JT369 - MICROBIOLOGIST STERILIZ I

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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 in a world-class manufacturing industry in Puerto Rico & USA.<br><br>Responsibilities: <ul><li><strong>Analyzes chemical, biological or microbiological products, raw materials, in-process materials, release test samples or stability samples in support of the company's quality program.</strong></li><li>Prepares, cleans, disinfects, and/or sterilizes instruments, materials, products, and/or supplies.</li><li><strong>Follows protocols and regulations in order to clean, store, and/or deliver products, supplies, and/or instruments.</strong></li><li>Interprets and evaluates the analyses in terms of accuracy and precision compared against established specifications and <strong>recommends and implements corrective action where necessary.</strong></li><li>Develops, validates, and implements controlled environment methods.</li><li>Applies existing techniques and procedures with recommendations and implementation of modification for improved efficiency, or devises and develops new analytical methods and techniques.</li><li><strong>Performs qualitative tests or quantitative assays on samples using techniques that vary from use of standard analytical equipment to highly modern and automated instrumentation.</strong></li><li>May also be involved in establishing requirements for the transfer of methodology from R&D.</li></ul><br>Qualifications:<ul><li>Bachelor’s degree in <strong>Science (Microbiology or Biology preferred).</strong></li><li><strong>2-3 years of relevant experience.</strong></li><li><strong>Experience Non-Conformance investigations and Sterility Assessment.</strong></li><li><strong>Experience in b</strong><strong>acterial endotoxins analysis,</strong> <strong>Bioburden and Environmental.   </strong></li><li><strong>Environmental Validation experience.</strong></li><li><strong>Microbiology and sterilization knowledge (e.g. EO Sterilization experience).</strong></li><li>Bilingual</li><li>Working Shift: <strong>1pm to10pm- Tuesday to Saturday.</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.\nResponsibilities:  Analyzes chemical, biological or microbiological products, raw materials, in-process materials, release test samples or stability samples in support of the company's quality program.\n Prepares, cleans, disinfects, and/or sterilizes instruments, materials, products, and/or supplies.\n Follows protocols and regulations in order to clean, store, and/or deliver products, supplies, and/or instruments.\n Interprets and evaluates the analyses in terms of accuracy and precision compared against established specifications and recommends and implements corrective action where necessary.\n Develops, validates, and implements controlled environment methods.\n Applies existing techniques and procedures with recommendations and implementation of modification for improved efficiency, or devises and develops new analytical methods and techniques.\n Performs qualitative tests or quantitative assays on samples using techniques that vary from use of standard analytical equipment to highly modern and automated instrumentation.\n May also be involved in establishing requirements for the transfer of methodology from R&D.\nQualifications: Bachelor’s degree in Science (Microbiology or Biology preferred).\n 2-3 years of relevant experience.\n Experience Non-Conformance investigations and Sterility Assessment.\n Experience in b acterial endotoxins analysis,   Bioburden and Environmental.\n Environmental Validation experience.\n Microbiology and sterilization knowledge (e.g. EO Sterilization experience).\n Bilingual\n Working Shift: 1pm to10pm- Tuesday to Saturday.\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": "2026-05-22",
      "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 in a world-class manufacturing industry in Puerto Rico & USA.<br><br>Responsibilities: <ul><li><strong>Analyzes chemical, biological or microbiological products, raw materials, in-process materials, release test samples or stability samples in support of the company's quality program.</strong></li><li>Prepares, cleans, disinfects, and/or sterilizes instruments, materials, products, and/or supplies.</li><li><strong>Follows protocols and regulations in order to clean, store, and/or deliver products, supplies, and/or instruments.</strong></li><li>Interprets and evaluates the analyses in terms of accuracy and precision compared against established specifications and <strong>recommends and implements corrective action where necessary.</strong></li><li>Develops, validates, and implements controlled environment methods.</li><li>Applies existing techniques and procedures with recommendations and implementation of modification for improved efficiency, or devises and develops new analytical methods and techniques.</li><li><strong>Performs qualitative tests or quantitative assays on samples using techniques that vary from use of standard analytical equipment to highly modern and automated instrumentation.</strong></li><li>May also be involved in establishing requirements for the transfer of methodology from R&D.</li></ul><br>Qualifications:<ul><li>Bachelor’s degree in <strong>Science (Microbiology or Biology preferred).</strong></li><li><strong>2-3 years of relevant experience.</strong></li><li><strong>Experience Non-Conformance investigations and Sterility Assessment.</strong></li><li><strong>Experience in b</strong><strong>acterial endotoxins analysis,</strong> <strong>Bioburden and Environmental.   </strong></li><li><strong>Environmental Validation experience.</strong></li><li><strong>Microbiology and sterilization knowledge (e.g. EO Sterilization experience).</strong></li><li>Bilingual</li><li>Working Shift: <strong>1pm to10pm- Tuesday to Saturday.</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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