Center for Advance Research on Medical Devices Development, Characterization and Validation. A clinical trials approach Aims to provide a comprehensive platform for the end-to-end development, testing, and validation of medical devices.
Center for Advance Research on Medical Devices Development, Characterization and Validation A clinical trials approach: Aims to provide a comprehensive platform for the end-to-end development, testing, and validation of medical devices.
Serve as a Subject Matter Expert on all In-Take Team complaint processes and scenarios and assists QAS employees to ensure compliance with Quality Assurance Services Standard Operating Procedures and Work Instructions
Review, assess and process Safety data and information, across service lines, received from various sources and distribute reports/data onwards to both internal and external third parties following applicable regulations SOPs and internal guidelines under guidance and support of senior operation team members.
Preparation of quality system related, Instrument operation related SOPs, Specification, STPs, GTPs, raw data sheet, certificate of analysis. Preparation, review, execution of method transfer and method validation protocols and reports etc.
Support implementation of Marketing-led initiatives including supporting coordination with partner agencies to deliver appropriate campaign content, logistic support for cycle and kick-off meetings, patient-focused solutions and multi-channel and digital campaigns.
CSIR-Central Institute of Medicinal and Aromatic Plants (CSIR-CIMAP) is a premier multidisciplinary research institute of Council of Scientific and Industrial Research (CSIR), India with its major focus on exploiting the potential of medicinal and aromatic plants (MAPs) by cultivation, bioprospection, chemical characterization, extraction, and formulation of bioactive phytomolecules.
Baxter provides a broad portfolio of essential renal and hospital products, including home, acute and in-centre dialysis; sterile IV solutions; infusion systems and devices; parenteral nutrition; surgery products and anesthetics; and pharmacy automation, software and services. The company’s global footprint and the critical nature of its products and services play a key role in expanding access to healthcare in emerging and developed countries.
Post : Principal Specialist, Regulatory Affairs (Hybrid)
GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. Getting ahead means preventing disease as well as treating it, and we aim to impact the health of 2.5 billion people around the world in the next 10 years.