Aaron Patrick Bury Email & Phone Number

Basel, Bs, Ch

New York, New York, Us

Maintained manufacturing operations on the production floor for filtration equipment, glass washers and autoclaves.Executed issue resolutions associated with process equipment commissioning, qualification and validation.Executed timely review of daily documentation and data entry, monitored, identified and communicated process and compliance trends and implemented any audit observation improvements.Controlled documentation of SOPs, manufacturing batch and formulation records and forms. Aided the Subject Matter Expert for manufacturing operations to support QTS investigations and CAPA implementations.Supported the implementation of Standard Operating Procedures (SOPs) for unit operations including Clean-In-Place, Steam-In-Place and Sanitization.Supported Lean Manufacturing, Sustainability, Operational Excellence initiatives.Facilitated the drive towards continuous improvement in all manufacturing areas.Remained current on training programs which supported manufacturing processes.Escalated process to management when operations, personnel safety, equipment functionality, product supply or quality compliance were at risk.Performed inventory reconciliation and task prioritization to maintain metric adherence.

Burlington, Ma, Us

Setup and used automated conveyor-style bottling operations which incorporated filamatic devices in addition to automated capping and labeling machines.Trained in aseptic technique and advancing hygiene standards associated with sterile fills and High Throughput System environments.Processed suspension-style fills requiring the use of mixing devices.Responsible for the setup and operation of peristaltic devices, pipettes, autoclave and lyophilizer technologies.Used SAP software system to comply with drug serialization and reporting requirements.Responsible for the use of forced air and supplied air respirator devices in the filling of hazardous materials.Conducted routine safety evaluations of the workspace including participation in the 5S system and implementation of corrective actions when needed.

Dublin, Ireland, Ie

Processed and refurbished containers that had been used for the containment of radioactive pharmaceuticals in order to maintain safety standards in place.Maintained tracking records including the intake and output of materials successfully.Ensured compliance with all regulations and safety precautions regarding the handling of radioactive materials including the use of Geiger counter devices.

Aided the production and filtration of materials and compounds used in the creation of pharmaceuticals and laboratory research applications.Worked under the regulation of the Food and Drug Administration and adhered to the strictures established by Good Manufacturing Practices . Used Standard Written Procedure and scientific notation as a template for documentation required during production, sampling, testing and cleaning validation.Worked on the factory floor, aware of the safety protocols and demands of working in a warehouse environment.