Anna Greer Email & Phone Number

Waltham, Ma, Us

Progressing through various roles of increased responsibilities, I was selected to oversee quality assurance and facility audits, including GxP compliance, quality auditing, risk management, root cause analysis, audit scheduling, and project coordination.Key achievements and contributions during this tenure include:➤ Providing expert oversight during in-process and facility audits, including operational monitoring, strategic planning, and team guidance, I refined quality assurance practices, increased audit accuracy, and reduced non-conformance rates.➤ I prevented regulatory fines and penalties by performing inspections, updating project supervisors on evolving industry requirements or changes, and conducting tailored training sessions that led to zero compliance violations during audits.➤ I provided hands-on support and expertise during complex audits to ensure positive audit outcomes. This included resolving intricate compliance issues and facilitating corrective actions to support internal and external audits.➤ I implemented targeted process improvements, standardized audit procedures, established new policies, and automated routine quality checks that helped reduce audit review time, improve reporting accuracy, and enhance efficiencies.➤ I enhanced audit preparation and execution by coordinating with project teams and principal investigators to ensure audit readiness. This involved conducting pre-audit briefings and creating a checklist to address any last-minute issues.

Wilmington, Nc, Us

As Quality Assurance Auditor II, I monitored, controlled, and optimized laboratory processes, procedures, and products. This involved conducting protocol reviews, leading process audits, delivering insightful data analysis, training new auditors, and creating quality assurance frameworks. Furthermore, I inspected raw materials and identified any deviations from quality standards to maintain the highest product safety and efficacy levels.Key achievements and contributions during this tenure include:➤ I developed comprehensive internal audit programs, conducted in-depth protocol reviews, and delivered interactive training modules on quality assurance policies, FDA regulations, GMP standards, and SOP adherence.➤ I optimized quality metrics by leading continuous improvement initiatives. This involved analyzing audit data and industry trends, identifying key areas for enhancement, and implementing action plans that addressed root causes of non-compliance.➤ I minimized customer complaints and improved product quality by identifying pain points and improvement opportunities using a robust feedback mechanism, including detailed surveys, follow-up reviews, and customer engagement.➤ I increased employee performance and engagement by delivering individualized feedback during training sessions, which increased job satisfaction, retention, and productivity through development plans and clear performance expectations.➤ I reduced the time required for protocol reviews and audits by implementing process improvements, including streamlined review procedures, enhanced documentation practices, and autonomous tools. ➤ I expanded department audit capacity by revamping facility audit workflows, incorporating innovative approaches and lean principles, and reallocating resources. This resulted in faster turnaround times without compromising audit quality.

Wilmington, Nc, Us

In this role, I managed in-process specimen, assay, and facility audits to ensure compliance with quality standards, including document management, quality assurance procedures, reporting, cross-functional collaboration, and process improvement. Developing auditing schedules and organizing departmental materials, I drove operational efficiencies and supported audit processes.Key achievements and contributions during this tenure include:➤ I increased compliance with regulatory standards and enhanced data integrity by conducting in-process audits for specimen storage and assay processes (PK, ADA, CLIA) to identify and address potential issues for maintaining high-quality standards.➤ I enhanced departmental organization and efficiency by systematically archiving obsolete materials and optimizing the storage of essential documentation. This resulted in improved accessibility and reduced retrieval time for critical records.➤ I audited supplier processes, identified root causes of defects, and implemented targeted corrective actions to improve supplier quality. This led to reduced supplier defects and increased product consistency across multiple batches.➤ I drove cross-departmental collaboration by facilitating quality meetings and creating a shared platform for issue tracking and resolution. This involved establishing and fostering a culture of continuous improvement and accountability across teams to increase productivity.

Wilmington, Nc, Us

This role involved, performing comprehensive audits of analytical and validation data, reports, and methods, ensuring adherence to regulatory and compliance standards in the pharmaceutical industry. Also, I managed the workflow of QA documentation, maintained a chain of custody for laboratory materials, and effectively communicated and escalated any anomalies to QA management for quick resolution.Key achievements and contributions during this tenure include: ➤ I increased stakeholder satisfaction by consistently meeting audit deadlines, providing detailed and timely updates on audit progress, and proactively addressing stakeholder concerns through regular communication and tailored feedback sessions.➤ I created a comprehensive, standardized checklist that reduced audit preparation time. This involved streamlining document collection and developing detailed training materials to ensure consistent audit readiness across departments.➤ I facilitated better communication between audit teams and clinical staff by organizing bi-weekly debriefing sessions post-audit, which included reviews of audit findings, collaborative discussions, and enhanced clarity and faster resolution of compliance issues.➤ Leveraging advanced data analysis techniques, including trend identification and root cause analysis, I improved audit reporting accuracy and delivered actionable insights and findings to support stakeholders' decision-making.

Wilmington, Nc, Us

Richmond, Virginia, Us

Tasks Isolated DNA plasmids centrifuged samples Performed restriction enzyme digests Conducted gel electrophoresis Observed cesium chloride extraction Laboratory Maintenance prepared reagents and buffers

Richmond, Va, Us

tasksassisted students and instructorsheld office hoursgraded assignments

Bachelor Of Science, Forensic Science, Forensic Biology Track

Bachelor Of Science, Mathematics, Biomathematics Track