B.Pharm/M.Pharm/B.Sc/M.Sc; Production and Packaging, Planning, Monitoring and Reporting production activities. Purchase and procurement planning, monitoring and reporting purchase activities
Clinical Regulatory Writing team provides expert communications leadership to drug projects and authors strategically important clinical-regulatory documents that are label focused and align with project strategies, regulatory requirements, and communications best-practices.
Person should be well experienced in Environment Monitoring of Injcetable facility Settle plate, air sampling, surface monitoring and personnel gown monitoring. He must be aware of good documentation practices and aseptic behavior.
R&D Data Steward plays a critical role in the intersection between business and data, where stewards will guide business teams on how to unlock value from data. This role will drive definition and documentation of R&D data standards in line with enterprise.
The candidate is expected to perform cell biology, molecular biology, biochemistry experiments etc. e.g. cell culture, flow cytometry, immunofluorece imaging, western blotting. RT-PCR experiments annotate and analyse data.
GPAT is a national level examination for award of scholarship to qualified candidates seeking entry into Master of Pharmacy (M. Pharm) course. The first GPAT was conducted in the year 2010 and thereafter it is conducted every year till 2018 by All India Council for Technical Education (AICTE) as per the directions of Ministry of Education, Government of India and from the year 2019, the examination is conducted through the National Testing Agency (NTA) as per the directions of Ministry of Education, Government of India to till 2023.
Project Name Strengthening genomic surveillance for vector borne diseases in India. Post Graduate Degree Virology, Microbiology, including the integrated PG degrees with PhD.
Collecting and submitting in-process samples, finished product samples, stability samples, control samples, cleaning samples, and other samples as per the respective procedures, batch manufacturing records and packing records, protocols. Conducting AQl inspections and periodic inspections of control samples
Ph.D. in Health Sciences with first class or equivalent grade at the preceding degree M.Pharm, M.S, M.Sc, M.D in Pharmacy Practice, Clinical Pharmacy, Clinical Pharmacology, or Clinical Epidemiology with a very good academic record throughout with 2 years of Teaching, Research, Industrial experience with published works of high quality.