Experienced Document Control Associate for the pharmaceutical, device and technology industry working in a GLP, GCP, and cGMP environment. Demonstrated project manager for several document management types, with ability to self-prioritize to meet management and customer demands. Responsible for the successful execution of change control activities for all document types. Effective communicator with strong grammatical, written, and verbal skills. Dedicated work ethic, highly motivated, detail oriented, and adaptability to contribute to the growth of your company.

Highlights:

• San Diego, CA
• GLP
• GCP
• cGMP
• Document Control
• Quality Assurance