Medical Regulatory Executive

Job description: Novacare Healthcare Solutions Pvt Ltd is a leading pharmaceutical distribution company dedicated to providing high-quality products and services to the healthcare industry. Job Summary: We are seeking a Medical Billing Executive to manage and process medical billing transactions, ensuring accuracy, compliance, and timely reimbursement. Key...

Job Description: Medical Content WriterLocation: Jayanagar 3rd Block, Bangalore, IndiaExperience: 3 to 6 YearsBudget: 4 to 6 Lakh INR per annum About Us: We are a leading healthcare organization dedicated to providing high-quality medical content to healthcare professionals and patients alike. Our mission is to make medical knowledge accessible and...

ce: 5-8 yrs **Qualifications**: You have successfully completed a course of studies in a technical or clinical field, preferably in engineering, medicine, medical engineering or (medical) informatics You can offer extensive professional experience in regulatory affairs for Software as Medical Device, SaaS, and/or cloud deployments You have a sound knowledge...

Develop and review content for various regulatory documents; ensure quality as per set regulatory standards and compliance requirement. - Good understanding of global regulatory dossier formats and ACTD/CTD/NeeS/paper dossier format. SKILLS: - Good communication skills (Written and Oral) - MS Office (Excel and Power point) PRINCIPAL RESPONSIBILITIES &...

**Date**:8 Jul 2025 **Location**:Bangalore, KA, IN - Job Description- - Must Have- Job Summary: The Scientific and Medical content teams work on different projects across the product life-cycle from regulatory, safety, medical affairs and commercial solutions for our clients. The team leverages the clinical and scientific knowledge and applies to various...

Company DescriptionSilmed Scientific is a global leader in regulatory affairs, specializing in delivering comprehensive end-to-end regulatory solutions for pharmaceuticals, medical devices, and biosimilars. With expertise in regulatory strategy and successful drug development, the company supports approvals across global markets including Europe, the US,...

ResponsibilitiesLead preparation of Compliance Data Reports (CDRs) and Test Report Forms (TRFs) to demonstrate compliance with IEC 62304, IEC , IEC , ISO , ISO 20417, eIFU Regulation (EU-2021/2226), EU MDR [2017/745], UKCA, Canadian (SOR/98-282), and Australian (TGR) medical device regulations.​Analyze historical Request for Change (RfS) and design change...

**About the job**: **Job Title**:Medical Writer** Company: MS Clinical Research Pvt Ltd Location: Indiranagar, Bangalore Experience: 2-4 years **About MS Clinical**: MS Clinical is a dynamic and innovative company dedicated to advancing medical research and improving patient outcomes. We specialize in conducting clinical trials and providing...

Job Description Responsibilities - Lead preparation of Compliance Data Reports (CDRs) and Test Report Forms (TRFs) to demonstrate compliance with IEC 62304, IEC 82304-1, IEC 62366-1, ISO 15223-1, ISO 20417, eIFU Regulation (EU-2021/2226), EU MDR [2017/745], UKCA, Canadian (SOR/98-282), and Australian (TGR) medical device regulations. - Analyze historical...

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our 35,000 employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our...