Jessica Boyd

Background

About Jessica Boyd

Highly motivated, self-starter who is adept at working independently with minimal supervision, as well as effectively contributing and collaborating as a team member.* Efficient at independently managing multiple projects to meet divisional timelines utilizing strong organizational and multi-tasking skills to ensure work is completed in compliance with company guidelines and standards.* Customer focused communicator with ability to lead cross-functional teams and negotiate project issues without compromising rapport and professional relationships.* Eight years of experience working in a cGMP related industry combined with strong knowledge of FDA, ICH, and USP guidelines.* Six years of experience executing and implementing test method validations for new and existing diagnostic products.* Proficient at writing quality documents and using various computer software applications. Specialties:* FDA, ICH, and USP knowlege * Strong cGMP work environment experience * Test method development/validation * Writing/implementing quality documents * DNA restriction mapping * SDS-PAGE & Western Blot * EIA assays * Fermentation * USP testing (microbiology)* Manufacturing/testing of diagnostic products