Brittany Dias Email & Phone Number

Hartford, Ct, Us

Windsor, Connecticut, United States

• Navigate MasterControl, Sage, Avigilon and DocLink systems to intake, investigate, and author over 250 logistic, product and adverse drug event (ADE) reports in accordance with quality system guidelines and timeframes. • Liaise between system owners to identify SOP and cGMP deviations for root cause determination and corrective action implementation. Monitor corrective action implementations for efficiency and adherence to timeline commitments.• Track and trend complaint receipts to generate metric reports on a monthly, quarterly and yearly basis. • Lead departmental meetings between system owners and senior management for trend awareness and correction. • Assist in data and document procurement as required for internal, external, and FDA audit conductions. • Notify and communicate with state regulatory officials in fulfillment of mandated reporting guidelines. • Facilitate company adherence to federal reporting timelines. • Communicate preliminary and final investigation findings with customers via phone, email and written correspondence. • Review and update SOPs, position papers and other documents per company needs. • Inspect returned and reserve drug product units related to complaint investigations. • Coordinate the timely submission of drug product testing by internal and external laboratories according to BUD.

Ellington, Connecticut, United States

• Execute regulatory testing of products to ensure compliance with FDA and contract packager standards. • Create and maintain accurate records of product specifications to identify and reduce deviations from quality control standards. • Perform analytical inspections of production machinery for conformance to sanitation parameters. • Conduct daily audits of product packaging and coding to verify production and product integrity. • Liaise between production, laboratory, and administrative staff to successfully meet organization needs and quotas.• Enforce current good manufacturing practices (cGMPs) to ensure employee and consumer safety.

Hartford, Connecticut, United States

• Partnered with Aetna, a CVS Health Company, to translate STEM concepts and teach SAT preparation strategies to 30 young women, ages 13 to 18, from the Hartford County Region.• Created, administered, and evaluated 30 weekly pre- and post-tests.• Utilized MS Excel to analyze participant growth later used to acquire grant funding for future youth programs.• Planned and co-facilitated learning activities to further summer youth development in an afterschool setting.

Department Of Animal Science; Reed Lab, Storrs, Ct

• Advanced aseptic culturing of proliferating and differentiated mouse myoblast and carcinoma cells.• Analyzed and translated elaborate research results to concise, academic website descriptions for non-experts.• Spearheaded method of proteomic protein data arrangement to present research results using MS Excel and Word.• Collaborated on extensive animal oxidative stress research experiment.• Co-presented oxidative stress research data at 2019 American Society of Animal Science Conference in Austin,TX using acquired Louis Stokes Alliance for Minority Participation (LSAMP) scholarship funding.

Department Of Physiology & Neurobiology; Storrs, Ct

• Co-managed department email correspondences.• Prepared and distributed graduate school promotional media.• Arranged and maintained graduate school information management systems using MS Excel and Word.• Faxed and photocopied office correspondences.• Greeted and directed visitors to their appropriate, designated destinations.