Key Responsibilities & Accountability – Handled Individually1. Development of Inhalation Dosage Forms: Independently plan and execute formulation developmentof Nasal Spray, Solutions, Suspensions, Drops etc. including single and combination products.2. Selection of the compatible excipients based on their properties as required in such formulations.3. Selection of suitable devices for such formulations.4. Pre-formulation Studies: Evaluate API and excipient characteristics such as particle size distribution,morphology, density, moisture content, flow properties, crystallinity, hygroscopicity etc.5. Particle Engineering Strategy: Detailed understanding of morphology, particle size distribution,polymorphism and other essential physical properties of the drug substances.6. Deep understanding of the process variables for lab-scale and scale-up: Develop and optimizeprocesses considering mixing time, speed, fill weight, segregation risk, content uniformity &viscosity; of the formulation.7. Device–Formulation Compatibility: Evaluate compatibility of the formulation with differentdevices/pumps and optimize formulation considering device resistance and aerosolizationcharacteristics.8. Product Performance Evaluation: Interpret critical performance data including:a. Delivered Dose Uniformity / Uniformity of Delivered Doseb. Droplet Size Distribution (DSD)c. Plume Geometryd. Spray Patterne. Device retention/deposition9. Reference Product Characterization: Conduct systematic characterization of reference/marketedproducts to understand formulation, device, physical characteristics, and critical performanceattributes for generic product development.10. QbD-Based Development: Define and evaluate QTPP, CQAs, CMAs, and CPPs and apply riskassessment, Design of Experiments (DoE), and scientific principles during formulation/processoptimization.11. Stability Studies: Plan and evaluate stability studies and investigate the impact of temperature,humidity, moisture uptake, packaging,



and physical on product performance.12. Technology Transfer: Execute formulation and process transfer from R&D; to pilot/commercialmanufacturing sites and provide technical support during scale-up, exhibit/registration, validation,and commercial batches.13. Troubleshooting: Candidate should have experience related to troubleshooting.14. Documentation: Prepare and review development reports, BOM/MFR, product development reports,technology-transfer documents, protocols, risk assessments, QbD documents, and regulatory-supportdocumentation.15. Literature & Patent Evaluation: Conduct scientific literature, innovator-product, regulatory, andpatent searches to support formulation strategy and identify potential development or patentabilityopportunities.

Secondary ResponsibilitiesCoordinate with ADL for development and interpretation of specific analytical and performancetesting, particularly DSD, Plume geometry, Spray Pattern, Viscosity, Delivered Dose Uniformity.2. Prepare and monitor various protocol bound studies like in-use stability study, photostability study,device-compatibility study.3. Maintain accurate and contemporaneous Laboratory Notebooks (LNBs), experimental records,development data, and material accountability.4. Support preparation of samples and documentation for stability, exhibit batches, BE/PK/clinicalstudies, regulatory submissions, and comparative in-vitro studies
Soft Skills required:1. Scientific & Analytical Thinking: Ability to correlate formulation variables, powder properties,device characteristics, and aerodynamic performance.2. Problem-Solving: Positive problem-solving skills will be desired.3. Ownership & Execution: Ability to independently manage assigned development activities withindefined project timelines.

Education & Qualification1. Education: M. Pharm in Pharmaceutics2. Experience: 4-6 years of relevant experience in Formulation & Development, preferably withsignificant hands-on exposure to Nasal Spray/Solutions/Suspensions/Drops product development

📌 L 5 - Ndds/Tt (Pune)
🏢 Sava Healthcare
📍 Pune