Online applications are invited from Indian and International candidates for admission to the Ph.D. programs through Research Eligibility Test under different departments in the Faculties of Science, Literature, Social Science, Music and Fine Arts, Commerce, Law, Management and Information Science of Tripura University for the academic session 2024-25.

M. Pharm with 10 years of experience in handling ADME assays and HPLC and LCMS, MS Or Fresh Ph.D. in similar disciplines

Handling end-to-end project management activities for new product launches for all Regulated and semi regulated markets for first launch. Handling Life cycle management and CMO projects.

To perform line clearance activity before starting of different operations like dispensing, manufacturing, filling, inspection, sealing, labeling & packing.

Person should know QMS, IPQA, validation, Qualification, Cleaning Validation, Risk Assessment, CSV, regulatory requirements, Market Complain, Vendor Qualification, OOS, OOT, Product Recall, Investigation, Regulatory requirement, audit & response.

M.Sc, M.Pharma, B.Pharma. Working in QC analyzing, Stability. In process. FP. RM sample. Handling instruments like HPLC. GC. FTIR. UV, DR. SSA. etc. versatile In handling SAP. documentation like preparing STPs and review of analytical hard copies and electronic data.

Purchase requisition creation, Purchase order creation in SAP-MM, Run RFQ with vendor suggested by sites, receive and compare quotes.

Diploma in pharmacy from a recognized institute. Registered under Jharkhand state pharmacy council computer proficiency MS office and Internet

Masters degree in Botany, Medicinal Plants, Dravyaguna, Pharmacognosy, Forestry, Agronomy, Agri-business, Agri- engineering, Horticulture. National Medicinal Plants Board, Ministry of AYUSH proposes to prepare a panel for engagement of Program Manager, Domain Expert, Project Management Consultants and Junior Consultant

Graduation in science; B.Pharm., Life science, B.Sc., Bio-Tech, zoology, botany etc., with PG diploma in clinical research is desirable.; Working in collaboration with the PI and with a multidisciplinary research team to ensure that rigorous clinical research standards are maintained. Pre-screening and helping in enrolling subjects, participants in studies and managing their participation according to ethical, regulatory, Institution SOP and protocol-specific requirements.

M.S. Pharma, M.Tech, M.Sc in Biotechnology with first- class. OR M.Sc in Biochemistry, Microbiology with first- class in the DBT-NER Advance Level Institutional Biotech Hub sponsored project through walk-in interview.

The role and responsibilities will align with that of a clinical pharmacist. The candidate is also expected to supervise the project activities pertaining to antimicrobial stewardship.

Ensure the core scientific principles of the study are adhered to, including accurate data collection, participant adherence to protocols, and minimizing missing data and loss to follow-up.

First class postgraduate degree including the integrated PG degree with Ph.D in Biotechnology, Biochemistry, Molecular Biology or related areas from reputed University, Institute. The project involves the development of biocompatible nanomaterial-based delivery of siRNA and ASOs based therapeutics for Facioscapulohumeral Muscular Dystrophy.

The candidate should have or be pursuing a Masters degree M.Pharm. in Pharmacology or Masters degree in Biotechnology. Candidates having experience in Animal cell culture techniques and, or laboratory animal experimentation along with Molecular biology, and Immunological techniqueswill be preferred. 

M.Sc. in Botany, Biochemistry, Biotechnology, Life Sciences or a related field; NET, GATE or equivalent; Molecular characterization of a legume lectin-like protein from Arabidopsis thalicina to uncover its role in abiotic stress mitigation and related signaling

Granulation, Coating, Compression, Bottle Packing Machine Exposure, RMG, FBE, FETTE, Autocoaters /Bottle Packing line with track and trace system. To supervise and monitor day to day activities of processing and holding of drug product as per define and approved procedures for stability batches and commercial batches.

Looking to hire Head Of Regulatory Affairs - an aggressive, dynamic Regulatory Affairs Professional. Who would assume the Regulatory strategic, filing and post approval life cycle management and Quality, Technical and regulatory compliance responsibilities as per EU, UK, USA, and PIC, s requirements.