MSc, M.Tech, M.Pharm. in relevant stream of Biological Sciences with 3-5 years of relevant experience in Analytical R&D, QC department of Biopharmaceutical industry.
BS, RN, MS, PharmD in life sciences or equivalent relevant scientific qualifications or professional training. Generate and file data for signal detection and safety data review. Demonstrated understanding of global pharmaceutical drug development and lifecycles.
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
VBPL is an ISO 13485:2012 and WHO – GMP certified leading global player in Biopharma sector having more than 15 years of operational experience, situated at Hyderabad. We also have offices located in USA. Innovative, ever motivated Research team and uncompromising manufacturing team in providing quality products are our strengths.
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.