Process Equipment Engineer

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    "description_html": "<p>&nbsp;<strong>Greetings from Kashiv Biosciences!!!</strong></p><p><br>We are looking for <strong>Process Equipment Engineer</strong> for our <strong>Biosimilar Manufacturing Plant</strong> Based out of <strong>Ahmedabad</strong>. Below are the further details.<br><br><u><strong>Roles &amp; Responsibilities</strong></u> <br></p><ul><li>Responsible for the Plant Maintenance activity of <strong>DS (Drug Substance)</strong> section equipment's such as <strong>Fermenters, Process vessels, CIP vessels, batch centrifuges, TFF systems, Merck chromatography columns, Filter press</strong>.&nbsp;</li><li>Responsible for Maintaining of biologics <strong>MFG units (Cell Culture), Filling Facility (DP),QC,WH and R&amp;D facility .&nbsp;</strong></li><li>Maintenance of <strong>Biologics manufacturing facility (Mammalian)</strong> including Development and QC lab(Microbiology).</li><li>Responsible for <strong>QMS Documentation, validation and new Equipment Qualification</strong>.</li></ul><p><u><strong>Required Instruments Exposure:</strong></u></p><ul><li>Bioreactor&nbsp;</li><li>Fermenter</li><li>Media, Buffer &amp; CIP vessel</li><li>Continuous Centrifuge&nbsp;</li><li>Continues Kill system&nbsp;</li><li>Homogenizer&nbsp;</li><li>Chrome system&nbsp;</li><li>TFF system</li><li>Autoclave&nbsp;</li><li>Chromatography</li></ul><p><br></p><p>Interested candidate please share the resume on my mail id <strong>[email protected]</strong>&nbsp;</p>",
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      "description": "<p>Description</p><p> <strong>Greetings from Kashiv Biosciences!!!</strong></p><p><br/>We are looking for <strong>Process Equipment Engineer</strong> for our <strong>Biosimilar Manufacturing Plant</strong> Based out of <strong>Ahmedabad</strong>. Below are the further details.<br/><br/><u><strong>Roles & Responsibilities</strong></u> <br/></p><ul><li>Responsible for the Plant Maintenance activity of <strong>DS (Drug Substance)</strong> section equipment's such as <strong>Fermenters, Process vessels, CIP vessels, batch centrifuges, TFF systems, Merck chromatography columns, Filter press</strong>. </li><li>Responsible for Maintaining of biologics <strong>MFG units (Cell Culture), Filling Facility (DP),QC,WH and R&D facility . </strong></li><li>Maintenance of <strong>Biologics manufacturing facility (Mammalian)</strong> including Development and QC lab(Microbiology).</li><li>Responsible for <strong>QMS Documentation, validation and new Equipment Qualification</strong>.</li></ul><p><u><strong>Required Instruments Exposure:</strong></u></p><ul><li>Bioreactor </li><li>Fermenter</li><li>Media, Buffer & CIP vessel</li><li>Continuous Centrifuge </li><li>Continues Kill system </li><li>Homogenizer </li><li>Chrome system </li><li>TFF system</li><li>Autoclave </li><li>Chromatography</li></ul><p><br/></p><p>Interested candidate please share the resume on my mail id <strong>[email protected]</strong> </p><p>Requirements</p><p><br/></p><p><br/></p><p> <u><strong>Candidate Details: </strong></u></p><ul><li><strong>Experience 08- 12 Years of Process Equipment Maintenance in Drug Substance Facility</strong></li><li><strong>Education:</strong> <strong>B.E/ B. Tech(Mechanical/ Electrical/ Electronics/ Instrumentation)</strong></li><li><strong>The candidate should be from Biopharma industry having exposure Drug Substance and Drug product Maintenance.</strong></li><li>The candidate should have exposure to regulatory Audits. </li><li>The candidate should be aware of <strong>GDP/ GMP Process</strong>.</li><li>The candidate should have exposure to <strong>new</strong> <strong>equipment qualification & QMS as well</strong>.</li><li>The candidate should have good communication skills.</li></ul>",
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    "requirements_text": "Candidate Details:\n Experience 08- 12 Years of Process Equipment Maintenance in Drug Substance Facility\n Education: B.E/ B. Tech(Mechanical/ Electrical/ Electronics/ Instrumentation)\n The candidate should be from Biopharma industry having exposure Drug Substance and Drug product Maintenance.\n The candidate should have exposure to regulatory Audits.\n The candidate should be aware of GDP/ GMP Process .\n The candidate should have exposure to new equipment qualification & QMS as well .\n The candidate should have good communication skills."
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