Senior Regulatory Document Writer

Job Title:Regulatory Medical WriterJob Description:We are seeking an experienced Regulatory Medical Writer to join our team. As a key member of our medical writing department, you will be responsible for drafting and managing clinical documents such as Protocols, Investigators Brochures (IB), Informed Consent Documents (ICD), and other regulatory submission...

Job Title: Technical Writer – ImmunodiagnosticsLocation: Banglore-HybridRole Overview:We are seeking a skilled Technical Writer to develop and maintain clear, accurate, and compliant documentation for immunodiagnostic products, including IFUs, user manuals, product labels, and digital learning aids.Key Responsibilities:- Create and edit high-quality...

We are a technology-led healthcare solutions provider.We are driven by our purpose to enable healthcare organizations be future ready.We offer accelerated, global growth opportunities for talent that's bold, industrious and nimble.With Indegene, you gain a unique career experience that celebrates entrepreneurship, and is guided by passion, innovation,...

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...

Job Role SummaryAbout Senior Technical Writer PositionThe successful candidate will be a skilled and experienced Technical Writer who can create high-quality documentation for our products.Key Responsibilities:Develop user manuals, guides, and knowledge base articles that are clear, concise, and easy to understand.Create technical documentation, such as...

Key Medical Content Writer RoleThe organization is seeking a highly experienced Key Medical Content Writer to fill a key role in our content creation team. The ideal candidate will have 4-8 years of experience in writing clinical and regulatory documents, with a focus on supporting global filings.Principal Responsibilities:Writing and editing high-quality...

Job Title: Technical Writer – ImmunodiagnosticsLocation: Banglore-HybridRole Overview:We are seeking a skilled Technical Writer to develop and maintain clear, accurate, and compliant documentation for immunodiagnostic products, including IFUs, user manuals, product labels, and digital learning aids.Key Responsibilities:Create and edit high-quality...

Job Title: Technical Writer – Immunodiagnostics Location: Banglore-Hybrid Role Overview: We are seeking a skilled Technical Writer to develop and maintain clear, accurate, and compliant documentation for immunodiagnostic products, including IFUs, user manuals, product labels, and digital learning aids. Key Responsibilities: Create and edit...

As a Technical Documentation Writer, you will play a critical role in ensuring our customers and internal teams have access to clear, concise, and accurate documentation. You will work closely with product managers, developers, and other stakeholders to understand our products and translate complex technical information into easy-to-understand guides,...

Regulatory Affairs Professional Job DescriptionOur team seeks a skilled Regulatory Affairs Associate Senior to lead the publishing and dispatch of regulatory submissions for Devices & Drugs Submissions. Key responsibilities include:Managing and leading regulatory publishing operations globally.Ensuring submissions meet eCTD requirements and other regional...