Quality Manufacturing Technician at Engineering Resource Group

Description

• Permanent position for a Quality Manufacturing Technician to treat medical device surfaces by applying complex wet chemistry.
• Utilize aseptic techniques in a small scale production, and conduct in process and final QC testing.
• Follow standard operating procedures (SOPs), work instructions, and cleaning and EHS guidelines.
• Perform assays to test the efficacy of antimicrobial surfaces using FTIR, chromatography and other specialized equipment.
• Accurately record and interpret assay results production Batch Records, and escalate and document any deviations.
• Analyze data using scientific and statistical techniques and prepare reports summarizing findings and insights.
• Collaborate with R&D, Biology and Microbiology scientists in company meeting forums.
• Maintain process control and take initiatives with continuous improvement.
• Manage inventory of raw materials, supplies, reagents, consumables including ordering from suppliers.
• Report equipment issues, manage calibrations and preventative maintenance using 3rd party.
• Properly dispose of wastes.

Requirements

• Associate Degree preferred
• Minimum 2 years of wet chemistry laboratory experience.
• Experience with GMP and controlled manufacturing processes and basic training in Quality Control.
• Problem solving, time management, analytical, and communication skills.
• Familiarity with MS Office, basic laboratory mathematics, Excel and Minitab to analyze data using scientific and statistical methods.
• Excellent attention to detail to ensure accuracy and reliability of experimental results.
• Ability to maintain an organized lab notebook.
• Experience with and general understanding of ISO and 21CFR.

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