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production chemist resume example with 20+ years of experience

Jessica Claire
, , 609 Johnson Ave., 49204, Tulsa, OK 100 Montgomery St. 10th Floor
Home: (555) 432-1000 - Cell: - resumesample@example.com - : - -
Summary

Experienced in the manufacturing area of medical devices, Production Chemist with over 12 years of experience working in a laboratory setting. Skilled in wet lab chemistry and quality control processes to improve products. Excellent communicator with demonstrated talents in planning, organizing and critical thinking. Looking for a new position where expertise my experience in the manufacturing area of medical devices can be utilized.

Skills
  • Friendly, Positive Attitude
  • Reliable & Trustworthy
  • Costing Support
  • Calibration Skills
  • Wet Chemistry
  • Chemical Handling
  • Good Work Ethic
  • Computer Skills
  • Planning & Organizing
  • Critical Thinking
  • Fluent in Spanish
  • Quality Control
Experience
10/2010 to Current
Production Chemist Abbott Laboratories Bronson, MI,
  • Monitored packaging and storage of hazardous materials and waste to comply with laboratory, state and federal safety regulations.
  • Organized and cleaned laboratory equipment to adhere to cGMP standards.
  • Made decisions and executed changes based on process data, quality checks and test results to keep products at target and within specifications. Continuously monitored the safety practices in the lab, keeping the team compliant with standards.
  • Calibrated and validated laboratory equipment and instrumentation according to manufacturer recommendations. Maintained laboratory instruments, including calibration and troubleshooting.
  • Ordered supplies, inventoried chemicals and materials and summarized and recorded data to meet control and research requirements.
  • Organized, analyzed and prepared data reports in compliance with operations and record-keeping standards.
  • Worked successfully with diverse group of coworkers to accomplish goals and address issues related to our products and services.
  • Purchased chemicals and other supplies to meet needs of upcoming laboratory work.
  • Managed data and documentation, including filing, naming and data backup. Perform data-entry of received work orders to accurately reflect inventory levels.
  • Work under FDA/QSR guidelines
  • Operate laboratory equipment
  • Generate, issue, and control, all work orders, and batch records.
  • Coordinate the prioritizing and expediting of work orders, to include schedule changes.
  • Prepare batch records and initiate work orders, and entry data as need it to runs the Lab schedule.
  • Reviews all documentation for adherence to GMP, ISO, FDA, and SOP compliance.
  • Assist the manufacturing department management with other activities such as ordering raw materials, office supplies, batch records.
  • Performs Cycle counts monthly to assist physical inventory.
  • Collect and record performance data, production data, and other related data.
  • Prepare Lab schedule and spreadsheets
06/2008 to 10/2010
Manufacturing Operator Solvay Pharma Houston, TX,
  • Knowledge of ESD, and cGMP guidelines
  • Responsible for quality control of workmanship.
  • Assist the engineers run protocols for the software validation project for the Amigo Pump.
  • Work with printed circuit boards (PCB) and Main Board programming experience.
  • Familiarity with Hand soldering.
  • Assembly of components in the area of Sub-Assembly using small hands tools.
  • Working the Ultrasonic (US) welder and Ultraviolet (UV) curing system.
  • Ability to complete work orders in an accurate and timely manner.
  • Capability to focus on quality control and accuracy.
  • Work with minimum amount of supervision.
  • Reduced health and safety risks with strict adherence to safety protocols and PPE requirements.
  • Hand-assembled needed parts with bolts and screws.
  • Detected work-piece defects and machine malfunctions, maintaining apparatus to prevent future issues.
03/2000 to 05/2008
Manufacturing Associate I Carlisle Interconnect Technologies San Diego, CA,
  • Ability to operate Industrial Inspection Microscope, Smart Scope MVP, Toolmaker, and Wind Coils machine.
  • Knowledge of and experience with Microsoft Office software for data entry and retrieval
  • Update and maintain customer data.
  • Daily report of yields.
  • Familiar with general office equipment.
  • Productive and efficient work habits without supervision
  • Managed the CNV mandrel inventory.
  • Filled purchase requisition forms for sign approval.
  • Contact vendors and request quote prices.
  • Issuing material to production floor as needed.
  • Prepared weekly inventory reports.
  • Performed monthly Safety Audits as a member of the CNV Safety Team.
  • Attend monthly meetings to discuss safety issues and write reports.
Education and Training
Expected in 12/1994 to to
Associate of Science: Computer
Universidad Autonoma - Nicaragua,
GPA:
Expected in to to
: English Language And Literature
Miami Dade College - Miami, FL
GPA:
Languages
Spanish:
Native/ Bilingual
Negotiated:
Accomplishments
  • Work closely with engineers in the Material Characterization project measuring materials and data entry using sophisticated equipment which resulted in yield improvements on the Microcatheters area,
Certifications
  • DOT Training
  • RCRA-Hazardous Waste
  • Hazardous Chemical Waste

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Resume Overview

School Attended

  • Universidad Autonoma
  • Miami Dade College

Job Titles Held:

  • Production Chemist
  • Manufacturing Operator
  • Manufacturing Associate I

Degrees

  • Associate of Science
  • Some College (No Degree)

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