Hanumant Bhusnar M. Pharm
Assistant Manager @Endo Pharmaceuticals
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WORK HISTORY
Assistant Manager @Endo Pharmaceuticals
Navi Mumbai, IN
EDUCATION
Marathawadha Mitra Mandal's College of Pharmacy Kalewadi Pune
Master of Pharmacy MMCOP PUNE, Analytical Research and Development
JSPM'S Jaywantrao sawamt college of pharmacy
B. Pharmacy (JSCOP&R)Hadapsar, Pharmacy
ABOUT HANUMANT BHUSNAR M. PHARM
Goal oriented professional with about 13+ years of experience in Analytical Research and Development.• Presently Working with Endo India Par Formulation Private Limited, Mumbai (India) in Analytical Research and Development in Complex injectable, Peptides, Ophthalmic and Inhalation product formulation as scientist on Assistant Manager Position.• Involved in start to end activity analytical research and development from initial phase gate to filing phase gate.• Completed Regulatory Affairs (Medical Device as Major) Industry Certification Course in Institute of Good Manufacturing Practices India (IGMPI) New Delhi with CGPA 7.61.• Led planning and task allocation for analytical method development, routine testing, and stability studies.• Reviewed development reports, stability data, external lab results, and validation documentation.• Participated in cross-functional project meetings to discuss prototype submissions and PDR data.• Collaborated with formulation scientists to resolve analytical challenges by understanding formulation criticality.• Conducted literature reviews (USP, BP, Ph. Eur.) and prepared development strategies for cost-effective, robust methods.• Sourced vendors for APIs, excipients, chemicals, columns, and logistics; obtained quotations for development studies.• Developed and optimized methods for assay, related substances, particle/globule size, viscosity, rheology, osmolarity, buffer capacity, admixture studies, and in-vitro bioequivalence.• Conducting method development for admixture study and content in injectable products on ion chromatogray.• Prepared specifications, STPs, validation protocols, execution reports, and summaries for regulatory filing.• Drafted and reviewed SOPs; ensured compliance and operational efficiency.• Calibrated and operated analytical instruments including HPLC (Agilent, Shimadzu, Dionex, and Waters), UV, IR, and Mass spectrometry.• Characterized drug products and substances using advanced analytical techniques.
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