Job Title: Formulation Scientist
– Transdermal Drug Delivery Patch Development
Department: Research & Development (Pharmaceutical Formulations)
Location: [SINE IIT Bombay]
Reports To: Head – Formulation Development
Position Overview
The organization seeks an accomplished Formulation Scientist with a proven track record in transdermal drug delivery systems. The successful candidate will play a key role in the research, design, development, and scale-up of transdermal patch formulations for innovative therapeutics.
Key Responsibilities
Lead the development and optimization of formulations for various transdermal patch types, including matrix, reservoir, adhesive, and multilayer systems.
Conduct pre-formulation studies, assessing drug–polymer–excipient compatibility and physicochemical properties.
Employ statistical tools and Design of Experiments (DoE) for formulation and process optimization and stability assessment.
Prepare comprehensive product development reports, batch manufacturing records, and technical documentation for regulatory submissions.
Oversee scale-up activities and technology transfer to manufacturing units, ensuring robust process reproducibility.
Coordinate with analytical teams to evaluate and validate analytical methods relevant to transdermal systems.
Design and execute in vitro release, permeation, and adhesion studies aligned with ICH and regulatory standards.
Maintain up-to-date knowledge of regulatory trends, ICH guidelines, and advancements in transdermal drug delivery technology.
Participate in patent drafting, conduct literature searches, and contribute to innovation-driven projects.
Required Qualifications & Skills
M.Pharm or Ph.D. in Pharmaceutics, Pharmaceutical Technology, or a related discipline.
3–5 years of hands-on experience exclusively in transdermal patch formulation.
In-depth understanding of polymer science, drug release kinetics, and adhesive technologies.
Experience in operating formulation equipment (coating machines, laminators, dissolution/permeation cells).
Familiarity with cGMP, QbD principles, and regulatory standards for topical and transdermal products.
Exceptional analytical, documentation, and project management skills.
Preferred Attributes
Experience preparing submission-ready regulatory dossiers for US/EU and other regulated markets.
Exposure to advanced delivery systems (e.g., microneedle patches, iontophoretic technologies).
Strong collaborative skills for cross-functional projects involving formulation, analytical, and process engineering teams.
Apply here
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Email- DREPTO BIODEVICES PVT. LTD.|| Rohit Srivastava||