Senior Regulatory Content Specialist

2 days ago

Las Piñas, National Capital Region, Philippines beBeeTechnicalEditor Full time ₱900,000 - ₱1,330,000
Job Description

The role of a Technical Editor II is to oversee the editing process, ensuring that documents meet client and project specifications.

  • Edit documents according to templates, style guides, and other guidance documents while considering business goals, project deliverables, timelines, and budgets.
  • Communicate directly with clients to establish clear expectations for project deliverables in relation to business goals and provide leadership within internal review teams.
Main Responsibilities

This position requires strong proficiency in quality control review, including verification of document against source, internal consistency, and grammar based on understanding of grammar rules.

  • Perform formatting techniques consistent with company guidelines, including template utilization, style application, table insertion, figure creation, overall document appearance, and function.
  • Publish documents to regulatory health standards and learn requirements for submission-ready documents and the submission structure.
  • Lead document quality-related projects, coordinate with team members, manage timelines, communicate client feedback, and propose performance improvement ideas.
  • Demonstrate clear and effective written and verbal communication, remain compliant with applicable standard operating procedures, work instructions, and technical editor best practices.
Requirements

To be successful in this role, you will need:

  • A Bachelor's degree in English, journalism, scientific discipline, or related field with an interest in regulatory writing.
  • Editor in the Life Sciences certification is desired but not required.
  • Strong computer skills, including Microsoft Office Suite proficiency in editing tools, table creation, and figure insertion.
  • At least 2 years of prior related experience; highly skilled, talented, and motivated candidates will be considered.
  • Background in pharmaceuticals and/or science and technical industries is preferred.
  • Understanding of GXP, ICH E3, electronic Common Technical Document (eCTD), AMA style guidance, and version control, and MS Word template.
  • Proven success in a team-based environment.

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