ANUBHAV MISHRA

• Serving as Study Director for GLP-aligned preclinical toxicity studies.
• Conducted repeated dose (oral, dermal, IV) and acute toxicity (oral, dermal) studies in rodents and rabbits.
• Supervised animal handling, dosing, necropsy, and data interpretation.
• Conducted 5 toxicity study on rodent and non rodent model
• Coordinated cross-functional teams for protocol preparation, study execution, and report finalization.
• Ensured regulatory compliance per OECD guidelines and GLP.
• Participated in risk assessment and study design optimization for dermal absorption endpoints.

• Conducted inactivation and abnormal toxicity tests for rabies vaccine and Gonadotrophin API/FP in mice and Guinea pigs.
• Analysed in-process samples following SOPs, STPs, GTPs, and protocols.
• Conducted bioassays, RLH, and potency (NIH) tests for rabies vaccine in mice.
• Monitored environmental conditions such as temperature, humidity, and differential pressure.
• Prepared disinfectants, verified cleaning activities, and managed calibration planners.
• Operated, calibrated, verified, qualification and maintained lab instruments and equipment, including autoclaves, dry heat ovens, and dehumidifiers.
• Sent samples for external testing and maintained animal breeding documentation.
• Handled breakdown memos and managed material procurement through SAP.
• Performed statistical analysis using GraphPad Prism and CombiStats.
• Served as training coordinator and QUEST representative within QC team.
• Collaborated with cross-functional teams to optimize workflows and improve productivity.
• Organized and conducted regular training sessions to enhance team skills and knowledge.
• Coordinated with suppliers to establish incoming inspection protocols and ensure raw material quality.
• Provided regular updates to leadership on quality metrics and addressed consistency issues.
• Interpreted test results against specifications and made recommendations for data release.
• Enhanced lab safety through proper protocols and equipment maintenance.
• Contributed to continuous improvement of QC systems through audits and feedback.
• Developed training materials and work instructions for onboarding new team members.
• Conducted root cause analyses for non-conformance reports, leading to proactive problem-solving strategies.
• Ensured compliance with industry standards and kept up-to-date with relevant guidelines and regulations.

Created materials and exercises to illustrate application of course concepts.

• Mentored students and communicated internship and employment opportunities.
• Contributed to departmental goals by serving on various committees focused on curriculum development, assessment strategies, and accreditation requirements.
• Maintained an up-to-date knowledge of subject matter by attending conferences, workshops, and webinars relevant to the field of study.
• Taught courses in Anatomy and Physiology, Pharmacology, and Toxicology to B.Pharmacy students.
• Supervised and mentored students in their academic and research projects, fostering collaborative learning environment.
• Utilized innovative teaching methods and technologies to improve student engagement and learning outcomes.
• Developed and delivered engaging lectures, practical sessions, and assessments to enhance student understanding and performance.
  

• Assist in coordinating oncology clinical trials by managing patient data, ensuring protocol compliance, and supporting the research team with administrative tasks.
• Completed a retrospective observational study on breast cancer patients treated at a single institute from 2013 to 2019. The research analyzed overall survival and progression-free survival, considering factors such as treatment completion, body mass index (BMI), and recurrence rates.