JT420 - MANUFACTURING PROCESS TECHNICIAN NS

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    "heading": "JT420 - MANUFACTURING PROCESS TECHNICIAN NS",
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    "description_html": "<p>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.</p><p>Responsibilities:</p><ul><li><strong>Operate automated and innovative manufacturing equipment for our products' packaging operations.</strong></li><li>This individual will be trained and cross-trained to both operate and troubleshoot issues (in the event of faults and machine stops) across a variety of equipment such as: automated, assembly, labeling, printing, and robotic automation.</li><li><strong>The technician will ensure product quality by monitoring the performance of the equipment and will utilize their mechanical proficiency to conduct machine troubleshooting and problem-solving skills in a fast-paced manufacturing environment.</strong></li><li>Under limited supervision, perform equipment setup, operation, troubleshoot to meet all standards for safety, quality and efficiency.<br>Maintain machine uptime, perform any fault clearing and clear stoppages on automated equipment.</li><li>Perform basic, routine manufacturing process operations such as dispensing of raw materials, material reconciliation, line clearance, basic analytics, and record transactions</li><li>Assist in the review of documentation for assigned areas (i.e. procedures, job plans, logs, area audits and batch records)</li><li>Assist as training resource on manufacturing tasks and equipment use</li><li>Use human machine interfaces (HMIs) to identify alarms and correct line stoppages.</li><li>Ensures components and products are available for a continuous operation.</li><li>Carries out equipment inspections and generates emergency, corrective, or preventative work orders.</li><li>Troubleshoot and identify potential solutions for mechanical errors, safety issues or general operating inefficiencies within the production processes.</li></ul><br>Qualifications: <ul><li>Associate degree (preferred)</li><li><strong>1-3 year of experience</strong> in working experience in GMP, Medical Device, or Biotech Manufacturing regulated environment.</li><li>Experience in a drug product manufacturing environment.<br>Ability to assemble, disassemble, operate and understand simple to moderately complex equipment per procedures.</li><li>Able to use computer systems to support material inventory system (SAP transactions) and electronic batch records.</li><li>Safely follow standardized operating procedures including material handling, record keeping, assembly and packaging. Must follow Good Manufacturing Practices (GMPs).</li><li>Reports to Team Leader or Production Supervisor of any discrepancies to ensure quality standards and safety of operations are always maintained.</li><li>Train fellow staff on the manufacturing processes, equipment, and general</li><li><strong>Available to support Operation in Non-Standard shift that includes weekends and /or holidays as determined by business skills.</strong></li><li><strong>12 hour night shifts 6pm-6:30am</strong></li></ul><p><span style=\\\"font-size:10px\\\"><em>Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.</em></span></p>",
    "description_text": "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.\n Responsibilities:\n Operate automated and innovative manufacturing equipment for our products' packaging operations.\n This individual will be trained and cross-trained to both operate and troubleshoot issues (in the event of faults and machine stops) across a variety of equipment such as: automated, assembly, labeling, printing, and robotic automation.\n The technician will ensure product quality by monitoring the performance of the equipment and will utilize their mechanical proficiency to conduct machine troubleshooting and problem-solving skills in a fast-paced manufacturing environment.\n Under limited supervision, perform equipment setup, operation, troubleshoot to meet all standards for safety, quality and efficiency.\nMaintain machine uptime, perform any fault clearing and clear stoppages on automated equipment.\n Perform basic, routine manufacturing process operations such as dispensing of raw materials, material reconciliation, line clearance, basic analytics, and record transactions\n Assist in the review of documentation for assigned areas (i.e. procedures, job plans, logs, area audits and batch records)\n Assist as training resource on manufacturing tasks and equipment use\n Use human machine interfaces (HMIs) to identify alarms and correct line stoppages.\n Ensures components and products are available for a continuous operation.\n Carries out equipment inspections and generates emergency, corrective, or preventative work orders.\n Troubleshoot and identify potential solutions for mechanical errors, safety issues or general operating inefficiencies within the production processes.\nQualifications:  Associate degree (preferred)\n 1-3 year of experience in working experience in GMP, Medical Device, or Biotech Manufacturing regulated environment.\n Experience in a drug product manufacturing environment.\nAbility to assemble, disassemble, operate and understand simple to moderately complex equipment per procedures.\n Able to use computer systems to support material inventory system (SAP transactions) and electronic batch records.\n Safely follow standardized operating procedures including material handling, record keeping, assembly and packaging. Must follow Good Manufacturing Practices (GMPs).\n Reports to Team Leader or Production Supervisor of any discrepancies to ensure quality standards and safety of operations are always maintained.\n Train fellow staff on the manufacturing processes, equipment, and general\n Available to support Operation in Non-Standard shift that includes weekends and /or holidays as determined by business skills.\n 12 hour night shifts 6pm-6:30am\n Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.",
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      "title": "JT420 - MANUFACTURING PROCESS TECHNICIAN NS",
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      "datePosted": "2026-05-20",
      "description": "<p>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.</p><p>Responsibilities:</p><ul><li><strong>Operate automated and innovative manufacturing equipment for our products' packaging operations.</strong></li><li>This individual will be trained and cross-trained to both operate and troubleshoot issues (in the event of faults and machine stops) across a variety of equipment such as: automated, assembly, labeling, printing, and robotic automation.</li><li><strong>The technician will ensure product quality by monitoring the performance of the equipment and will utilize their mechanical proficiency to conduct machine troubleshooting and problem-solving skills in a fast-paced manufacturing environment.</strong></li><li>Under limited supervision, perform equipment setup, operation, troubleshoot to meet all standards for safety, quality and efficiency.<br>Maintain machine uptime, perform any fault clearing and clear stoppages on automated equipment.</li><li>Perform basic, routine manufacturing process operations such as dispensing of raw materials, material reconciliation, line clearance, basic analytics, and record transactions</li><li>Assist in the review of documentation for assigned areas (i.e. procedures, job plans, logs, area audits and batch records)</li><li>Assist as training resource on manufacturing tasks and equipment use</li><li>Use human machine interfaces (HMIs) to identify alarms and correct line stoppages.</li><li>Ensures components and products are available for a continuous operation.</li><li>Carries out equipment inspections and generates emergency, corrective, or preventative work orders.</li><li>Troubleshoot and identify potential solutions for mechanical errors, safety issues or general operating inefficiencies within the production processes.</li></ul><br>Qualifications: <ul><li>Associate degree (preferred)</li><li><strong>1-3 year of experience</strong> in working experience in GMP, Medical Device, or Biotech Manufacturing regulated environment.</li><li>Experience in a drug product manufacturing environment.<br>Ability to assemble, disassemble, operate and understand simple to moderately complex equipment per procedures.</li><li>Able to use computer systems to support material inventory system (SAP transactions) and electronic batch records.</li><li>Safely follow standardized operating procedures including material handling, record keeping, assembly and packaging. Must follow Good Manufacturing Practices (GMPs).</li><li>Reports to Team Leader or Production Supervisor of any discrepancies to ensure quality standards and safety of operations are always maintained.</li><li>Train fellow staff on the manufacturing processes, equipment, and general</li><li><strong>Available to support Operation in Non-Standard shift that includes weekends and /or holidays as determined by business skills.</strong></li><li><strong>12 hour night shifts 6pm-6:30am</strong></li></ul><p><span style=\\\"font-size:10px\\\"><em>Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.</em></span></p>",
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