Coordinate scientific input from multiple authors, reviewers, and subject matter experts
Track document components across drafting, review, and approval stages
Ensure consistency in scientific terminology, formatting, and messaging across documents
Review documents for clarity, completeness, and alignment with regulatory or client expectations
Identify gaps, inconsistencies, or unresolved comments and drive resolution
Ensure document outputs meet internal quality standards and external regulatory requirements

🎯 Requirements

M.Sc / M. Pharm with 5-7 years of experience
Scientific or technical discipline (e.g., CCIT/Package Testing preferred, Chemistry, Biology, Life
Experience coordinating technical or scientific documentation
Familiarity with regulated environments (GMP, GxP, clinical research, or equivalent)
Strong written communication skills with attention to detail and consistency
Demonstrated ability to manage multiple deliverables and competing priorities

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