Coach manufacturing associates and serve as SME on Cell Cultureand Upstream processes, human performance initiatives,identifying risks, and implementing mitigation strategies.Lead team initiatives, aligning objectives with company goals andconsistently meeting production timelines.Drive continuous process improvements by assessing workflows,implementing enhancements, and collaborating with cross-functional teams.Enforce safety protocols, reducing risks and ensuring complianceacross various clean room classifications (ISO 5-8).Collaborate with supporting teams to troubleshoot hardware andsoftware issues, enhancing equipment performance and gainingoperational insights.Initiate vial thawing and media distribution in ISO 5 (Class 100)environments, facilitating the inoculation process and promotingcell growth in incubators.Document and maintain GMP data, deviations, process steps, andcritical documentation like batch records and logbooks to ensureaudit readiness.Work closely with Quality Assurance to resolve documentationdiscrepancies and ensure adherence to GDP and regulatorystandards.Lead initiatives to assess workflows, implement safety, quality, andefficiency improvements, and drive continuous enhancement ofprocesses.

Facilitated the centrifugal and filtration processes to isolate targeted cell structures and proteins.Monitored and controlled process parameters such as pH level, temperature, and pressure.Executed process operations within cGMP standards, operating equipment, analytical equipment and performing validation protocols.Took initiative in leading time sensitive operations, including sampling analysis and coordination with upstream processes.Implemented preventative measures to streamline processes and increase efficiency.Trained team members through hands on demonstrations and clear communication, improving overall production capacity.Documented and recorded GDP data, including process steps, deviations, and equipment activities to maintain compliance.Managed inventory control, and work orders to optimize manufacturing operations.Adapted quickly to changing conditions during manufacturing, ensuring agility and responsiveness throughout the process.

Cultivated relationships with brokers, shippers, and manufacturers, ensuring seamless communication and operations.Acted as the primary liaison between logistics partners and drivers, coordinating and resolving transportation issues and time delays.Developed and adhered to a strict maintenance schedule for the fleet, ensuring vehicles were operational and FMCSA compliant.Administered payroll for all associates and managed all accounting functions, including expenses, reconciliation of receipts and tax documentation.Ensured compliance by maintaining and organizing key filings such as LLC, FMCSA, and UCR.Authorized all purchasing decisions, maintenance activities, and fuel card management for the fleet.Directed marketing and social media efforts to promote the organization and increase brand awareness.

Supervised recording and visual projects, operating software such as Logic Pro X, Pro Tools, FL Studio, and Adobe Creative Suite.Used frequency sculpting, and transient compression of achieve commercial quality audio.Troubleshooted audio hardware such as mixing boards, audio interfaces, preamps, condenser microphones.Created visuals and artwork for audio projects, managed website and social media platforms, and spearheaded marketing campaigns.Negotiated deals, processed transactions, and promoted a productive environment for interns and employees.Collaborated with the Quality team for product releases and delegated team responsibilities while addressing documentation and audio quality improvements.

Operated within clean room environments, maintaining wafer lab tools and ensuring air particle control.Managed documentation and data recording for processing steps and equipment activities.Communicated effectively with management and team members to resolve issues and enhance cross- functional interactions.