Full Job Description
Writer drafts procedures, protocols, and investigation (CAPA) documents in support of day-to-day QC laboratory operations.
Writer will ensure the document is progressed through its lifecycle either manually or in the appropriate system of record.
Writer will oversee daily updates of document trackers/ spreadsheets to ensure target dates are met.
Translates requirements into appropriate content that complies with FDA and other governmental agency regulations.
Interacts with project team personnel (including Engineering, Medical, Marketing, and Regulatory) to obtain technical information needed to create content
Ensures technical writing outputs adhere to departmental standards and practices. Coordinates and obtains necessary approvals for release of documentation.
Job Type: Contract
Salary: $25.00 - $33.00 per hour
Schedule:
8 hour shift
Day shift
Monday to Friday
Experience:
Technical writing: 4 years (Required)
Pharmaceutical background: 4 years (Required)
Adobe framemaker: 4 years (Required)