Automation Engineer

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    "description": "<p><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt;\">Quality Agents, LLC offers validation and quality expertise to the pharmaceutical and biotechnology industries. </span><br><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt;\">We are seeking a hands-on and detail-driven Automation Engineer to support the design, implementation, and maintenance of automation systems in a regulated biotech manufacturing environment. This role will play a key part in optimizing equipment performance, ensuring data integrity, and maintaining GMP compliance across automated systems.</span><br><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt;\">The ideal candidate has experience with PLCs, SCADA, building management systems (BMS), and process automation in GMP settings.</span></p>\n<p><br><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt; font-weight: bold;\">Key Responsibilities</span></p>\n<p><br><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt;\">•    Support automation projects related to manufacturing, utilities, and lab systems (e.g., bioreactors, chromatography skids, CIP/SIP systems).</span><br><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt;\">•    Develop, modify, and troubleshoot automation logic (PLC, SCADA, DCS) in support of process control and equipment integration.</span><br><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt;\">•    Work closely with cross-functional teams on system requirements, design specifications, and commissioning/qualification (IQ/OQ/PQ) activities.</span><br><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt;\">•    Maintain and update automation-related documentation including functional specs, FRS, URS, and validation protocols.</span><br><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt;\">•    Ensure compliance with 21 CFR Part 11, data integrity, GAMP5, and other relevant GMP regulations.</span><br><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt;\">•    Collaborate with QA, Validation, Engineering, and IT to support system lifecycle management and change control.</span><br><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt;\">•    Support deviation investigations, CAPAs, and root cause analysis for automation-related issues</span></p>\n<p><br><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt; font-weight: bold;\">Minimum Requirements:</span></p>\n<p><br><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt;\">•    B.S. in Electrical Engineering, Chemical Engineering, Computer Science, or a related field.</span><br><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt;\">•    3+ years of experience in automation engineering within a biotech, pharmaceutical, or GMP-regulated environment.</span><br><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt;\">•    Experience with automation platforms such as Allen-Bradley, Siemens, DeltaV, Rockwell, Wonderware/AVEVA, or similar.</span><br><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt;\">•    Strong understanding of control systems, instrumentation, and network infrastructure in GMP settings.</span><br><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt;\">•    Familiarity with automation validation and documentation standards.</span></p>\n<p><br><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt; font-weight: bold;\">Quality Agents offers a full suite of benefits for full-time employees including:</span></p>\n<p><br><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt;\">•    Health, dental and vision insurance</span><br><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt;\">•    Life, AD&amp;D and Disability Insurance</span><br><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt;\">•    Health savings account for participants in our health plan</span><br><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt;\">•    401k retirement plan</span><br><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt;\">•    Paid time off</span><br><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt;\">•    Paid holidays</span></p>\n<p><br><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt;\">Quality Agents accepts applications on an on-going basis in order to build a talent pool of potential candidates. These applications remain open for consideration, as positions become available, for one (1) year from the date of application. After that time, or if your application information changes, please submit your application again.</span></p>",
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