Hyderabad

Overcoming the Inflammatory Cascade in Neonatal Sepsis, a Nanomedicine Approach. First class post-graduate PG degree including integrated PG degree such as M.S. Pharm, M.Pharm, M.Sc, M.Tech or Equivalent with specialization in Pharmacology & Toxicology, Regulatory Toxicology, Biotechnology, Life Sciences.

Assistant Professor Pharmaceutical Management recruitment at NIPER; Ph.D. with 1st Class or equivalent at the preceding Degree in an appropriate branch with a good academic record throughout and at least 5 years of teaching/research, industrial experience with published works of high quality

Bachelors or Masters degree in Pharmacy, Pharmaceutical Sciences. Lead and manage the technology transfer of pharmaceutical formulations from R&D to manufacturing Collaborate with cross-functional teams including R&D, Quality Assurance, Regulatory Affairs

BPharm or MPharm require; Review of Protocols and reports related to Analytical method validation, Verification of API and Finished product, Vendor qualification, cleaning validations. Hypothesis analysis, general validations, Stability, photo stability, thermal cycling, in use, split study and miscellaneous studies and approval in LIAAS where ever applicable.

Lead Writer for simple submissions, contributing to key messaging and pooling strategy, providing content guidance, and ensuring compliance of documentation to internal company standards and external regulatory guidelines.

Risk-based monitoring is an adaptive approach to clinical trial monitoring that directs focus and activities to critical data and processes that have the most potential to impact patient safety and data quality.

Bachelor, Masters Degree with experience in Pharmaceutical Industry; Acts as a single point of responsibility for application for ensuring the system and data are secured as required by Information Security and Compliance requirements.

Lead active surveillance and analysis of emerging regulations, perform impact assessments and drive process changes required to ensure ongoing compliance to global regulatory requirements. Analyze the impact of other Novartis processes and organizational changes on assigned processes.