Quality Control Inspector Lead (Production)-QCIP

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    "description": "<p style=\"text-align:justify\">This position will support 2nd shift form 10am-8pm.</p>\n\n<p style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\"><strong>Position Summary: </strong>Under supervision of the Quality Control Supervisor, the Quality Control Inspector Lead Production (QCIP) is responsible for assuring that all products produced at Swiss American Products conforms to all regulatory and quality specifications. The QCIP is also responsible for providing job assignments for his/her shift as well as reporting any quality related issues to his/her supervisor. </span></p>\n\n<p style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\"><strong>Essential Duties and Responsibilities </strong></span></p>\n\n<ul>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Perform pre-production line inspections to ensure that all manufacturing lines are clear of materials from previous runs and is acceptable for use. </span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Provide line assignments to all QC inspectors on his/her shift. </span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Complete routine production line checks to check and accurately document finished good product for fill weights, visual conformity, and/or seal inspection</span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Collect, document and prepare samples for shipment for microbial and chemical testing.</span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Ensure that all operations in production areas are performed in accordance with SAP SOP&rsquo;s and FDA/GMP guidelines. </span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Assist in execution of product/process validation activities. </span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Collect and analyze appropriate samples for the release testing of finished goods and bulk products (i.e. pH and Viscosity).</span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Monitor all activity on the production floor to assure adherence to SAP SOP&rsquo;s and applicable FDA/GMP regulations. </span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Participate in investigations for process deviations and product quality failures and assist in implementation of corrective actions. </span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Provide a daily shift summary of production activities and any issues that may contribute to the manufacture of non-conforming products. </span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Conduct final review of MBR&rsquo;s priority to submitting to document control for review to ensure that each record is completely and accurately filled out and all activities required by the QC department are fulfilled. </span></li>\n\t<li><span style=\"font-family:Arial,Helvetica,sans-serif\">Other duties may be assigned.&nbsp; </span></li>\n</ul>\n",
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    "qualifications": "<p style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\"><strong><em>Limits of Authority:&nbsp; </em></strong>Interprets work situations and expectations, handles issues which conform to Company policy and past practice, and refers to extraordinary situations to the Quality Control Supervisor or Quality Control Manager for guidance when necessary.</span></p>\n\n<p style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\"><strong>Essential Skills and Qualifications:</strong></span></p>\n\n<ul>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">High School Diploma or equivalent required.</span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Associate&#39;s Degree in a relevant field (e.g., Quality Control, Science, Engineering) preferred.</span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">3-5 years of experience in a Quality Control role within a regulated environment (FDA, USDA).</span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Excellent verbal and written communication skills.</span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Ability to clearly and effectively communicate complex technical information.</span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Ability to effectively resolve interpersonal conflicts within the QC Inspector group.</span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Strong understanding of mathematical concepts, including fractions, percentages, ratios, and proportions.</span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Familiarity with rounding rules and significant figures.</span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Strong analytical and problem-solving skills.</span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Ability to interpret and apply SAP protocols to various production processes.</span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Ability to make sound decisions and take decisive action to ensure product quality and safety.</span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Ability to identify and resolve quality issues promptly and effectively.</span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Proficiency in Microsoft Office Suite (Word, Excel, Outlook).</span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Familiarity with relevant quality control software and databases.</span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Strong leadership and mentorship skills.</span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Excellent organizational and time management skills.</span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Ability to work independently and as part of a team.</span></li>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Strong attention to detail and accuracy.</span></li>\n</ul>\n\n<p style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\"><strong>Work Environment: </strong></span></p>\n\n<p style=\"margin-left:48px; text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.&nbsp;</span><span style=\"font-family:Arial,Helvetica,sans-serif\">The noise level in the work environment is usually moderate.</span></p>\n\n<p style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\"><strong>Physical Demands:</strong></span></p>\n\n<p style=\"margin-left:48px; text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.</span></p>\n\n<ul>\n\t<li style=\"text-align:justify\"><span style=\"font-family:Arial,Helvetica,sans-serif\">Must be able to lift up to 50lbs on a regular basis. </span></li>\n</ul>\n\n<p><span style=\"font-family:Arial,Helvetica,sans-serif\">The above job description is not intended to be an all-inclusive list of duties and standards of the position.&nbsp; Incumbents will follow any other instructions, and perform any other related duties, as assigned by their supervisor. Employees will be required to perform overtime (OT) duties as requested by their manager.</span></p>\n\n<p><u><strong>Candidates selected for employment will be required to complete a pre-employment screening, including a drug test, employment verification, and education verification.</strong></u></p>\n",
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