M.Pharm

Exposure to aseptic process activities, aseptic techniques, aseptic filling and sealing activities, and media filling activities. Experience in operating autoclaves and terminal sterilizers. Preparation of autoclave loads, loading and unloading of autoclaves and sterilizers

The International Conference on Translational & Technological Advances in Health Sciences ICTAHS-2025 is set for Nov 13-15, 2025

Phase 2 Pilot Study to test the efficacy of Ayurvedic oral cannabis preparation in the peri-operative Period in oral cavity squamous cell cancer. Post Graduation in Science M.Pharm, Life Sciences, Biotech, Zoology, etc with PG Diploma in Clinical Research is mandatory, with one year experience in relevant filed is preferred.

Preparation of sugar-free Unani formulation and its comparison with the Unani drug for their immunomodulatory potential against the in vivo model of maniac phase of bipolar disorder. M.Pharm / M.Sc in Life Sciences / Biotechnology. 

Development of Microneedle Array Patch Based Haemophilus Influenza Type-B Hib Vaccine Delivery System for Improved Logistics and Better Patient Compliance. First class M.Pharm, M. S. Pharm in Pharmaceutics Pharmaceutical analysis and Pharmacology also will be considered with GATE, GPAT, CSIR UGC-NET including lectureship or equivalent examination.

Certification in clinical research analysis is advantageous but not mandatory. Willingness to learn regulatory compliance is a must. Candidate with evidenced experience in clinical trial, relevant data analysis, data management and clinical statistical analyses will have additional weightage in selection.

The ideal candidate will be responsible for compiling Drug Master Files DMFs and Certificates of Suitability CEPs, ensuring compliance with global market regulations and emerging market standards in accordance with ICF guidelines. This role requires strong coordination with internal stakeholders and expertise in regulatory submissions, amendments, and annual reports.

Define and implement the formulation development strategy, aligning with the broader RAD and business objectives. Lead the preparation of development reports, protocols, and documentation required for regulatory submissions. Identify and implement cutting-edge formulation technologies for new drug delivery systems. Ph.D / M.Pharm, Formulation Development NCE, Medicinal Chemistry

M.Sc / B.Pharm / M.Pharm; Computerized System Validation CSV, MES, Equipment Qualification; RM/PM, Dispensing, Inspection