Description:Note:Job Details:Day to Day Responsibilities:
Develops, writes, edits, and formats materials such as Standard Operating Procedures, Business Practices, forms, checklists, guide, 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 ; previous technical writing experience ; regulated environment experience ; document version control experience ; excellent communication/writing skills.
Basic Qualifications
Doctorate degree OR Master degree and 3 years of experience OR Bachelor degree and 5 years of experience OR Associate degree and 10 years of experience OR High school diploma / GED and 12 years of experience.
Top 3 Must Have Skill Sets:
Create, revise, and approve documents in CDOC Veeva
Coordinate and facilitate meetings
Engage multiple people or group of people to get the inputs
Looking for someone who has pharma industry background with experience writing SOPs.
Pay Rate between $40 - $44/Hr on W2 based on experience."This posting is for Contingent Worker, not an FTE"