FESTOS O. TAH, II

• Performs sterile manufacturing in a cGMP cleanroom environment (ISO 5, ISO 7, ISO 8).
• Manufactures sterile products accurately and in compliance with master batch records while adhering to department specific SOPs.
• Utilizes appropriate aseptic technique when performing tasks within the cleanroom.
• Operates all fill-finish and ancillary manufacturing equipment in order to deliver quality medication.
• Maintains an ISO classified environment through rigorous cleaning and disinfecting of the cleanroom in accordance with approved procedures.
• Assists with sterilization of components used in the manufacturing process.
• Performs essential calculations and completes thorough documentation.
• Methodically prepares work area and supplies prior to manufacturing.
• Performs transfer of products from the cleanroom to the Inspection and Labeling.
• Performs ancillary tasks and duties that support the manufacturing process such as, but not limited to, autoclaving, bubble point testing, material preparation, inventory accounting, organization of components, and various LEAN manufacturing tasks (6S, GEMBA, Kaizen).

· Interacted with other departments and supervisors that included CT, VV, QC & QA to identify issues and find the solutions.

· Followed, executed, & supported the Sterility Assurance Program by documenting, perfecting cleanroom procedures, disinfection, and other sterility assurance protocols.

· Executed & monitored the Aseptic Process Simulations (APS).

· Evaluated production processes to gain understanding of problematic steps and rectify issues.

• Supported on-time delivery of products through diligent monitoring of order statuses and proactive communication with stakeholders.
• Enhanced inventory accuracy by conducting regular audits and maintaining updated records.
• Assisted team members with resolving discrepancies or issues related to purchase orders, facilitating smoother transactions.
• Contributed ideas during team meetings which led to the development of innovative solutions for common supply chain challenges.
• Participated in continuous improvement projects aimed at enhancing overall supply chain performance and delivering better value for the organization.

• Maintained quality documentation and records for conformance with relevant standards.
• Collaborated with production teams to address and resolve quality concerns, improving overall product reliability.
• Inspected raw materials and finished products to verify quality and disposed items that did not meet safety requirements.
• Evaluated samples against standards by completing measurements, visual inspections, and other established tests.
• Proposed corrective actions to address recurring quality issues.