Having Injectable Experience of Shop floor ac-tivities like vial washing, compounding, filtration, filling and Sealing, Autoclave, Garment Washing machine, Lyophilizes
Must be from Formulation Industry. Undertake method development, troubleshooting and method validation to GMP and ICH. Investigation of non- conforming samples, CAPAs, data evaluation and reporting.
Research experience in Drosophila genetics and epigenetics will be preferred. Masters degree in Natural or Pharmaceutical sciences and Three years of experience in Research and Development in industrial and academic institutions or Science and Technology organizations and scientific activities and services.
M.Sc in Life Sciences, Chemistry from a recognized University or equivalent AND selected through a process described through anyone of the following National Eligibility Tests – CSIR-UGC NET including lectureship Assistant Professorship and GATE.
D.Pharma in aggregate and registered with State Pharmacy Council or Pharmacy Council of India. Individuals qualified in B.Pharma. Applications invited from Domiciles of Districts Of Tamil Nadu, Andhra Pradesh, Telangana, Union Territory Puducherry (Karaikal, Yanam & Puducherry) And Andaman & Nicobar Island (Nicobar, North & Middle Andaman And South Andaman)
Masters, Integrated Masters in Natural or Pharmaceutical Sciences OR Bachelors Degree in Engineering or Technology or Medicine from a recognized University or equivalent AND THREE years of experience in R&D in industrial and academic institutions or ST organizations and scientific activities and services.
Bachelor of Pharmacy B.Pham and Post-graduate in Life Sciences, A Phase 2/3, Multicentre, Open-label trail to evaluate the long-term safety, tolerability, and efficacy of Sibeprenlimab administered subcutaneously in Subjects with Immunoglobulin A Nephropathy
Knowledge of FDA, cGMP, ICH, DMF guidelines for regulatory submissions. Hands on experience in CMC submissions, supplemental applications. Experience working on labels will have added advantage. Excellent written and verbal communication skills; experience in Regulatory Affairs of Finished dosage formulations mainly for USFDA, EU. M Pharmacy / M. Sc. / B Pharm