Medical Affairs Manager

Role - Regulatory Affairs - Medical Devices Experience - 1 to 3 Years Location- Madhavaram Chennai Budget - As per the industry Key Responsibilities 1 Regulatory Submissions Prepare and submit regulatory documents to authorities for approval such as new product applications amendments and supplements 2 Compliance Ensure products meet...

Medical Affairs Specialist - India Chennai Trivandrum - Office or Home BasedICON plc is a world-leading healthcare intelligence and clinical research organization Were proud to foster an inclusive environment driving innovation and excellence and we welcome you to join us on our mission to shape the future of clinical developmentOverview Provide support...

Medical Devices SpecialistWe are seeking a highly experienced professional to lead our medical devices team.The ideal candidate will have at least 10 years of professional experience in the medical devices industry, with expertise in quality management, regulatory affairs, and research and development. Essential skills include risk management EN ISO 14971,...

JOB DETAILS 1.Be the medical expert for the therapy area and the medical lead within the brand teaminputting into the strategy for the brand2.Support the Medical Director in carrying out the day to day operational activities of theMedical Department.3.Review and sign-off of promotional and non-promotinal material to ensure compliancewith the Codes of...

Medical Advisor RoleJob OverviewWe are seeking a skilled medical professional to contribute to the development of our medical affairs strategy within the brand team.Act as a medical expert and lead key initiatives, contributing to strategy development and execution.Support operational activities and provide expertise in managing day-to-day operations.Review...

Regulatory Affairs Specialist Job OpportunityThe ideal candidate for this position will have a strong background in regulatory affairs, with a focus on CMC and USFDA submissions.A key responsibility of the role is leading and managing CMC regulatory activities, including preparing and reviewing technical documents such as Module 2 & 3 (CTD format).Key...

Job RoleOverview:This role involves providing medical scientific consultation to internal and external customers with oversight from a Medical Monitor.The primary responsibility is to ensure daily medical management activities are completed in accordance with industry standards.Travel requirements include < 10 domestic and/or international trips, serving as...

Job Title:Senior Scientific Content EditorWe are seeking a highly skilled and experienced Senior Scientific Content Editor to review, edit, and ensure the quality and accuracy of medical and scientific documents. This role involves working closely with medical writers and subject matter experts to produce clear, consistent, and compliant content for...

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 and innovative medicines because Good Health Can't Wait.We started in 1984 with a modest investment, 20...

Medical Device R&D RolesWe are seeking experienced professionals to drive compliance activities and lead successful QMS processes at a medical device facility.The selected candidates will be responsible for various roles including Design Quality, Mechanical Engineering, Electrical & Electronics Engineering, and Software Engineering.Key...