Ankush Panda
Analytical R&D Professional | Expertise in Analytical Method Development, Validation & Documentation | Transdermal and Oral solid | M.Pharm (Pharmaceutical Analysis)
- Role
- Research Associate at Difgen Pharmaceuticals
- Location
- Hyderabad, TG, IN
- LinkedIn followers
- 500 followers
About Ankush Panda
Detail-oriented Analytical R&D professional with 4.9 years of experience in pharmaceutical analysis, method development, and validation for solid oral and transdermal formulations. Experienced in conducting analytical studies in accordance with GMP, GLP, and GDP standards, and proficient in preparing scientific documentation such as method validation/verification reports, MDRs, standard testing procedures (STPs), and analytical protocols.Skilled in preparation and review of stability data for feasibility and exhibit batches, dissolution development reports, photostability reports. Demonstrated expertise in generating and interpreting analytical data to support product development and regulatory submissions.Currently expanding my expertise into Regulatory Affairs (CMC) to leverage my analytical background in supporting dossier preparation, CTD/ANDA submissions, and compliance documentation. Recognized for strong documentation accuracy, cross-functional collaboration, and a proactive approach toward regulatory readiness and inspection support.Passionate about ensuring data integrity, product quality, and regulatory compliance throughout the pharmaceutical product lifecycle.
Experience
Research Associate
Mar 2024 — Present · Hyderabad, IN
Conducting analytical method development and validation for assay, related substances, dissolution, and residual solvents using HPLC, GC, and UV-Preparing analytical validation protocols and STPs aligned with regulatory standards-Supporting dossier-related analytical data compilation and documentation for regulatory submissions-Ensuring GDP/GLP compliance and readiness for internal and external audits-Reviewed and compiled analytical data for specifications, analytical methods, and validation summaries required for regulatory submissions-Supported regulatory query responses, analytical change controls, and post-approval variation documentation.
Education
College of Pharmaceutical Sciences (CPS), Mohuda, Berhampur
B.pharm, Pharmacy
2016 — 2020
Roland Institute of Pharmaceutical Sciences (RIPS), Berhampur
Master's degree in Pharmaceutical Analysis and quality assurance , Pharmacy
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