Verified Job
Work from home
Publishing Officer/ Specialist
Work from home
#766021
Remote / WFH
ProductLife Group
Job Description
The Publishing Officer/ Specialist will support regulatory submission publishing activities for global markets as part Publishing project. The role focuses on the preparation, compilation, and publishing of regulatory submissions in multiple electronic formats, ensuring compliance with regional regulatory authority requirements and internal quality standards.
This position is a replacement role with long-term project visibility (3+ years) and offers the opportunity to work in a global regulatory environment
Key Responsibilities
Perform regulatory publishing activities in eCTD, NeeS, ePaper, and ACTD formats.
Support submissions across EU, US, Canada, Australia, GCC, ASEAN, and other global regions.
Compile, publish, and validate regulatory submissions in line with health authority requirements.
Ensure accuracy, consistency, and technical compliance of published submissions.
Coordinate and plan assigned publishing projects in collaboration with internal stakeholders.
Perform quality checks and address validation findings prior to submission.
Maintain submission documentation and ensure proper version control.
Work effectively within defined timelines while managing multiple submissions.
Required Qualifications
Bachelor’s degree in Life Sciences or a related discipline.
5+ years of experience in Regulatory Affairs / Regulatory Operations with hands-on eCTD publishing exposure.
Experience working on international, EU, and RoW submissions.
Technical Skills
Experience with eCTD and NeeS publishing.
Strong knowledge of electronic document management systems (eDMS).
PDF preparation and editing using Adobe Acrobat Pro.
Hands-on experience with DocuBridge (Preferred
Familiarity with ISI Toolbox / Evermap (bookmarks, hyperlinks, TOC creation).
Basic understanding of Regulatory Affairs processes and submission lifecycle.
Soft Skills & Competencies
Highly organized and methodical approach to work.
Strong attention to detail and quality mindset.
Ability to manage priorities and work under tight timelines.
Adaptable and comfortable working in a global, remote environment.
Clear communication and collaboration skills.
This position is a replacement role with long-term project visibility (3+ years) and offers the opportunity to work in a global regulatory environment
Key Responsibilities
Perform regulatory publishing activities in eCTD, NeeS, ePaper, and ACTD formats.
Support submissions across EU, US, Canada, Australia, GCC, ASEAN, and other global regions.
Compile, publish, and validate regulatory submissions in line with health authority requirements.
Ensure accuracy, consistency, and technical compliance of published submissions.
Coordinate and plan assigned publishing projects in collaboration with internal stakeholders.
Perform quality checks and address validation findings prior to submission.
Maintain submission documentation and ensure proper version control.
Work effectively within defined timelines while managing multiple submissions.
Required Qualifications
Bachelor’s degree in Life Sciences or a related discipline.
5+ years of experience in Regulatory Affairs / Regulatory Operations with hands-on eCTD publishing exposure.
Experience working on international, EU, and RoW submissions.
Technical Skills
Experience with eCTD and NeeS publishing.
Strong knowledge of electronic document management systems (eDMS).
PDF preparation and editing using Adobe Acrobat Pro.
Hands-on experience with DocuBridge (Preferred
Familiarity with ISI Toolbox / Evermap (bookmarks, hyperlinks, TOC creation).
Basic understanding of Regulatory Affairs processes and submission lifecycle.
Soft Skills & Competencies
Highly organized and methodical approach to work.
Strong attention to detail and quality mindset.
Ability to manage priorities and work under tight timelines.
Adaptable and comfortable working in a global, remote environment.
Clear communication and collaboration skills.
