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 Device
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.
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
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 of technical
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
Company Description Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable
Job title: Manager- Regulatory Affairs Grade: L 2.2 Hiring Manager: Sanjeev Kumar Location - Mumbai 40% Remote working and 20 % of travel expected Job type: Permanent About the job Our Team: Brief introduction of the department, team,
Summary of Position: Product Regulatory Affairs (Life Sciences & Agriculture) work includes: •Directing submission development of product registration, progress reports, supplements, amendments, and/or periodic experience reports •Providing strategic product direction to teams on interaction and negotiating evidence with
A Day in the Life Manage, plan and execute the preparation, review and submission of dossiers for product registrations, import licenses and other approvals from regulatory agencies (registrations and renewals) thereby supporting the business units and supply
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
About Apotex Inc. Apotex Inc. is a Canadian-based global health company that produces high-quality, affordable medicines for patients around the world. Apotex employs almost 7,200 people worldwide in manufacturing, R&D, and commercial operations. Apotex medicines are
About Apotex Inc. Apotex Inc. is a Canadian-based global health company that produces high-quality, affordable medicines for patients around the world. Apotex employs almost 7,200 people worldwide in manufacturing, R&D, and commercial operations. Apotex medicines are
Company Description GPC Medical Ltd. is an Indian hospital and medical supplies company with decades of experience supplying high-quality medical equipment and orthopedic implants/instruments all over the globe. The company is ISO 13485 Certified, WHO-GMP Compliant,
Job Title: Regulatory Affairs Lead (Manager/Senior Manager) Company: BDR Lifesciences Location: Vadodara, India About BDR Lifesciences: BDR Lifesciences is a leading pharmaceutical company dedicated to improving healthcare through the development, manufacturing, and marketing of high-quality active pharmaceutical ingredients
• Experience to prepare and review the documentation required for the ISO 9001:2015, EN ISO 13485, Quality management System, MDR for Medical Devices. • Knowledge and preparing documents such as Quality Manual, Site Master File, SOP’s,
Organisation : USV, a top -15 pharmaceutical company in India, excels in the diabetes and cardio sectors. With a presence in over 65 countries, our dynamic team of over 7,000 spans generations. Our commitment to brand
Works within a team environment or individually based on the project needs Provides guidance to project team members Works within broad project guidelines and facilitates issue and conflict resolutions Prioritizes own work load and may prioritize
We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations to be future ready. We offer accelerated, global growth opportunities for talent that’s bold, industrious and nimble. With Indegene,
Role Description: Preparing the NDA submission for Emerging Markets, communicating with regulatory agencies, and managing the regulatory review process. Ensuring that the drug is approved for marketing in a timely manner and that it meets the regulatory requirements for