Leira Carrion Email & Phone Number

United States

Rockville, Maryland, United States

• Assist with scheduling of calibration/preventative maintenance for equipment and labinstruments.
• Review contractor documentation for services provided.
• Coordinate and oversee all building preventive maintenance activities and identify, schedulesand communicates the work to be performed with other departments to avoid interruptions in manufacturing.
• Perform and/or review calibrations of laboratory instruments and GMP equipment (e.g.,chromatographic systems, balances, freezers).
• Enroll new equipment and systems by following establish procedures for procurement andenters new equipment data in the calibration tracker to schedule, track and document calibrationand maintenance work to be performed.
• Assist as needed to monitor vendors while working onsite and updates equipment logbooks forthe work being performed. Reports deficiencies with maintenance and activities of equipmentand recommends areas for improvement.

• Assist with scheduling of calibration/preventative maintenance for equipment and lab instruments.
• Review contractor documentation for services provided.
• Coordinate and oversee all building preventive maintenance activities and identify, schedulesand communicates the work to be performed with other departments to avoid disruptions in manufacturing activities.
• Perform and/or review calibrations of laboratory instruments and GMP equipment (e.g.,chromatographic systems, dissolution units, balances, stability chambers).
• Enroll new equipment and systems by following establish procedures for procurement andenters new equipment data in the calibration tracker to schedule, track and document calibrationand maintenance work to be performed.
• Assist as needed to monitor vendors while working onsite and updates equipment logbooks forthe work being performed. Reports deficiencies with maintenance and activities of equipmentand recommends areas for improvement.

Rockville, Maryland, United States

• Contribute to the creation and revision of Batch Records, Deviations, Work Instructions, Standard Operating Procedures, Material Specifications, and other GMP documents.
• Adhere to all SOPs and executed batch records under GMP regulations documenting all manufacturing activities clearly and accurately, including preparation records, testing records, and equipment logbooks.
• Maintain adequate supplies and performed routine equipment maintenance.
• Use Blue Mountain to manage preventive maintenance, work orders, and calibrations.
• Participate in client and regulatory audits, hands-on production in the manufacturing of material for clinical trials in a GMP environment by conducting purification operations including filtration, chromatography.
• Follow all related safety rules and procedures when working with hazardous materials.

Hanover, Maryland, United States

• Processed, packaged, and shipped orders accurately
• Ensured that stocks and inventory are well-organized and maintained
• Examined and inspected products for defects and damages
• Discharged duties in strict compliance with amazon safety and hygiene regulations
• Actively participated and contributed ideas on ways to improve and/or optimize warehousing procedures
• Followed the state health and safety regulations and practices

• Distributed specimens, accessioned and performed other functions to ensure optimal functioning of laboratory operations.