Work History
Overview
Timeline
Generic

CARLOS WEBB

Scientist
Atlanta,Georgia

Work History

Sr. Tech Development Research Specialist

TAKEDA Pharmaceutical
Covington
07.2020 - Current
  • Oversaw recruitment and termination processes for research chemists
  • Completed semiannual and annual reviews for a team of five scientists
  • Develop and maintain project schedules, ensuring milestones are met
  • Train junior researchers on laboratory techniques, safety protocols, and data analysis
  • Collaborate with stakeholders (R&D, manufacturing, quality) to align project goals
  • Conduct process optimization studies to enhance yield and purity
  • Communicate project updates and results to management and cross-functional teams
  • Investigate deviations and implement corrective actions
  • Managed resources effectively, leading a team of ten to achieve project objectives
  • Assisted in the development of novel fractionation methods
  • Conducted experiments to optimize process parameters
  • Collaborated Quality audits in production areas, from CIP to Final container
  • Testing and analyzing microbiological results from CIP studies
  • Yellow Belt (Lean Six Sigma) Certification.

Tech Development Research Specialist II

TAKEDA Pharmaceutical
Covington
07.2018 - 06.2020
  • Process Development: Expertise in designing and optimizing bioprocesses, including immunoglobulin purification and fractionation
  • Analytical Skills: Proficient in HPLC, SDS-PAGE, ELISA, and other analytical techniques
  • DOE Knowledge: Experienced in experimental design and statistical analysis
  • Laboratory Proficiency: Skilled in executing experiments, data analysis, and troubleshooting
  • Time Management: Ability to prioritize tasks and meet project deadlines
  • 5S Implementation: Maintain a well-organized and efficient laboratory space
  • Cross-Functional Collaboration: Work effectively with R&D, manufacturing, and quality teams.

Quality Associate III (Lead Chemist)

SHIRE PHARMACEUTICAL
Covington
08.2014 - 07.2018
  • Green Site, implementation of most of the QMS, and Quality processes
  • Oversee quality control laboratory operations, managing a team of chemists
  • Perform routine analysis of raw materials, active ingredients, and finished products
  • Troubleshoot HPLC, GC, and other instruments to ensure accurate testing
  • Collaborate with cross-functional teams to address quality-related issues
  • Train new chemists on instrumental testing techniques and protocols
  • Prepare and review test procedures, SOPs, and protocols
  • Maintain compliance with FDA regulations and company standards
  • Contribute to continuous improvement initiatives for process efficiency
  • Conducted analytical testing on biopharmaceutical products.

Senior QC Analyst

ALKERMES
Gainesville
01.2014 - 08.2014
  • Responsible for using HPLC to determine the concentration and identification of unknown samples solutions by comparing against known standards
  • Used GC to determine the level of residual solvents that may be present in a drug product after manufacturing process
  • Skilled with the use of dissolution systems to determine the release profile of a drug product over time
  • Designed and monitored clinical research trials on extended-release rate of transdermal patch
  • Collects and process data from clinical trials to determine efficacy of product.

Quality Assurance Analyst II

THE COCA-COLA CO. (TCCC)
Atlanta
10.2005 - 02.2013
  • Managed a team of over 10 chemists across two shifts, overseeing daily operations and coordinating training objectives
  • Successfully implemented Operational Excellence practices throughout the laboratory and manufacturing facility
  • Knowledgeable of food safety regulations (USDA, FDA), and quality management systems
  • (HACCP, GMP) Ensured timely delivery of results for raw materials, semi-finished products, finished goods, and treated water
  • Conducted visual inspections of packaging materials, assessing weight, density, stress, dimensions, torque, and strength
  • Proficiently set up and operated HPLC equipment for various experiments, including size exclusion, ion exchange, and reverse phase analyses
  • Utilized GC techniques to verify whether ingredients and finished products met company specifications
  • Developed solutions for distressed and problematic batches, minimizing production losses
  • Played an instrumental role in obtaining ISO 17025 accreditation for the laboratory
  • Identified, conducted, and led opportunities to enhance quality, reduce costs, and improve process efficiency
  • Proficiently performed RCA and CAPA investigations to identify and rectify process issues
  • Created and revised specifications, standard operating procedures (SOPs), and other relevant documents for quality control operations
  • Thrived in a manufacturing environment with tight deadlines and cross-functional dependencies.

Overview

19
19
years of professional experience

Timeline

Sr. Tech Development Research Specialist

TAKEDA Pharmaceutical
07.2020 - Current

Tech Development Research Specialist II

TAKEDA Pharmaceutical
07.2018 - 06.2020

Quality Associate III (Lead Chemist)

SHIRE PHARMACEUTICAL
08.2014 - 07.2018

Senior QC Analyst

ALKERMES
01.2014 - 08.2014

Quality Assurance Analyst II

THE COCA-COLA CO. (TCCC)
10.2005 - 02.2013

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CARLOS WEBBScientist