Seeking an Advanced Position to apply my relevant experience to benefit the manufacturing team and further my development in the biotechnology industry.
Overview
4
4
years of professional experience
Work History
Sr. Manufacturing Associate Formulation
Takeda
11.2020 - Current
Responsible for aseptically producing bulk formulation product
Dispensing chemicals and preparing buffers
Implement processes in production while strictly following cGMP, environmental health and safety guidelines and any other related regulations
Clean, operate, and teardown of equipment such as, tanks, filtration systems, filling lines
Operate general production equipment such as an autoclave, filter integrity testers, temperature probes, pH and conductivity meters, CIP skids
Receive and distribute supplies into the manufacturing areas
Review batch records and electronic records
Redline and edit SOPs
Currently Interim Lead for 1 year.
Exceeded daily production targets with consistent attention to detail and commitment to meeting deadlines.
Collaborated effectively with cross-functional teams to troubleshoot issues, optimize processes, and achieve common goals.
Supported the implementation of new procedures or systems within the facility, adapting quickly to changes while maintaining high-quality output levels consistently.
Organized and prepared workstations and materials needed for operations to maximize productivity.
Made sure that products were produced on time and are of good quality.
Manufacturing Associate Cell Culture
Takeda
05.2020 - 11.2020
Support Cell Culture operations for the production of a bulk drug substance product
Prepare media and buffer solutions
Clean, Set up, operate, and teardown of equipment such as tanks, filtration systems, carton assembler, bioreactors, and production lines
Operate filtration systems such as harvest cart and media cart.
Operation and cleaning of biosafety cabinets.
Operate general production equipment (such as pH and conductivity meters, autoclave, portable mixers, etc.)
Monitor and record critical process parameters
Complete relevant paperwork following GDP/GMP guidelines
Perform routine maintenance and cleaning of production equipment to maintain equipment in GMP fashion
Manually clean portable equipment and small parts
Perform sampling using aseptic techniques
Participate on Continuous Improvement Teams (improving our tier board)
Receive and distribute supplies into the production area as necessary.
Utilized hand tools and machinery to safely complete assembly processes.
Met production targets and tight deadlines by collaborating closely with team members.