Job Description

Max BR of *** per hour including MSP fee (2.3%)

Ideal candidate: B.S. 2-3+ YOE, Strong attention to detail. Microsoft Word programs,
GMP and GDP, and Smartsheet experience.


Nice to have: Previous Pharma or biotech experience. Preferably in pharma manufacturing.


Hybrid - 2-3 days onsite per week.


Job Details: Develops, writes, edits, and formats materials such as Standard Operating Procedures, Business Practices, forms, checklists, technical manuals, installation guides, user manuals, and related technical and business process documentation. When creating, updating and enhancing the documentation, adhere to format, content and style guidelines, giving consideration to usability and ensuring accuracy, consistency and quality. Additionally, this position will be required to administer the processing of documents via the established Document Processing Review process. May require communication through a variety of media (e.g., CD, intranet, on-line training, etc.); Skills: ; MS Office expertise; Smart Sheets expertise, previous technical writing experience; regulated environment experience; document version control experience; excellent communication/writing skills

Job Tags

Hourly pay, 2 days per week, 3 days per week,

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