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
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
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: Prepare CTD, ACTD Dossiers and file regulatory submissions Perform assessments of new or revised products Manage complaint documentation (including investigation and closure) Respond to inquiries from regulatory bodies. Should be technically well versed with requirements for
Job Title Senior Regulatory Affairs Specialist Job Description Job title: Senior Regulatory affairs specialist Reports to: Regulatory Affairs Lead Location: Bangalore Position Summary: The Regulatory Affairs Specialist supports and implements product regulatory plans, provides guidance on global regulatory strategy and product registrations, participates in and advise
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
Job Title Sr. Manager Regulatory Affair Job Description Job Posting Description Position Summary: You will be part of the Regulatory Affairs team for AV business within Clinical informatics. Leading teams in regulatory strategy development in a dynamic business environment that ensure
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
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
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
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,
Regulatory Affairs Specialist Job Description: Designation: Regulatory Affairs Specialist Experience Range: 3 to 5 yrs Job Location: Bangalore (Hybrid) About Anumana: Unlocking the language of the heart. Anumana is a new AI-driven company from nference and Mayo Clinic, delivering ECG