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• Manage a team of associate scientists to execute manufacturing plans.• Responsible for managing the work of production by establishing good communication within the team/Operations so that schedules are clear and aligned with priorities.• Responsible for all equipment calibration scheduling and maintenance.• Ensure proper lab practices are followed, including work in biosafety hoods, gowning, and routine decontamination processes of manufacturing suites and work environment is safe and efficient.• Manage NPI, process improvements, and internal investigations.• Train new hires on production processes & ensure training is adherence to quality assurance standards.• Perform employee calibration, discuss PMDs, employee end of year review, and comp planning.• Collaborate with IT, QA, PMs, and R&D to investigate customer complaints and root cause analysis.• Comply with manufacturing quality standard: Problem Record, Planned deviation, NCM, ECR.• Monitor and maintain flawless manufacturing system migration from NetSuite to SAP.• Issue batch records, transact work orders and manage material transfers in ERP system• Ensure manufacturing batch records, SOP/WI procedures accurately reflect current processes. Initiate change orders as necessary. • Organize and maintain efficient build room layout to ensure ease of use and cleanliness.• Participate in ISO13485 annual audits.

• Manage a team of 70 manufacturing operators to provide support to manufacturing workflow.• Perform employee calibration, discuss PMDs, employee end of year review, and comp planning.• Maintain, monitor, and communicate Tier metrics for manufacturing department.• Collaborate and establish strong relationship amongst IT, QA, and Engineer support groups.• ISO13485 Manufacturing quality standard.• Expert in generating and investigating problem records (PR) using TrackWise.• Promote Site Safety regulations and programs maintain company’s VPP status.• Facilitate PPI Kaizen continuous improvement workshops.• Encourage individual and team development to increase team morale.• Generate, monitor, and approve changes to department Standard Operating Procedures (SOPs).• Interact with vendors to ensure all lab equipment completed preventative maintenance & calibration.• Conduct monthly mock audit and effectiveness checks on manufacturing procedures to ensure completion of batch records and capture and correct any deviations.• Subject matter expert in large scale RNA synthesis, purification, and InVivo processing.• Responsible for incoming complaints and conduct thorough investigation to determine root cause.

• Tracked and monitored high volume of inbound and outbound shipments with vendors.• Maintained compliance with related regulations, policies and procedures. • Received and evaluated incoming specimen shipments against incoming material specifications to identify areas of non-compliance.• Retrieved specimens for distribution to laboratories packaged per applicable regulations and delivered in accordance with SOPs. • Responsible for management and record keeping of inventoried finished goods with SAP-LIMs system.• Executed record keeping in compliance with good documentation practices to ISO 9001 standards.

• Supervised and Lead a team of 40 employees.• Maintained process work flow and organization throughout work shift.• Trained operators on synthesis on detailed laboratory processes using SOPs and WINs.• Coordinated and executed cross-training plan for employees.• Provided safety on-boarding procedure for new hires.• Communicated and collaborated with QA, Service, and IT support group.• Subject matter expert in DNA & RNA oligonucleotide synthesis.• Oligonucleotide synthesis using Jurassic J96U and MerMade12.• Performed RNA InVivo purification.• Performed purification process using AKTA Explorer using Unicorn & Alliance HPLC waters system using Empower 2 Pro.• Performed oligonucleotides purification analysis on Agilent HPLC using ChemStation• Perform QC Mass Spec on Voyagers and CE taces analysis on Combisemp• Data analysis using Spectrophotometer via SpectraMax.• Monitored and troubleshoot equipments that require calibration and maintenance.• Collaborated with site EH&S to comply with OSHA regulations and standards.• Actively in involved in Continuous Improvement & Process Excellence: PPI, Kaizen, 6S, and hazard ID. • Experience in CAPAs, PRs, NCMs, GDP, and GMP.• Complied with ISO 13485 oligomanufacturing standards.• Composed and revised SOPs and WINs.

• Performed DNA collections via mucus samples.• Collected hair samples for drug tests.• Performed daily calibration and quality control.• Prepared standard chemical solutions and reagents.• Troubleshoot and find solutions to malfunctions or anomalies.• Trained and monitored new employees.• Clean and organize to maintain a clean work space and environment.• Cooperated with San Jose Probation department through prop 36.• Back up test results to database at end of shift.• Sent daily updates and results to head quarter and the probation department.• Certified lab tech to operate a high performance immuno-analyzer – Olympus-AU680.• Prioritize important work tasks and manage work time; exemplary multi-tasking skills• Environmental monitoring - analyzed, interpreted and reported test results via urinalysis.• Disposed & document bio-hazardous material post sterilization.

• Supervised and managed a team of 20 staffs and volunteers.• Coordinated San Jose After-School program serving “at-risk” students.• Collaborated with Franklin-McKinley, Evergreen, and Alum Rock School Districts. • Provided yearly demographic reports to the City of San Jose.• Recruited and interview employees and volunteers.• Organized fundraising events to raise money for next fiscal year. • Arranged meetings, conferences, and travel itineraries.• Performed data input & maintains established databases.• Maintained confidential program files & records.

• Screened new employee potential to perform work task.• Trained new hire employees.• Pre-uploaded and post-downloaded Teflon, ions, quarts, and SO2 filters.• Collected varied air quality samples from specific locations throughout United States.• Prepared slides of filters for analysis.• Performed physical analyses of returned collected filters.• Removed static and particles from filters using polonium strips.• Handled sensitive CAHN balance to weigh Teflon filters.