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BPharm, BSc, MPharm, MSc, MBBS, BAMS; Experience in PV/ Clinical Research drug safety preferred. Ability to understand and analyses the complex data and performs the activities including accessing the case in Argus, code and enter data.

Experience in Pharmaceutical Company in Parental, responsible for line clearance activity, responsible for in process checks, responsible for sampling. Finished product checking before release, management and execution of process validation & media fill simulation.

Write brief narratives summarizing the ICSR criteria and other potentially safety-relevant information in each article. Demonstrates understanding of client’s drugs labels and uses that knowledge effectively when performing the safety assessments.

OSD - Coating, Compression, Granulation, Ointment-External Preparation General Manufacturing and Sterile Manufacturing. IPQA - OSD and Injectable, AQA, APQR, Documentation, Validation, QMS, CQA, Artwork. Injectable, Aseptic, SIP, CIP, Batch Manufacturing, Bulk Manufacturing, Dry Powder, Oral Liquid. B.Pharm, B.Sc, M.Sc. HPLC Operating, Dissolution, Assay, RS, RM-Testing by HPLC, GLP HPLC Calibration, Finished Product Analysis By HPLC, PM Lab Testing 

B.Sc / M.Sc / B.Pharma / M.Pharma; Review HPLC methods, chromatograms, and system suitability. Ensure HPLC sequences comply with methods. Prepare and review IQ, OQ, and PQ for new instruments. Conduct pre-investigations for OOS, OOC, OOT, and lab incidents. To perform line clearance, FG Sample withdrawal, Online GMP Monitoring, To Support of Product and Process Validation

Diploma/D. Pharmacy/B. Pharmacy; Operating Granulation, Compression, Coating, Capsule Filling, Blister & Bottle Packing Equipment. Supervising Granulation & Packing Lines. Experience in Autoclave, Filling, Vial Washing, Packing Areas

M.Sc, M.Tech, B.Pharm having 2 to 6 years of experience of Biotech and Chemical Analysis e.g., Electrophoresis, Bioassay, HPLC & GC.

To Perform analytical activity of Development, Scale-up support, Method validation, Method transfer, Release, Stability, Drug product characterization, E&L study, In-Vitro study, routine analysis of inhalation dosage forms. M.Pharm, MSc

Centre of Excellence on Phytopharmaceuticals and Herbal Products; PhD in Chemistry organic/ natural products/medicinal/ pharmaceutical chemistry. M.S./M.Pharm. degree in Pharmacology and Toxicology. Postgraduate degree M.S./ M.Pharm. /M.Sc. in chemistry/medicinal chemistry/ natural products/pharmaceutical chemistry/ herbal technology. Experience in natural product extraction, isolation and purification, working in herbal industries, experience in large scale extraction in GMP and GLP facilities. Candidates having knowledge in preparation of SoP and regulatory norms in drug discovery specially for development of cGMP facility / NABL, will be given preference.