To work on project entitled Identification and validation of new potential protein biomarker panel for head and neck squamous cell carcinoma using translational proteomics. 1st class post graduate degree including the integrated Master degree in life sciences.
Operational Excellence - Build on technical expertise, expanding it in complementary directions. Use technical expertise and creativity to proactively identify potential problems and address them using appropriate resources in discussion with team leads.
Degree, Diploma in Pharmacy form recognized University. One Year experience in Managing Drug Store in reputed Hospital, Health Centre recognized by Govt. Candidate Should be well Conversant with Various Computer Programming include Excel, MS. Word, PPT and simple Statistical Package.
Applications are invited for the post of Project, Executive Assistant on the project titled Sustainable Monomer Synthesis from Polymeric Waste sponsored by JSW Paints Pvt. Ltd. under the supervision of Dr. D V. Pinjari, Department of Polymer & Surface Engineering.
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.
TCS combines tech expertise and business intelligence to catalyze change and deliver results. Our mission is to help customers achieve their business objectives by providing innovative, best-in-class consulting, IT solutions and services and to make it a joy for all stakeholders to work with us. Clinical Data, Regulatory, Clinical Operations, Pharmacovigilance; Should be open to work In shifts
Hands-on experience with HPLC, GC, UV-Visible Spectroscopy and Dissolution tester. Proficient in Empower-3 software.
Strong analytical and problem- solving skills.
• Clinical Research (PGDCR/EDCR) • Pharmacovigilance (PGDPV/EDPV) • Pharmaceutical Regulatory Affairs (PGDPRA/EDPRA) • Pharmaceutical Quality Assurance and Quality Control (PGDPQAQC/EDPQAQC) • Big Data Analytics (PGDBDA/EDBDA) • Medical Device Management (PGDMDM/EDMDM) • Pharmaceutical Sciences (PGDPS/EDPS) • Pharmaceutical Business Analytics (PGDPBA/EDPBA) • Medical Coding (PGDMC/EDMC) • Good Manufacturing Practices (PGDGMP/EDGMP) • Food Science and Technology (PGDFST/EDFST) • Nanotechnology (PGDNT/EDNT) • Clinical Psychology (PGDCP/EDCP) • Public Health and Hospital Management (PGDPHHM/EDPHHM) • Intellectual Property Rights (PGDIPR/EDIPR) • Pharmaceutical Regulatory Affairs (PGDPRA/EDPRA) • Environmental Social & Governance (PGDESG/EDESG) • Environment Health and Safety (PGDEHS/EDEHS) • Environment Regulatory Affairs (PGDERA/EDERA) • Environmental Studies and Resources Management (PGDESRM/EDESRM) • Herbal Formulations (PGDHF/EDHF) • Cognitive Behavioural Therapy (CBT) • Neuropsychology (PGDNP/EDNP) • Integrative Medicine (PGDIM/EDIM) • Maternal and Child Health (PGDMHC/EDMHC) • Yoga Therapies (PGDYT/EDYT) • Ayurveda Practices (PGDAP/EDAP/DAP) • Public Health and Hospital Management (PGDPHHM/EDPHHM)
• Pharmaceutical Management (PGDPM/EDPM) • Pharmaceutical API Manufacturing (PGDPAM/EDPAM) • Pharmaceutical Formulation (PGDPF/EDPF) • Pharmaceutical Chemistry (PGDPC/EDPC) • Pharmaceutical Process Engineering (PGDPPE/EDPPE) • Herbal Drug Technology (PGDHDT/EDHDT) • Herbal Medicine (PGDHM/EDHM) • Bioinformatics (PGDBI/EDBI) • Pharmaceutical Packaging (PGDPP/EDPP) • Pharmaceutical Production (PGDPP/EDPP) • Computer Aided Drug Design (PGDCADD/EDCADD) • Computer System Validation (PGDCSV/EDCSV) • Regulatory Affairs (Medical Device as Major) (PGDRAMDM/EDRAMDM) • Biomedical Technology (PGDBT/EDBT) • Nanomedicine • Ayurvedic Cosmetology (PGDAC/EDAC) • Cosmetic Technology (PGDCT/EDCT) • Herbal Cosmetics (PGDHC/EDHC) • Dermacare Formulations (PGDDF/EDDF) • Clinical Nutrition (PGDCN/EDCN) • Sports and Fitness Nutrition (PGDSFN/EDSFN) • Nutrition and Dietetics (PGDND/EDND) • Obesity and Weight Management (PGDOWM/EDOWM) • Clinical Diabetology (PGDCD/EDCD) • Public Health Nutrition (PGDPHN/EDPHN) • Medical Nutrition Therapy (PGDMNT/EDMNT) • Pediatric Nutrition (PGDPN/EDPN)
Certificate Programmes:
• GMP for Pharmaceutical & Manufacturing Processes • Pharmaceutical GMP Auditor • Medical Device Quality Auditor • Drug Regulatory Affairs Professional • Good Laboratory Practice Professional (CGLPP) • Certified Sports Nutritionist • Certified Fitness Nutrition Specialist • Certified Diabetes Educator • FSMS Lead Auditor (5 Days Training) • FSSC 22000 Lead v6 Auditor (5 Days Training) • HACCP Level 4 Auditor (5 Days Training) • Food Regulatory Affairs Professional (5 Days) • Food Quality Manager (5 Days) • Food Quality Technician (5 Days) • Laboratory Management Systems (ISO/IEC 17025:2017) Lead Auditor Training (5 Days) • Certificate in Occupational Health and Safety Management Systems (OHSM) • Corporate Social Responsibility Compliance (CSRC) • Environmental Social & Governance (ESG) • Healthcare Waste Management
• Food Safety Management Systems (FSMS) (5 Days Training) • HACCP (3 Days Training) • BRC Global Standards for Food Safety and Quality (5 Days Training) • Food Packaging (5 Days) • Food Supply Chain Management (5 Days) • Good Manufacturing Practices (5 Days) • Food Sensory Analysis (5 Days) • Dairy Science and Technology (5 Days) • Cold Chain Management (5 Days) • Entrepreneurship Development in Food Industries (5 Days) (e.g., Bakery, Beverage, Milk Industry) • Food GMP Professional (5 Days) • Food Quality Auditor (5 Days) • FSMS Internal Auditor (5 Days Training) • Business Responsibility and Sustainability Report (BRSR) • Environmental Management Systems (ISO 14001:2015) Lead Auditor
✓ Programme duration: Programme duration: 12 months for Post Graduate Diploma, 6 months for Executive Diploma and 3 months for Professional Certification programmes.
✓ Contact for Prospectus and last date on: 18001031071 or info@igmpi.ac.in
Post Graduation in Science M.Pharm, Life Sciences, Biotech, Zoology, Botany, etc. With PG Diploma in Clinical Research is mandatory. Candidates should have at least one-year experience as Clinical Trial / Research Coordinator is mandatory.
Tevas Global Regulatory Affairs Policy and Intelligence team is at the forefront of regulatory policy and intelligence, transforming complex regulatory landscape updates into actionable insights to inform regulatory strategy and cross-functional strategic decision-making.