasal, respiratory, or ENT product development is a plus, not mandatory
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