Jamil Bost

• Played an active role during emergency response situations by following established protocols and applying critical thinking skills under pressure.
• Trained new operators in correct operation procedures, ensuring consistent performance across shifts.
• Participated in regular safety training sessions to stay current with industry best practices and reinforce company-wide commitment to safety excellence.
• Prepared detailed shift reports for management review, providing insight into daily operations, incidents, or deviations from normal conditions at the facility.
• Collaborated with research and development teams to test new processes or technologies, providing valuable feedback for potential scale-up to full production capacity.
• Ensured safety compliance with strict adherence to industry regulations, company guidelines, and proper handling of hazardous materials.
• Stored, retrieved, mixed, and monitored chemicals used in production process.
• Operated lab equipment for chemical tests and verification of product quality produced during run.
• Used panel boards, control boards and semi-automatic equipment to control or operate chemical processes and systems of machines.
• Demonstrated flexibility and adaptability in the face of changing production demands, seamlessly transitioning between tasks as needed to support overall efficiency.
• Operated manual pallet jacks and forklifts to move and store materials.
• Sealed products by applying appropriate fastenings and ties and confirmed seal integrity to prevent product and packaging damage.
• Maintained optimal equipment performance by carrying out simple hourly maintenance on machines.
• Reduced production downtime 40% through quick problem-solving and rapid equipment repairs, eliminating excessive use of outside repair vendors and overtime.

• Upheld strict quality standards throughout all stages of production, resulting in consistently reliable medical devices for end users.
• Carry out troubleshooting efforts for equipment malfunctions or process anomalies within the cleanroom facility, contributing experience in problem resolution efforts.
• Demonstrated adaptability by quickly mastering new techniques and technologies introduced in the workplace: performed in the role as Subject Matter Expert for 5 of 10 processes.
• Managed and monitored processes and machine systems by observing readings on control boards.
• Optimized inventory management by accurately tracking component usage and maintaining proper stock levels for essential parts.
• Aided in the development of new processes by collaborating with cross-functional teams on continuous improvement initiatives.
• Supported quality control efforts through accurate documentation of batch records, equipment logs, and other essential data.
• Reduced downtime for maintenance by performing regular inspections and preventative measures.
• Maintain GMP cleanliness to ISO 5 & 7 cleanrooms: autoclaving, removing of hazardous & nonhazardous waste, and organization.
• Trained new hires as well as existing staff on various processes.
• Perform detailed in-process inspection of medical devices: determine if product is acceptable. Initiate Non Conformance Reviews on any product outside of conformance.
• Provided technical support during process audits, ensuring adherence to regulatory requirements.
• Maintain and be responsible for the calibration and maintenance of high precision inspection tools.
• Provide hands-on support to internal and external Repair staff during equipment install projects.
• Examined incoming materials and compared to documentation for accuracy and quality.
• Completed other duties as assigned.

Performed functions related to the processing of FDA approved drug products, ensuring product compliance to established current Good Manufacturing Practices.

• Examine manufacturer product labels, Quality Control release tags, and Batch Production Records to verify issued/ staged raw materials are ready for release.
• Operated pharmaceutical production machinery and followed the procedures for manufacturing such as thaw, weighing, blending, fill, and stage.
• Assisted in troubleshooting equipment issues, minimizing downtime to keep production on track to meet deadlines.
• Monitored the manufacturing processes and implemented control factors to keep production within acceptable limits.
• Cleaned manufacturing rooms and equipment per SOP's.
• Identified potential process improvements for the department.
• Worked with engineers and Shift Leads to resolve line issues and initiate line clearances,
• Completed documentation associated with manufacturing processes with detail and accuracy.
• Maintained up-to-date statuses on all job related training modules.
• Execute machine changeovers from batch to batch.
• Completed environmental monitoring prior to shift production.
• Adhered to aseptic gowning and all cleanroom expectations.
• Sampled batches for quality assurance; executed in- process product quality checks and documented accurately.
• Participated in continuous improvement projects of moderate scope.
• Participated in shift huddles, safety teams,5S projects, etc.
• Other duties as assigned.