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JT691 - ASSOCIATE MANUFACTURING PROCESS TECHNICIAN na Quality Consulting Group

Quality Consulting Group · New Albany, Estados Unidos Da América · Onsite

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QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.

Responsibilities:
  • Load components and materials into packaging equipment.
  • Operating a variety of packaging equipment (Assembly, labeler, cartoner, case packer, autoinjector testing, ID testing)
  • Maintaining strict adherence to SOP and cGMP requirements and expectations
  • Assist in troubleshooting equipment and system errors as needed (or escalate to management).
  • Routinely perform moderately-complex to complex processes according to Standard Operating Procedure (SOP).
  • Specific responsibilities include inspection and packaging of product-filled vials per procedures and batch records.  
  • Routine maintenance and cleaning of equipment
  • Assisting or participating in other manufacturing operations (e.g., filling support activities)
  • Internal support operations (e.g. stocking items, tracking inventory, material movement)
  • Recognizing and reporting malfunctions and making necessary adjustments to equipment. 
  • Training new MPTs on routine tasks.
  • Reconcile components and products and calculate product exposure to room temperature.

Qualifications: 
  • High school/GED + 1 year of work or military experience or Associate degree
  • Required to know, comprehend, and apply packaging configurations, as well as understand, follow and document batch records for the inspection and packaging process.
  • Tech Savy and have good attendance record is required.
  • Pharma experience is preferred but not required.
  • Has a track record of being fluent in technology (navigating computer systems and software beyond just Microsoft products) and using those skills in a fast-paced manner.
  • Prior experience in cGMP environments.
  • Filling and finishing manufacturing experience, preferably vial inspection
  • Understanding of measurements, calculations and the metric system
  • Candidate must be willing to work with 12 hours rotational shift with breaks. 6AM - 6:30PM
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