{"schemaVersion":"jobsearcher.job.v1","id":"71ca03b910f061d2fa7fe0ff","url":"https://jobsearcher.com/jobs/71ca03b910f061d2fa7fe0ff","canonicalUrl":"https://jobsearcher.com/jobs/71ca03b910f061d2fa7fe0ff","title":"Senior Quality Engineer","description":"BEPC is actively looking for Senior Quality Engineer, in Irving, TX area!\nW2 Contract – 6 months with possible extensions!\n\nBenefits include medical, dental, vision, and life insurance\n\nPay Rate: $39.00 - $42.00/hour - Determined based on experience (Paid Weekly)\n\nWork Model: Onsite role\n\nNote : This is a W2 only role — C2C, C2H will not be considered\n\nSummary of the Role\nBEPC is seeking a highly motivated Sr. Quality Engineer to join our client’s site in Irving, TX. This role will support quality operations by providing routine quality assurance support for manufacturing and operational areas. The position evaluates manufacturing quality performance, develops criteria to monitor and improve existing processes, identifies and eliminates compliance risks, and supports quality assurance systems and manufacturing processes. The role also leads nonconformance investigations, supports validation activities, and applies quality engineering principles to drive continuous improvement and regulatory compliance.\n\nSummary of Duties and Responsibilities\n\nProvide leadership within the Quality Operations department to ensure quality objectives and goals are achieved.\n\nHelp develop and drive the strategic direction of quality operations and compliance initiatives.\n\nConduct failure investigations and collaborate with business partners to implement robust corrective solutions that prevent recurring quality issues.\n\nReview pending investigation reports requiring Quality Assurance approval.\n\nCoach and train employees responsible for generating investigations.\n\nEscalate extraordinary investigation situations to Quality Assurance management for final approval.\n\nSupport the facility in identifying and eliminating compliance risks.\n\nEnsure appropriate specifications and procedures related to products are utilized.\n\nEnsure adherence to compliance requirements and policies related to:\n\nExternal manufacturers\n\nPackaging and labeling\n\nProduct testing\n\nReturned goods\n\nProduct complaints\n\nProduct recalls\n\nSupport, consult, train, and lead quality improvement projects focused on reducing defects, minimizing waste, and increasing reliability.\n\nUtilize Quality Engineering tools and techniques to:\n\nDevelop quality plans\n\nConduct and participate in FMEA activities\n\nSupport reliability engineering activities\n\nConduct process and system audits\n\nAnalyze routine and test data to identify improvement opportunities.\n\nProvide statistical support for:\n\nSampling plan analysis\n\nDesign of Experiments (DOE)\n\nPareto analysis\n\nANOVA\n\nStatistical Process Control (SPC)\n\nOther statistical applications as required\n\nServe as technical reviewer for validation protocols and reports.\n\nInvestigate nonconforming material and determine root cause, corrective actions, and disposition recommendations for the Material Review Board.\n\nApply research and benchmarking activities to develop innovative quality solutions and support implementation.\n\nDevelop and report progress on personal performance objectives aligned with facility quality goals.\n\nPrioritize work to meet established deadlines.\n\nServe as the Quality Operations subject matter expert for assigned responsibility areas.\n\nGuide and coach Quality Operations Technicians in managing nonconforming product through the nonconforming system.\n\nDemonstrate independent application of:\n\nData Integrity (DI)\n\nGood Manufacturing Practices (GMP)\n\nGood Documentation Practices (GDP)\n\nCommunicate business-related issues and opportunities to the next level of management.\n\nFollow all Health, Safety, and Environmental practices.\n\nEnsure compliance with all federal, state, local, and company regulations, policies, and procedures.\n\nPerform other assigned duties as needed.\n\nMain Qualifications\n\nEducation : Bachelor's degree required. Strong preference for Engineering or a related technical field.\n\nExperience : Minimum of 4 years of related quality and manufacturing experience. Experience in an FDA-regulated environment. Experience in the medical device, pharmaceutical, or other highly regulated industry.\n\nRequired Knowledge, Skills & Abilities\n\nKnowledge of ISO 13485 and/or cGMP regulations.\n\nDemonstrated project management and project leadership skills.\n\nTechnical training and experience with:\n\nStatistics\n\nLean Manufacturing\n\nSix Sigma methodologies\n\nMeasurement System Analysis (MSA)\n\nStatistical Process Control (SPC)\n\nDesign of Experiments (DOE)Reliability methods\n\nHands‑on troubleshooting and problem‑solving skills.\n\nStrong technical understanding of manufacturing equipment and processes.\n\nKnowledge of:\n\nQuality System Regulation (21 CFR Part 820)\n\nISO 13485 requirements\n\nMedical Device Directive (MDD)\n\nCanadian Regulations.\n\nPreferred qualifications\n\nASQ Certification such as:\n\nCertified Quality Engineer (CQE)\n\nCertified Quality Manager (CQM)\n\nCertified Reliability Engineer (CRE)\n\nCertified Quality Auditor (CQA)\n\nProcess Excellence certification.\n\n#J-18808-Ljbffr","company":"Bepc","rawCompany":"bepc","city":"Irving","state":"TX","isRemote":false,"isActive":false,"createdAt":"2026-07-17T03:13:44.815Z","occupations":[{"code":"11-3051.01","title":"Quality Control Systems Managers","slug":"quality-control-systems-managers"},{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"},{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"}],"industries":[{"code":"541330","title":"Engineering Services","slug":"engineering-services"},{"code":"541990","title":"All Other Professional, Scientific, and Technical Services","slug":"all-other-professional-scientific-and-technical-services"},{"code":"541380","title":"Testing Laboratories and Services","slug":"testing-laboratories-and-services"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Senior Quality Engineer","description":"BEPC is actively looking for Senior Quality Engineer, in Irving, TX area!