Location: Woodcliff Lake, NJ
Technical procedural document writer who works with cross-functional/cross-regional teams to draft, revise, and finalize procedural documents and associated documents (Forms and Templates, and training materials if required) to a high quality standard, ensuring that timelines and customer needs are met. Ensure documents are prepared, formatted, and proof-read, including grammatical and technical accuracy as needed, in a timely manner and in compliance with client procedural document writing standards. Perform independent quality control of procedural documents as necessary. Create Process Maps as needed using MS Visio.
Manage the collation, review, and adjudication of comments on procedural document through effective communication with the Process Owners and SMEs. Document and track procedural document development, review, and approval using available departmental tools and electronic systems.
Bachelor's degree in a relevant scientific degree is required
A minimum of 2-3 years of pharma experience is required.
Experience working in a matrix environment across functions
Knowledge of the drug development process preferred
Proven excellent technical writing and word processing skills
Experience using MS Visio would be advantageous
Proven experience in developing, maintaining and using templates and working in an electronic document management system
Excellent communication skills both oral and written at all levels