Professional 1 Regulatory Publishing

Looking to jump-start your career? We understand how important the first few years of your career are, which create the foundation of your entire professional journey. At Indegene, we promise you a differentiated career experience. You will not only work at the exciting intersection of healthcare and technology but also will be mentored by some of the most...

Veranex is the only truly comprehensive, global, tech-enabled service provider dedicated to the medical technology industry. Offering expert guidance from concept-through-commercialization, including product design and engineering, preclinical and clinical development, data management, market access, regulatory affairs and quality assurance, Veranex enables...

About the jobKey Responsibilities:Strong understanding of eCTD, and ICH guidelines.Familiarity with Regulatory systems and Publishing tools.Use publishing tools such as: Mono eCTD, Ectd Validator, Adobe Acrobat, MS Excel, SharePoint.Ability to perform end-to-end eCTD submission process, including Document level Publishing and Dossier compilation, and...

Responsibilities: Coordinate end-to-end publishing workflows, from manuscript submission to final production.Collaborate with editorial teams, authors, designers, and vendors to ensure publishing timelines are met.Perform quality checks on content, layouts, and design before release.Assist in preparing content for digital and print distribution, ensuring...

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...

ClinChoice is a global full-service CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative "one-team" culture. We are looking for a dynamic person to join our in-house team as a Regulatory Operations Trainee on a permanent basis. You will work on projects from our varied client base,...

Job Overview:We are seeking a Regulatory Publishing Specialist with expertise in eCTD format submissions and Veeva Vault to join our team.Main Responsibilities:Prepare and manage BLA (Biologics License Application) submissions in eCTD format using Veeva Vault eCTD Publishing.Compile, format, and publish regulatory documents according to global health...

Familiarity with using publishing tools such as: Mono eCTD, Ectd Validator.Perform end-to-end eCTD submission process, including Document level Publishing, dossier compilation, hyperlinking, bookmarking, and validation and quality checking.Health insurance

Key Responsibilities:Strong understanding of eCTD, NeeS, and ICH guidelines. Familiarity with Regulatory systems and Publishing tools. Use publishing tools such as: Lorenz Docubridge, Ectd Validator, ISI Toolbox, Adobe Acrobat, MS Excel, SharePoint. Ability to perform end-to-end eCTD submission process, including Document level Publishing and Dossier...

Key Responsibilities:Strong understanding of eCTD, NeeS, and ICH guidelines.Familiarity with Regulatory systems and Publishing tools.Use publishing tools such as: Lorenz Docubridge, Ectd Validator, ISI Toolbox, Adobe Acrobat, MS Excel, SharePoint.Ability to perform end-to-end eCTD submission process, including Document level Publishing and Dossier...