Who we are Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries
Summary Of Position: Regulatory Affairs Analyst is responsible for providing support in ensuring compliance with EU, US, and global medical device regulatory requirements. This position is primarily focused on supporting international registration requirements triggered by the EU Medical
Job Title: Regulatory Manager About Job: The Regulatory Manager is a management role that manages the regulatory activities involved in the India/Srilanka/Nepal/Maldives market. Manage the regulatory compliance and data needs including regulatory quality compliance, regulatory database updates and maintenance, etc. Support the
Department: RA CMC & Device Are you passionate about your work? Do you want to build excellence within processes in the most efficient way? Do you have an innovative mindset to drive change in a future-ready
Department: RA CMC & Device Are you passionate about what you are doing? Do you want to build excellence within processes in the most efficient way? Do you have an innovative mindset to drive change in
Business Overview J&J MedTech India (JJMI) J&J MedTech India (JJMI) is the market leader in the Medical Technology industry in India. It is in the business of caring and providing solutions to doctors, patients, and nurses.
About the Team The GSMA Mobile Money Programme works with mobile money providers to accelerate the availability of digital payment services to the people of developing countries. Through its work, the GSMA has supported the development
Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich
The Regulatory Solutions Consultant position will involve data monitoring, data authoring, content development, maintenance & operations related to regulatory consulting projects. Individuals would get exposure to Clarivate-owned Life sciences databases and external data sources. The team is highly
Who we are Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries
Your Role: Ability to contribute to the dossier content and to support the life cycle management of regulatory Devices and Drug/Device combination activities. Ability to develop, prepare and implement successful regulatory strategies and dossiers. Experience in preparation and
Department: RA CMC & Device Are you passionate about what you are doing? Do you want to build excellence within processes in the most efficient way? Do you have an innovative mindset to drive change in
Regulatory Compliance Ensure product packaging and associated information are updated, timely implemented and maintained in accordance with the current product licenses. Ensure that Marketing Authorizations are updated in line with Company Core Safety Information according to Corporate
Location: Noida,Uttar Pradesh,India About Testbook : Testbook is the fastest-growing & leading EdTech platform established 10 years ago. We focus on Government & Private Job Exams with an eye to capture UPSC, Banking including Regulatory body, SSC,
Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich
Job Description Preparation of applications and submission packages for various biologics/biosimilars regulatory submissions. Authoring master and country specific dossier sections according to CTD module Review of CMC technical documents required for submissions and ensure compliance with regulations
About Testbook : Testbook is the fastest-growing & leading EdTech platform established 10 years ago. We focus on Government & Private Job Exams with an eye to capture UPSC, Banking including Regulatory body, SSC, Railways, Teaching and
Department: Research & Development Do you want to play a key role in accelerating the development of our patient-focused products? Are you passionate about regulatory science and executing on regulatory strategies to bring innovative medicines to patients? If
We are hiring for Regulatory Affairs Analyst IVD Expert Your Role: The Regulatory Affairs Analyst IVD Expert supports assigned regulatory tasks related to health authority notifications, submissions, and registrations regarding renewals and new products. Independently assemble and support maintenance
Job Responsibilities: Preparation, review & submission of Post approval changes supplements. Responsible for review of OOS, OOT, Change control, deviation As per Regulatory guidelines. Monitoring of Post approval commitments for commercial batches. Preparation, review & submission of