About this role
<p><span style="font-family:verdana, geneva, sans-serif;font-size:14.0pt;color:black"><strong>Job Title: Associate Manager, Quality Engineer</strong></span><br><span style="font-family:verdana, geneva, sans-serif;font-size:14.0pt;color:black"><strong>Job Code: 38048</strong></span><br><span style="font-family:verdana, geneva, sans-serif;font-size:14.0pt;color:black"><strong>Job Location: Palm Bay, FL</strong></span><br><span style="font-family:verdana, geneva, sans-serif;font-size:14.0pt;color:black"><strong>Job Schedule: 9/80: Employees work 9 out of every 14 days – totaling 80 hours worked, and have every other Friday off</strong></span><br><br><br></p> <p><span style="font-family:verdana, geneva, sans-serif;font-size:14.0pt;color:black"><strong>Job Description:</strong></span><br><span style="font-family:verdana, geneva, sans-serif;font-size:14.0pt;color:black">We're seeking a Program Quality Engineer to lead our commitment to product excellence. You'll take ownership of designing, developing, and implementing quality standards and testing methodologies that safeguard product integrity and accuracy. As a leader, you'll guide and inspire a team of Quality Technicians, providing direction and oversight while ensuring all work meets rigorous contractual and regulatory requirements. This is your chance to make a meaningful impact on product quality while developing your leadership skills in a dynamic environment.</span><br><br><span style="font-family:verdana, geneva, sans-serif;font-size:14.0pt;color:black"><strong><br>Essential Functions:</strong></span><br><span style="font-family:verdana, geneva, sans-serif;font-size:14.0pt;color:black">• Plans and establishes goals, objectives, tasking, coaching, and support as needed for a team of Quality Technicians with direct impact on immediate and long-term operational results for the department.</span><br><span style="font-family:verdana, geneva, sans-serif;font-size:14.0pt;color:black">• Coordinates and leads the resolution of non-conformances, including MRB, root cause analysis, developing and implementing corrective actions and verifying effectiveness of corrective actions taken for assigned programs.</span><br><span style="font-family:verdana, geneva, sans-serif;font-size:14.0pt;color:black">• Reviews product drawings and documents for completeness, correctness, and compliance with L3Harris document standards.</span><br><span style="font-family:verdana, geneva, sans-serif;font-size:14.0pt;color:black">• Runs or supports investigations into the cause for discrepancies and nonconformities to develop disposition and recommend corrective action plans. Leads material review board and Process Failure Mode Effects Analysis (PFMEA) activities.</span><br><span style="font-family:verdana, geneva, sans-serif;font-size:14.0pt;color:black">• Continuously looks for opportunities to make moderate to substantial improvements in processes, systems, solutions, or products to enhance performance of job area.</span><br><span style="font-family:verdana, geneva, sans-serif;font-size:14.0pt;color:black">• Works with Supply Chain to set up material acquisition and manages supplier corrective actions.</span><br><span style="font-family:verdana, geneva, sans-serif;font-size:14.0pt;color:black">• Perform audits of quality control processes, identifying areas for improvement and making recommendations for corrective action.</span><br><span style="font-family:verdana, geneva, sans-serif;font-size:14.0pt;color:black">• Trains team members on quality control processes, procedures, and policies, ensuring that they have the knowledge and skills necessary to perform their jobs effectively.</span><br><span style="font-family:verdana, geneva, sans-serif;font-size:14.0pt;color:black">• Occasional domestic travel.</span><br><br><br><span style="font-family:verdana, geneva, sans-serif;font-size:14.0pt;color:black"><strong>Qualifications:</strong></span><br><span style="font-family:verdana, geneva, sans-serif;font-size:14.0pt;color:black">• Bachelor’s Degree with a minimum 6 years prior relevant experience. Graduate Degree with a minimum of 4 years of prior related experience. In lieu of a degree, minimum of 10 years of prior related experience.</span><br><span style="font-family:verdana, geneva, sans-serif;font-size:14.0pt;color:black">• Active Top-Secret / SCI with Polygraph security clearance.</span><br><br><span style="font-family:verdana, geneva, sans-serif;font-size:14.0pt;color:black"><strong><br>Preferred Additional Skills:</strong></span><br><span style="font-family:verdana, geneva, sans-serif;font-size:14.0pt;color:black">• Experience working programs requiring compliance to AS9100D, including the space addendum.</span><br><span style="font-family:verdana, geneva, sans-serif;font-size:14.0pt;color:black">• ASQ Certified Manager of Quality/Organizational Excellence (CMQ/OE) or Certified Quality Engineer (CQE).</span><br><span style="font-family:verdana, geneva, sans-serif;font-size:14.0pt;color:black">• Experience with Oracle Agile PLM, Windchill, Cincom, and DOORS software suites.</span><br><span style="font-family:verdana, geneva, sans-serif;font-size:14.0pt;color:black">• Supplier Quality / Supplier Development experience.</span><br><span style="font-family:verdana, geneva, sans-serif;font-size:14.0pt;color:black">• Skilled in the use of Microsoft Office Suite (Word, Excel, Power Point, etc.).</span><br><span style="font-family:verdana, geneva, sans-serif;font-size:14.0pt;color:black">• Practical knowledge in leading and managing projects, processes, and employees.</span><br><span style="font-family:verdana, geneva, sans-serif;font-size:14.0pt;color:black">• Strong knowledge and skills within the Quality profession.</span></p> <p> </p> <p><span style="font-family:verdana, geneva, sans-serif;font-size:14.0pt;color:white">#LI-FS1</span></p>