Medical Regulatory Executive

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...

**Role**: - Medical Sales Representative (Field Sales) **Location**: - Jayanagar, Bangalore. **Experience**: - 1-5 Years Designation - Business Development Executive **Preferred Industry**: - Medical/Healthcare/hospitals/Pharma.

The Medical Records Executive is responsible for the management, organization, and maintenance of patient medical records in compliance with hospital policies and regulatory standards. The role ensures the timely and accurate filing, retrieval, and safeguarding of medical documentation. **Key Responsibilities**: - Maintain and update patient medical...

Medical Device Regulatory Compliance SpecialistThe role of the Medical Device Regulatory Compliance Specialist is to ensure that medical devices are compliant with regulatory requirements. This includes ensuring compliance with ISO 13485, MDD, MDR, GMP, GDP, and QMS standards.Key Responsibilities:Coordinate with regulatory authorities for obtaining required...

Global Regulatory Medical Writer RoleJob Description:The Global Regulatory Medical Writer plays a critical role in the development and submission of clinical regulatory documents. This includes writing, editing, and formatting complex documents such as study reports, protocols, and investigator’s brochures.Responsibilities include:Writing and editing...

Provide responses to regulatory agencies regarding product information or issues. - Train RA Assistant and staffs in regulatory policies or procedures. Coordinate internal discoveries and depositions with legal department staff. - Develop and maintain standard operating procedures or local working practices. - Establish regulatory priorities or budgets 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...

**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...

This role plays a pivotal part in bringing medical devices to market while ensuring ongoing compliance. Key responsibilities include participating on cross-functional teams, developing global regulatory strategies, authoring regulatory submissions, and interacting with regulatory agencies.The ideal candidate will have expertise in product development...

Opportunity to lead QA RA for medical implants greenfield projectSet up and maintain the Quality Management System in ISO 13485About Our ClientGlobal medical devices client in the space of orthopedic implantsJob DescriptionRegulatory Affairs:Lead interactions with Indian health authorities (CDSCO) for the registration and continued compliance of our implants...