Expertise of Finish goods testing. Stability, RM Analytical Method Validation, Dissolution, HPLC, PMQC and knowledge of handle other sophisticated instruments like GC, XRD, ICPMS, LCMS.
For paper studies, ensures all CRFs and DCFs received are returned for filing in the Document Control Room per the Data Tracking Guidelines for the assigned projects.
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Master in Life Sciences, pharmaceutical sciences, animal sciences, biotechnology, microbiology, MVSc with NET, GATE or other national level examination conducted by Central Government departments like DBT, DST or equivalent
M.Sc. Medical Sciences, Pharm.D, BDS, MPH. Prior experience in field work or project management in medical research or experience in Pulmonary function testing
Responsible for process validation and cleaning validations and respective documentation. Responsible for Equipment and utilities qualification and periodic validation.
Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented and performance driven people. All of which makes them one of the most rewarding employers in their field.
Post : Team Lead Medical Communications (Scientific Engagements)
Liaise with key partners, including Pfizer Country Organizations, Clinical Development, License Partners, and other stakeholders regarding safety data collection and data reconciliation.