B.Pharmacy from recognized institute, Approved Diploma in Pharmacy recognized by the pharmacy council of India and registered as pharmacist under the Pharmacy act 1948.
Organize and dispense the drugs, medicines to the employees, pensioners. Maintain digital records of all the dispensary items, drugs. Any other work as assigned by the Competent Authority from time to time. experience as an apprentice trainee from a recognized Institution in Pharmacy trade
Lead optimization and in vivo proof-of-concept studies of novel alpha-ketoamide based protein aggregation modulators for Alzheimers disease. First class M.Pharm / M. S. Pharm. / M.Tech Pharm/ M.Tech in Medicinal Chemistry/Pharmaceutical Chemistry with GATE/ GPAT/ CSIR UGC-NET including lectureship or equivalent examination
Applications are invited from suitable candidates for the post of Research Associate to work on various NDDS level drug delivery systems for clinical applications in the IPCA foundation industrial project sanctioned to undersigned. M. Pharm, M.S. Pharmaceutics , Industrial Pharmacy or any other equivalent discipline.
B.Pharm with degree, diploma in Clinical Research Methodology. The candidate with a minimum 1 year experience in conducting clinical trial will be given preference. The candidate having experience in insurance sector will be preferred. TMC is an autonomous body funded, controlled by the Department of Atomic Energy, Government of India.
Exposure to OSD Manufacturing operations like Granulation, Compression, Pellet coaling, Capsule filling, Primary Packing & Secondary Packing. Expertise in e-BPR and e-log will he added advantage. Experience of HPLC, UV spectrophotometer and Dissolution Tester operation. Experience of Analytical Method Validation/Transfer. Experience of GC, ICPMS and/or LCMS operation.
Redaction of clinical trial documents in accordance with evolving global regulations. Develop training and drive change management for novel processes related to the EU Clinical Trial Regulation and other regulations. Manage and Coordinate redaction of clinical documents in accordance with EMA Policy 0070, Health Canada Public Release of Clinical Information, PRCI, EU Clinical Trial Regulation, and other global regulations.
B.pharmacy and approved diploma in pharmacy. ECHS invites application to engage featuring medical, paramedical and non-medical staff on contractual bases in ECHS polyclinics ie Amritsar, Tarn Taran and Ajnala for a period of one year
Support Analytical project leader for setting analytical development strategy. Support in data interpretation, results compilations and sharing the information with critical observations and proposals to project team.