JT393 - SPECIALIST MANUFACTURING

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    "description_html": "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 to a world-class manufacturing industry in Puerto Rico & USA.<br><br>Responsibilities:<ul><li><strong>Support the execution of manufacturing/quality systems such as non-conformances, process validation, procedures, training, and new product introductions.</strong></li><li>Apply process, operational, scientific expertise, basic compliance knowledge, and analytical and troubleshooting skills to support manufacturing operations.</li><li>May serve as primary production process owner for process support systems and assist with process ownership responsibilities on more complex process systems.</li><li><strong>Own change controls for manufacturing process changes</strong></li><li>Support major/trend deviation investigations throughout the whole lifecycle including Root Cause Analysis investigation, determination of Corrective/Preventive Actions, authoring process investigation reports, and presenting within regulatory inspections.</li><li>Support Risk Assessments exercises and Microbial assessment evaluations.</li><li>Led commercial campaign readiness and effectively communicate and collaborate with cross function areas.</li><li>Assist in the generation of training materials and assist in providing training on scientific or technical aspects of the process.</li><li>Provide commercial support when needed and assist on the floor troubleshooting.</li><li>Design, coordinate, and support execution of functional tests, water tests, and other runs to challenge process and operations during major changes, or campaign readiness. Generate technical protocols as needed.</li><li>Assist and provide guidance during MBR (Master Batch Record) creation/revisions.</li><li>Perform assessment to support process, automation, or equipment modification or implementation of special projects</li><li>Initiate, revise, and approve standard manufacturing procedures. Ensure all procedures reflect current operations. Serve as a document owner.</li><li>Assess process performance and review of performance data. Evaluate, plan, and implement solutions for process improvement opportunities.</li><li>Complete assessments for CAPA applicability requests from other plants/sites</li><li>Complete assessment for new or changes in BOM's (Bill of Materials)</li><li>Serves as a peer-recognized specialist in at least one area, with overall responsibility for determining methodologies in that area.<br> </li></ul><br>Qualifications:<ul><li><strong>Educational background in Life Sciences and/or Engineering.</strong></li><li><strong>In-depth experience of bio-processing unit operations</strong></li><li>Knowledge in Root Cause Analysis methodologies (Fishbone, Six Boxes, Fishbone, 5 Why’s, Kepner Tregoe)</li><li>Familiar with Lean Manufacturing Practices</li><li>Ability to communicate and collaborate with technical and management staff within manufacturing, process development, and quality.</li><li>Proficiency in GDP (Good Documentation Practices) on a regulated environment</li><li><strong>Knowledge in systems: Trackwise, Spotfire, CDOCS, and process monitoring platforms</strong></li><li>Strong Technical Writing/presentation abilities, and excellent written/verbal communication skills in</li><li>English and Spanish</li><li>Skilled in performance of GMP production operations</li><li>Regulatory knowledge and interactions.</li><li>Participate and help lead cross-functional teams.</li><li><strong>8-hour shift, Mon-Fri 8am-5pm (flexibility for on-call support at any time)</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 to a world-class manufacturing industry in Puerto Rico & USA.\nResponsibilities: Support the execution of manufacturing/quality systems such as non-conformances, process validation, procedures, training, and new product introductions.\n Apply process, operational, scientific expertise, basic compliance knowledge, and analytical and troubleshooting skills to support manufacturing operations.\n May serve as primary production process owner for process support systems and assist with process ownership responsibilities on more complex process systems.\n Own change controls for manufacturing process changes\n Support major/trend deviation investigations throughout the whole lifecycle including Root Cause Analysis investigation, determination of Corrective/Preventive Actions, authoring process investigation reports, and presenting within regulatory inspections.\n Support Risk Assessments exercises and Microbial assessment evaluations.\n Led commercial campaign readiness and effectively communicate and collaborate with cross function areas.\n Assist in the generation of training materials and assist in providing training on scientific or technical aspects of the process.\n Provide commercial support when needed and assist on the floor troubleshooting.\n Design, coordinate, and support execution of functional tests, water tests, and other runs to challenge process and operations during major changes, or campaign readiness. Generate technical protocols as needed.\n Assist and provide guidance during MBR (Master Batch Record) creation/revisions.