Michael Maglio Email & Phone Number

Fremont, NH, US

Bedford, New Hampshire, United States

Oversee eight direct reports within the QC Microbiology team, providing technical expertise and mentorshipParticipated in the authoring and review of quality event documents (Events, CAPAs, Deviations, Investigations, RCAs), as well as performing peer review of assay documentation and resultant data.Scheduling laboratory work for multiple shifts, and.

Performed quality control data review tasks, supporting the development of live microbiome pharmaceuticals. Participated in the authoring and review of quality event documents (CAPAs, Deviations, Investigations, RCAs).Engaged in regular meetings and collaborative projects interdepartmentally, as well as with external contractors.

Salem, New Hampshire, United States

• Performed microbial identification methods (MALDI/PCR/qPCR) on dozens of bacterial and fungal samples daily.
• Authored and reviewed deviations, investigations, root cause analyses (RCAs), and corrective and preventive actions (CAPAs) for laboratory events, to ensure compliance with regulatory standards and maintain the highest.
• Actively participated in the safety committee by reviewing safety plans, conducted monthly safety inspections, and participating in safety meetings with 10+ members, which resulted in expedited response times in.
• Spearheaded the modification of ELN templates in LIMS to automate calculations which eliminated daily recurring error in documentation, receiving recognition and praise from clients.
• Played a pivotal role as a qualified trainer by coaching 6 new analysts to ensure that they are equipped with the necessary knowledge and skills to perform their jobs with the highest level of excellence and acting as.
• Launched a new system for logging in Microbial ID projects which reduced redundancy and improved turnaround time by 1-2 days per project (50% reduction in TAT).

• Performed in-depth data analysis from the SHIFT cohort study on occupational epidemiology in healthcare facilities to pinpoint the root causes and outcomes of low back pain among healthcare workers.
• Translated complex statistical analyses into easy-to-understand presentations for non-technical audiences, including survey sites and funding agencies as well as to highly technical audiences such as NIOSH and CPH-NEW.

Marlborough, Massachusetts, United States

• Managed DNA sample processing for ancestry genetics, overseeing all aspects of DNA extraction, purification, and Illuminasequencing, with a record of successfully processing over 2,000 samples per week.
• Streamlined sample processing by automating liquid handling equipment (Tecan and Hamilton) and large quantity samplecapper/decappers (Sarstedt), utilizing associated software to ensure the accurate set up and.
• Adhered to strict SOPs and safety guidelines, including OSHA standards for bloodborne pathogens and standard precautions tomaintain a safe and compliant laboratory environment while handling human samples.

• Interacted with 8+ patients daily to provide quality emergency care and educated patients on medical procedures and recommendations while maintaining a kind, compassionate, and polite demeanour.
• Took vital signs and completed detailed reports on patient medical history, medications, and current state to help provide anaccurate diagnosis, determine indications or contraindications for medications, and.
• Collaborated with 10+ paramedics and a Medical Director to manage advanced life support cases.
• Maintained up to date on NREMT care protocols and standards by successfully completing over 80 hours of continuing educationand professional development courses every 2 years.
• Maintained an organized, clean, and well-stocked ambulance by proactively analyzing inventory levels and replacing missing, damaged, or expired supplies.

Bedford, Massachusetts, United States

• Performed pre-clinical biocompatibility and toxicology testing for pharmaceuticals and medical devices.
• Protocols for each device and drug were developed in accordance with standard procedures outlined in the USP and regulated bythe USDA and FDA.
• Utilized in-vivo (lab animals) and in-vitro (blood analyses) to determine whether the devices and drug products were safe to usewhen in contact with a living system; devices were tested directly via surgical implants.

Master Of Public Health - Mph, Epidemiology

NIOSH Trainee

Bachelor'S Degree, Biology/Biological Sciences, General