\nW2 Contract – 6 months with possible extensions!\n\nBenefits include medical, dental, vision, and life insurance\n\nPay Rate: $39.00 - $42.00/hour - Determined based on experience (Paid Weekly)\n\nWork Model: Onsite role\n\nNote : This is a W2 only role — C2C, C2H will not be considered\n\nSummary of the Role\nBEPC is seeking a highly motivated Sr. Quality Engineer to join our client’s site in Irving, TX. This role will support quality operations by providing routine quality assurance support for manufacturing and operational areas. The position evaluates manufacturing quality performance, develops criteria to monitor and improve existing processes, identifies and eliminates compliance risks, and supports quality assurance systems and manufacturing processes. The role also leads nonconformance investigations, supports validation activities, and applies quality engineering principles to drive continuous improvement and regulatory compliance.\n\nSummary of Duties and Responsibilities\n\nProvide leadership within the Quality Operations department to ensure quality objectives and goals are achieved.\n\nHelp develop and drive the strategic direction of quality operations and compliance initiatives.\n\nConduct failure investigations and collaborate with business partners to implement robust corrective solutions that prevent recurring quality issues.\n\nReview pending investigation reports requiring Quality Assurance approval.\n\nCoach and train employees responsible for generating investigations.\n\nEscalate extraordinary investigation situations to Quality Assurance management for final approval.\n\nSupport the facility in identifying and eliminating compliance risks.\n\nEnsure appropriate specifications and procedures related to products are utilized.\n\nEnsure adherence to compliance requirements and policies related to:\n\nExternal manufacturers\n\nPackaging and labeling\n\nProduct testing\n\nReturned goods\n\nProduct complaints\n\nProduct recalls\n\nSupport, consult, train, and lead quality improvement projects focused on reducing defects, minimizing waste, and increasing reliability.\n\nUtilize Quality Engineering tools and techniques to:\n\nDevelop quality plans\n\nConduct and participate in FMEA activities\n\nSupport reliability engineering activities\n\nConduct process and system audits\n\nAnalyze routine and test data to identify improvement opportunities.\n\nProvide statistical support for:\n\nSampling plan analysis\n\nDesign of Experiments (DOE)\n\nPareto analysis\n\nANOVA\n\nStatistical Process Control (SPC)\n\nOther statistical applications as required\n\nServe as technical reviewer for validation protocols and reports.\n\nInvestigate nonconforming material and determine root cause, corrective actions, and disposition recommendations for the Material Review Board.\n\nApply research and benchmarking activities to develop innovative quality solutions and support implementation.\n\nDevelop and report progress on personal performance objectives aligned with facility quality goals.\n\nPrioritize work to meet established deadlines.\n\nServe as the Quality Operations subject matter expert for assigned responsibility areas.\n\nGuide and coach Quality Operations Technicians in managing nonconforming product through the nonconforming system.\n\nDemonstrate independent application of:\n\nData Integrity (DI)\n\nGood Manufacturing Practices (GMP)\n\nGood Documentation Practices (GDP)\n\nCommunicate business-related issues and opportunities to the next level of management.\n\nFollow all Health, Safety, and Environmental practices.\n\nEnsure compliance with all federal, state, local, and company regulations, policies, and procedures.\n\nPerform other assigned duties as needed.\n\nMain Qualifications\n\nEducation : Bachelor's degree required. Strong preference for Engineering or a related technical field.\n\nExperience : Minimum of 4 years of related quality and manufacturing experience. Experience in an FDA-regulated environment. Experience in the medical device, pharmaceutical, or other highly regulated industry.\n\nRequired Knowledge, Skills & Abilities\n\nKnowledge of ISO 13485 and/or cGMP regulations.\n\nDemonstrated project management and project leadership skills.\n\nTechnical training and experience with:\n\nStatistics\n\nLean Manufacturing\n\nSix Sigma methodologies\n\nMeasurement System Analysis (MSA)\n\nStatistical Process Control (SPC)\n\nDesign of Experiments (DOE)Reliability methods\n\nHands‑on troubleshooting and problem‑solving skills.\n\nStrong technical understanding of manufacturing equipment and processes.\n\nKnowledge of:\n\nQuality System Regulation (21 CFR Part 820)\n\nISO 13485 requirements\n\nMedical Device Directive (MDD)\n\nCanadian Regulations.\n\nPreferred qualifications\n\nASQ Certification such as:\n\nCertified Quality Engineer (CQE)\n\nCertified Quality Manager (CQM)\n\nCertified Reliability Engineer (CRE)\n\nCertified Quality Auditor (CQA)\n\nProcess Excellence certification.\n\n#J-18808-Ljbffr","datePosted":"2026-07-17T03:13:44.815Z","dateModified":"2026-07-17T03:13:44.815Z","hiringOrganization":{"@type":"Organization","name":"Bepc","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Irving","addressRegion":"TX","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"71ca03b910f061d2fa7fe0ff"},"url":"https://jobsearcher.com/jobs/71ca03b910f061d2fa7fe0ff"}}