Receiving Technician - S4

<h3> </h3><h3><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><strong>Purpose Statement</strong></span></h3><p> </p><p><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">The Receiving Technician is responsible for providing an independent and unbiased evaluation of incoming materials to ensure they meet quality specifications and regulatory requirements before being released for production. This role supports supplier quality by conducting inspections, managing non-conforming materials, maintaining quality documentation, and contributing to continuous quality improvement.</span></p><h3> </h3><h3><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><strong>Minimum Requirements</strong></span></h3><p> </p><ul data-spread="false"><li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Diploma in Engineering, Science, Biomedical, Quality, or a related field.</span></li><li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Minimum 4 years of experience in Incoming Quality Control (IQC), Receiving Inspection, or a manufacturing/medical device environment.</span></li></ul><h3> </h3><h3><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><strong>Key Responsibilities</strong></span></h3><p> </p><ul data-spread="false"><li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Perform incoming inspection of raw materials, components, and purchased parts using approved inspection methods and measuring equipment.</span></li><li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Verify inspection results and ensure materials comply with drawings, specifications, and quality standards.</span></li><li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Identify, document, and investigate non-conforming materials, and support root cause analysis and CAPA activities.</span></li><li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Maintain accurate inspection records and QA documentation in accordance with company procedures.</span></li><li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Support supplier quality activities, audits, material qualifications, and continuous improvement initiatives.</span></li><li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Handle discrepant materials according to established procedures and maintain quarantine/MRB inventory when required.</span></li><li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Ensure compliance with GMP, ISO 13485, FDA Quality System Regulations, and Good Documentation Practices (GDP).</span></li><li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Provide technical support and guidance on incoming inspection processes as required.</span></li></ul><h3> </h3><h3><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><strong>Required Skills & Knowledge</strong></span></h3><p> </p><ul data-spread="false"><li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Proficient in using inspection and measurement equipment such as <strong>Smartscope, Instron, calipers, micrometers, gauges</strong>, and other precision measuring instruments.</span></li><li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Strong understanding of <strong>Incoming Quality Control (IQC)</strong> processes.</span></li><li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Knowledge of <strong>GMP, ISO 13485, FDA 21 CFR Part 820, Good Documentation Practices (GDP), CAPA, Non-Conformance processes, Sampling Plans, and AQL methodologies</strong>.</span></li><li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Strong problem-solving and root cause analysis skills.</span></li><li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Able to work independently with minimal supervision.</span></li><li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Good communication, documentation, and report-writing skills.</span></li><li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Experience in the medical device manufacturing industry is highly preferred.</span></li></ul><p> </p><p> </p><p>About Us</p><p>As a global medical technology leader for more than 45 years, our mission at Boston Scientific (NYSE: BSX) is to transform lives through innovative medical solutions that improve the health of patients.

If you’re looking to truly make a difference to people both around the world and around the corner, there’s no better place to make it happen.</p>