Vaishnavi Akade

M. Pharm. Pharmaceutics

Talent

LaturMember since August 19, 2026

Formulation DevelopmentControlled Drug ReleasePharmaceutical InstrumentationDissolution TestingDrug Regulatory Affairs (DRA)Pharmaceutical Quality ControlPharmaceutical SciencesIn-vitro Drug Release StudiesNanoprecipitationEmulgel technologyParticle size analysisEncapsulation efficiencyRheological studies

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Formulation DevelopmentControlled Drug ReleasePharmaceutical InstrumentationDissolution TestingDrug Regulatory Affairs (DRA)

About

Results-driven Pharmaceutics Professional with over 3 years of experience in the formulation and evaluation of advanced drug delivery systems, including polymeric nanoparticles and pH-sensitive hydrogels. Proficient in preclinical formulation research, with in-depth knowledge of Nano formulation techniques such as nanoprecipitation and emulgel technology for controlled drug release applications. Skilled in operating and interpreting data from pharmaceutical instrumentation including FT-IR, UV-Vis Spectrophotometer, Dissolution and Disintegration Apparatus, Lyophilizer, and Rotary Tablet Compression Machines, HPLC.

Expertise in formulation characterization techniques including particle size analysis, encapsulation efficiency, rheological studies, and in vitro drug release profiling under simulated physiological conditions. Published researcher in peer-reviewed journals, contributing to pharmaceutical sciences literature on targeted drug delivery and phytochemical-based therapeutics, with two first-author publications in 2024. Adept at academic delivery and curriculum development as an Assistant Professor, mentoring undergraduate students and delivering conceptual clarity through structured lectures, workshops, and seminars in core pharmaceutics.

Certified in Drug Regulatory Affairs, with a strong understanding of GMP, GLP, cGMP documentation, compliance, and quality assurance in alignment with national and international pharmaceutical regulatory frameworks. Highly organized and analytically inclined, with proven competencies in project execution, laboratory management, technical reporting, and collaborative research aligned with the dynamic needs of the pharmaceutical industry and academia.

Experience

Assistant Professor at Tatyaraoji More college of Pharmacy (2023-02 – Present)

Developing and delivering engaging lectures, seminars, and tutorials in Pharmaceutics, ensuring alignment with academic standards and student learning outcomes.
Mentoring undergraduate students on academic progression, research orientation, and career development pathways, fostering a culture of continuous improvement.
Participating in departmental meetings, faculty committees, and institutional academic initiatives, contributing to policy formulation and curriculum enhancement.
Promoting interactive learning methodologies and fostering critical thinking among students through structured teaching approaches and individual support.
Supporting departmental goals by engaging in quality assurance processes, accreditation preparation, and collaborative academic planning.
Conducting robust preclinical and in-vitro drug release studies using FTIR, UV-Vis, and dissolution testing methodologies to establish controlled release profiles and ensure pharmacokinetic efficacy.
Driving R&D initiatives focused on novel formulation development while aligning with Drug Regulatory Affairs (DRA) guidelines to maintain pharmaceutical quality control and regulatory readiness.
Delivering advanced academic instruction in pharmaceutical sciences while mentoring students on analytical techniques and hands-on operation of cutting-edge pharmaceutical instrumentation.