\n Perform assessment to support process, automation, or equipment modification or implementation of special projects\n Initiate, revise, and approve standard manufacturing procedures. Ensure all procedures reflect current operations. Serve as a document owner.\n Assess process performance and review of performance data. Evaluate, plan, and implement solutions for process improvement opportunities.\n Complete assessments for CAPA applicability requests from other plants/sites\n Complete assessment for new or changes in BOM's (Bill of Materials)\n Serves as a peer-recognized specialist in at least one area, with overall responsibility for determining methodologies in that area.\nQualifications: Educational background in Life Sciences and/or Engineering.\n In-depth experience of bio-processing unit operations\n Knowledge in Root Cause Analysis methodologies (Fishbone, Six Boxes, Fishbone, 5 Why’s, Kepner Tregoe)\n Familiar with Lean Manufacturing Practices\n Ability to communicate and collaborate with technical and management staff within manufacturing, process development, and quality.\n Proficiency in GDP (Good Documentation Practices) on a regulated environment\n Knowledge in systems: Trackwise, Spotfire, CDOCS, and process monitoring platforms\n Strong Technical Writing/presentation abilities, and excellent written/verbal communication skills in\n English and Spanish\n Skilled in performance of GMP production operations\n Regulatory knowledge and interactions.\n Participate and help lead cross-functional teams.\n 8-hour shift, Mon-Fri 8am-5pm (flexibility for on-call support at any time)\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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      "datePosted": "2026-05-27",
      "description": "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 to a world-class manufacturing industry in Puerto Rico & USA.<br><br>Responsibilities:<ul><li><strong>Support the execution of manufacturing/quality systems such as non-conformances, process validation, procedures, training, and new product introductions.</strong></li><li>Apply process, operational, scientific expertise, basic compliance knowledge, and analytical and troubleshooting skills to support manufacturing operations.</li><li>May serve as primary production process owner for process support systems and assist with process ownership responsibilities on more complex process systems.</li><li><strong>Own change controls for manufacturing process changes</strong></li><li>Support major/trend deviation investigations throughout the whole lifecycle including Root Cause Analysis investigation, determination of Corrective/Preventive Actions, authoring process investigation reports, and presenting within regulatory inspections.</li><li>Support Risk Assessments exercises and Microbial assessment evaluations.</li><li>Led commercial campaign readiness and effectively communicate and collaborate with cross function areas.</li><li>Assist in the generation of training materials and assist in providing training on scientific or technical aspects of the process.</li><li>Provide commercial support when needed and assist on the floor troubleshooting.</li><li>Design, coordinate, and support execution of functional tests, water tests, and other runs to challenge process and operations during major changes, or campaign readiness. Generate technical protocols as needed.</li><li>Assist and provide guidance during MBR (Master Batch Record) creation/revisions.</li><li>Perform assessment to support process, automation, or equipment modification or implementation of special projects</li><li>Initiate, revise, and approve standard manufacturing procedures. Ensure all procedures reflect current operations. Serve as a document owner.</li><li>Assess process performance and review of performance data. Evaluate, plan, and implement solutions for process improvement opportunities.</li><li>Complete assessments for CAPA applicability requests from other plants/sites</li><li>Complete assessment for new or changes in BOM's (Bill of Materials)</li><li>Serves as a peer-recognized specialist in at least one area, with overall responsibility for determining methodologies in that area.<br> </li></ul><br>Qualifications:<ul><li><strong>Educational background in Life Sciences and/or Engineering.</strong></li><li><strong>In-depth experience of bio-processing unit operations</strong></li><li>Knowledge in Root Cause Analysis methodologies (Fishbone, Six Boxes, Fishbone, 5 Why’s, Kepner Tregoe)</li><li>Familiar with Lean Manufacturing Practices</li><li>Ability to communicate and collaborate with technical and management staff within manufacturing, process development, and quality.</li><li>Proficiency in GDP (Good Documentation Practices) on a regulated environment</li><li><strong>Knowledge in systems: Trackwise, Spotfire, CDOCS, and process monitoring platforms</strong></li><li>Strong Technical Writing/presentation abilities, and excellent written/verbal communication skills in</li><li>English and Spanish</li><li>Skilled in performance of GMP production operations</li><li>Regulatory knowledge and interactions.</li><li>Participate and help lead cross-functional teams.</li><li><strong>8-hour shift, Mon-Fri 8am-5pm (flexibility for on-call support at any time)</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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