Responsibilities: of the Quality Assurance Specialist I include: · Perform raw data, critical study phase, facility, study protocol, and final report audits in accordance with GLP requirements · Report audit and inspection findings to Study Directors and Testing Facility Management · Maintain quality assurance records, audit status reports, study protocols, amendments, and related QA documentation · Assist with regulatory inspections, site visit preparation, document control, archival activities, and SOP management Qualifications: for the Quality Assurance Specialist I include: · AS or BS degree in Biological Sciences, Regulatory Sciences, or a related field with at least 1 year of technical or quality experience · Experience in a regulated laboratory environment; GLP experience preferred · Ability to review scientific documentation, communicate audit findings, and work independently or within a team environment Compensation: for Quality Assurance Specialist I includes: · $25-$35/hr depending on experience · Comprehensive Benefit Package: Cigna Medical/Dental/Vision, 401K, Sick Leave as Required by Law This job is open for applications on September 21st, 2026. Applications will be accepted at least 30 days from the posting date.
| Location | Rockville, MD |
| Salary | $25–$35 Per Hour |
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