• 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
Topical Formulation, Semi Solid Manufacturing, Cream Ointment Gel Production, QMS, SAP, In Process Checks, Deviation Handling and CAPA, Audit readiness and documentation, Production Planning and Scheduling, Cross functional collaboration, Team Supervision, Process Optimization.
B.Pharma OR D. Pharma with minimum of 6 years of experience in procurement of drugs and other pharmaceutical, medical products, relevant experience in public sector, private sector, any reputed organization OR M. Pharma with minimum of 2 years of experience in procurement of drugs and other pharmaceutical, medical products, relevant experience.
Candidate should have strong understanding of OSD manufacturing processes and knowledge of cGMP and relevant regulatory requirements. Monitoring critical process parameters during manufacturing. Candidate should have sound knowledge of QMS - Incidents, Change control, Deviations etc. Should be able to handle the team of 8-10 persons
Railway Recruitment Board (RRB) notified regarding tentative exam schedule For Cen 04/2024 Paramedical Post. Amongst it, there were 246 posts for pharmacists and candidates applied from 17th August 2024 to 16th September 2024. Those who applied earlier can appear for Computer Based Test.
5th Pay Level in 7th CPC, Initial pay (Rs.) 29200 for Pharmacist (Entry Grade) Post
For the last six decades Central Government Health Scheme is providing comprehensive medical care to the Central Government employees and pensioners enrolled under the scheme. In fact CGHS caters to the healthcare needs of eligible beneficiaries covering all four pillars of democratic set up in India namely Legislature, Judiciary, Executive and Press.
Day-to-day production activities, Machine operation, GMP Compliance. Exposure to Topical products like; Cream, Lotion, Gel Manufacturing and packing and its documentation. Good Communication, Presentation and Man Management skills.
Looking for clinical Database Developer experience in eCRF build and edit checks build in Veeva studio; Create eCRF specifications, design, develop and unit test and functionally validate clinical trial setup process. Providing support for the mapping and transformation of clinical data to CDISC SDTM standards. Work independently and accountable for study Data Management deliverables; Coordinate with Biostatistician, Clinical, Medical and local study team as applicable