Technical Writer

Contract Length:  1 year with possible extension

 

Job Summary:  Will be working with IT Compliance group which is in charge of investigations for the IT Depts. regarding deviations in the systems they manage. 

 

Responsibilities:

• Write, create, draft, edit, review and maintain documents designed to explain and test laboratory systems.
• Write, modify and or change controlled documents.
• Write, review, and maintain department standard operating procedures.
• Edit, standardize, or make changes to materials prepared by other writers or personnel.
• Coordinate projects and documentation assignments

 

Requirements:

• BS/BA degree required
• 5+ years’ experience with bio pharmaceutical equipment or manufacturing, particularly in Quality Review required
• Good documentation practices (GDP) experience preferred
• FDA regulated environments experience preferred
• Laboratory systems experience preferred
• Nonconformance and deviation management experience preferred