Organized and detail oriented professional with almost 3 years of clinical Quality Assurance/ Quality Control experience in a regulated GMP environment. Good communication and problem solving skills, adept at managing multiple projects. Authored multiple Standard Operating Procedures (SOP), Qualification Protocols and Methods. Acted as the de-facto supervisor of the QA team for the last 5 months. Supervisory responsibilities include, managing QA department and mentoring new QA staff. Pursuing opportunity to expand on current work experience of Quality Assurance and knowledge of clinical research trials.

Highlights:

• Auditing
• Batch Production Record
• CMC
• SOP
• Qualification Protocol
• Data trending
• Clinical
• Quality