Contract: SOP Technical Writer


Position Description

Bachelor’s Degree in the Life Sciences or Engineering field, or similar with 2-5 years of GMP experience with expertise in authoring fundamental Quality System SOPs for an FDA regulated company.

Key Skills:
• Experience drafting new SOPs and editing existing SOPs to align with current practices
• Excellent writing and oral communication skills
• Ability to exercise judgment within defined procedures and practices to determine appropriate action with minimal supervision
• Maintain standardized language and documentation that allow for consistent execution of documents
• Advanced MS office skills including Word
• Well organized and detail oriented with the ability to handle multiple tasks

Type: Contractor