Bengaluru

Demonstrated experience in pharmaceutical, life sciences preferred or healthcare in the data areas of patient or HCP, HCO data, sales and marketing data, financial, or product data.

Project coordination, data collection, field level supervision of data collection, qualitative interviewing, development of IEC materials and networking with local communities and health officials. Patient recruitment, follow-up, communication and interaction.

BPharm/MBBS/Integrated BS-MS/MSc/BE/BTech or equivalent degree. Study of two-dimensional material interfaces for accumulated charge states for molecular interaction for self-powered gas sensor. To carry out experiments, characterizations, preparing reports etc. Instrumentation and Applied Physics, Indian Institute of Science, Bangalore

Participate In activities of literature review. Design and implement comprehensive literature search strategies on specific products. Experience In Patient Safety, solid knowledge In Pharmacovlgllance concepts, regulations and procedures.

Taking the responsibility for bacterial upstream, lysis & Solubilization process. Performing sampling activity during batch processing and updating sampling annexures. Performing pH and conductivity meter calibration, filter integrity test, filtration activity.

To participate in sample processing for PK, ADME assays and handling of LCMS/MS. Ability to adapt to the dynamic team environment. Processing of different matrices samples of PK studies. Optimization of test compounds manually as well as automated on LCMS/MS. M.Pharm in Pharmaceutical sciences, Pharmaceutical Analysis who has interest and passion for LC/MS related bioanalysis

MPhil in Neurophysiology, Neurosciences OR Masters Degree in Neurosciences, Physiology, Life Sciences, M.S Pharm or M. Pharm. in Pharmacology or Biotechnology or equivalent Master’s degree with good academic record

Plans and coordinates activities to ensure regulatory lifecycle management activities and approvals are achieved by the Local Operating Company in a timely manner for all globally approved products.

Create and review regulatory documentation for Drug, Device and Combination product renewals and other life cycle maintenance-related submissions. Track status and progress of regulatory documentation.