Summary
Overview
Work History
Education
Skills
Accomplishments
Timeline
Generic

Joe Dominguez

Waco,TX

Summary

Solution-oriented Manufacturing Specialist with 10 years of experience. Committed to worker and workplace safety and cutting costs without sacrificing quality. Successful in problem-solving and critical thinking in times of stress.

Overview

9
9
years of professional experience

Work History

Manufacturing Technician

  • II, Compounding
  • Responsible for compounding high-quality solutions, semi-solids, and suspensions in accordance with Good
  • Manufacturing Practices (GMP) and department Standard Operating Procedures (SOP)
  • Accurate formulation of products
  • Stage, load, operate, and monitor all equipment for product formulations
  • Weighing and mixing chemicals according to specific formulas
  • Calibrate, operate, and monitor all formulation-related equipment (e.g., mixers, scales, meters, etc.)
  • Perform operations necessary to adjust the pH of product for in-process testing
  • Clean, steam, and sanitizes all tanks, facilities, equipment and chemical containers used in the product formulation process in accordance with current SOP s and cGMP s
  • Accurately complete documents and record production volumes (batches) in compliance with current GDP standards
  • Assumes other duties and responsibilities, as necessary, within the Compounding department, in an effort to provide the required support to ensure adherence to the production schedule
  • Manufacturing Operator III, Unit Dose Fill
  • Perform production line duties required to meet production goals while complying with quality standards and safety requirements
  • Operate production equipment and complete documentation in accordance with cGMP’s and department
  • SOP’s while monitoring product to ensure quality standards are maintained
  • This position is responsible for one or more of the following duties or activities (See individual department areas in this document for specific accountabilities):
  • Maintain a clean and organized work area during and at the end of each shift
  • Assist in achieving environmental, health, and safety goals by working safely and observing all general plant and department safety policies
  • Perform all assigned duties according to departmental SOP’s and cGMP’s
  • Remain current on proper procedures by reviewing current, revised, and new SOP’s relating to the job and to the department
  • Complete and remain current with all required cGMP and safety training
  • Perform tasks in the production / packaging of product to provide on-time delivery to customers
  • Complete all required documentation associated with the production and / or packaging of product
  • Assist daily production in operating and monitoring technical, computerized, production machinery, ensuring quality standards are maintained
  • Regulated Responsibilities (including cGMP and EHS)
  • Incumbent is expected to be fully compliant with all criteria established by governmental agencies, Ministry of Health, and legislative requirements including, but not limited to: the FDA, European Community (EC),
  • ISO 13485 - Medical Devices, European Economic Community Medical Device Directive (MDD), Canadian
  • Medical Device Regulations (CMDR), OSHA, Sarbanes-Oxley, EPA, DOT, EEOC, and ADA
  • Incumbent will work to ensure that the company is in compliance with all environmental, health and safety requirements and assure our business practices enhance the welfare of our customers, employees and the community in which we operate, II, MD Fill Room/Sterile Room
  • Perform inspections of products and pulls Quality Assurance samples for Microbiology and Chemistry testing
  • Perform aseptic interventions on equipment
  • Remain manufacturing processes and procedures by reviewing current, revised, and new SOP’s relating to the job and department
  • Complete and remain current on all required cGMP and safety training
  • Assist Maintenance Technicians with basic mechanical adjustments as needed
  • Complete all required documentation associated with the production and / or packaging of product
  • Assist daily production in operating and monitoring technical, computerized, production machinery, ensuring quality standards are maintained
  • Assumes other duties and responsibilities, as necessary, within the Unit Dose / Multi Dose department, in an effort to provide the required support to ensure adherence to the production schedule
  • Incumbent has full authority to make decisions and/or take action that is required to carry out job duties
  • Internal requirements include compliance with ethics, environmental health and safety, financial, human resources, cGMP procedures, general business policies, requirements and objectives
  • The incumbent must be willing to take temporary assignments as required
  • Regulated Responsibilities (including cGMP and EHS)
  • Incumbent is expected to be fully compliant with all criteria established by governmental agencies, Ministry of Health, and legislative requirements including, but not limited to: the FDA, European Community (EC), ISO 13485 - Medical
  • Devices, European Economic Community Medical Device Directive (MDD), Canadian Medical Device Regulations (CMDR), OSHA, Sarbanes-Oxley, EPA, DOT, EEOC, and ADA
  • Incumbent will work to ensure that the company is in compliance with all environmental, health and safety requirements and assure our business practices enhance the welfare of our customers, employees and the community in which we operate.

Plastics Lead

Allergan
01.2015 - Current
  • Supervise team of 12
  • Make Sterile Fill Bottles, Caps and Tips
  • Minimized resource and time losses by addressing employee or production issue directly and implementing timely solutions.
  • Evaluated employee skills and knowledge regularly, training, and mentoring individuals with lagging skills.

Tank Line Supervisor

Behlen Country
01.2014 - 01.2015
  • Inspect finished products for quality and adherence to customer specifications
  • Set up and operate production equipment in accordance with current good manufacturing practices and standard operating procedures
  • Calibrate or adjust equipment to ensure quality production, using tools such as calipers, micrometers, height gauges, protractors, or ring gauges
  • Set up and verify the functionality of safety equipment
  • Troubleshoot problems with equipment, devices, or products
  • Monitor and adjust production processes or equipment for quality and productivity
  • Test products or subassemblies for functionality or quality
  • Start up and shut down processing equipment
  • Prepare and assemble materials
  • Provide advice or training to other technicians
  • Measure and record data associated with operating equipment
  • Keep production logs
  • Clean production equipment or work areas.

Education

Associate of Science -

McLennan Community College
2003

Skills

  • Forklift Certifications
  • Equipment Preparation
  • Methods of Production
  • Production and Processing Equipment Maintenance
  • Autoclave Cleaning and Sterilization
  • Grade A Gown Certified

Accomplishments

  • Skills
  • Quality Control Analysis Troubleshooting
  • Forklift Certification
  • Supervisory Experience
  • Production and Processing Equipment Maintenance

Timeline

Plastics Lead

Allergan
01.2015 - Current

Tank Line Supervisor

Behlen Country
01.2014 - 01.2015

Manufacturing Technician

Associate of Science -

McLennan Community College
Joe Dominguez