Murata
Overview
Murata is a global leader in the design, manufacture and supply of advanced electronic materials, leading edge electronic components, and multi-functional, high-density modules. Murata innovations can be found in a wide range of applications from mobile phones to home appliances, and automotive applications to energy management systems and healthcare devices. Why Consider This Job Opportunity The Quality Engineering Specialist ensures products meet specifications and quality standards through inspection, testing, and accurate recordkeeping. This position supports day-to-day Quality Management System (QMS) activities such as incoming, in process, final inspection, nonconforming material control, calibration, document control, and change implementation on the production floor. The Quality Engineering Specialist provides exposure to FDA, ISO, and other regulatory requirements while working closely with Quality Engineers and cross functional teams. What To Expect (Essential Job Responsibilities)
Support corrective and preventive actions (CAPA) by gathering data, performing verification checks, and documenting results. Assist with document control tasks, including routing, controlled copy distribution, and ensuring current versions are available at points of use. Assist complaint investigations by coordinating sample pulls, conducting basic tests, and documenting observations. Participate in internal audits as an auditor in training, collecting objective evidence and supporting audit follow‑up. Miscellaneous Job Responsibilities
Collaborate with Production, Engineering, Supply Chain, and Regulatory to resolve quality issues. Help prepare for external audits and inspections by organizing records and retrieval of QMS documentation. Support regulatory submission activities by locating and assembling required QMS records. Participate in quality improvement initiatives and cross functional projects as directed. What Is Required (Qualifications)
Bachelor’s degree in Engineering, Life Sciences, or a related technical discipline. Familiar with quality system concepts (e.g., audit, CAPA, nonconforming product, document control). Experience in ISO‑certified environments (ISO 9001 or ISO 13485) or equivalent. Strong attention to detail, organization, and communication skills with the ability to work independently and in a team environment. How To Stand Out (Preferred Qualifications)
Experience in a medical device or other regulated industry (ISO 13485 and/or FDA 21 CFR Part 820). Experience with electronic QMS platforms and/or ERP systems. ASQ certification (e.g., CQI, CQT) or Internal Auditor training. Perks
Comprehensive benefits package including medical, dental, and vision insurance. Generous Paid Time Off including paid holidays and floating holidays. 401(k) employer match on retirement planning. Hybrid working schedule for eligible positions. Tuition reimbursement on approved programs. Flexible and health spending accounts. Talent Development program. Other
Minimum Salary: $66,002 Maximum Salary: $88,359 We consider various factors in determining actual pay including your skills, qualifications, and experience. In addition to salary, this position is eligible for incentive awards based on individual and business performance as well as competitive benefits. Seniority level
Entry level Employment type
Full-time Job function
Manufacturing and Quality Assurance Industries
Motor Vehicle Manufacturing
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Murata is a global leader in the design, manufacture and supply of advanced electronic materials, leading edge electronic components, and multi-functional, high-density modules. Murata innovations can be found in a wide range of applications from mobile phones to home appliances, and automotive applications to energy management systems and healthcare devices. Why Consider This Job Opportunity The Quality Engineering Specialist ensures products meet specifications and quality standards through inspection, testing, and accurate recordkeeping. This position supports day-to-day Quality Management System (QMS) activities such as incoming, in process, final inspection, nonconforming material control, calibration, document control, and change implementation on the production floor. The Quality Engineering Specialist provides exposure to FDA, ISO, and other regulatory requirements while working closely with Quality Engineers and cross functional teams. What To Expect (Essential Job Responsibilities)
Support corrective and preventive actions (CAPA) by gathering data, performing verification checks, and documenting results. Assist with document control tasks, including routing, controlled copy distribution, and ensuring current versions are available at points of use. Assist complaint investigations by coordinating sample pulls, conducting basic tests, and documenting observations. Participate in internal audits as an auditor in training, collecting objective evidence and supporting audit follow‑up. Miscellaneous Job Responsibilities
Collaborate with Production, Engineering, Supply Chain, and Regulatory to resolve quality issues. Help prepare for external audits and inspections by organizing records and retrieval of QMS documentation. Support regulatory submission activities by locating and assembling required QMS records. Participate in quality improvement initiatives and cross functional projects as directed. What Is Required (Qualifications)
Bachelor’s degree in Engineering, Life Sciences, or a related technical discipline. Familiar with quality system concepts (e.g., audit, CAPA, nonconforming product, document control). Experience in ISO‑certified environments (ISO 9001 or ISO 13485) or equivalent. Strong attention to detail, organization, and communication skills with the ability to work independently and in a team environment. How To Stand Out (Preferred Qualifications)
Experience in a medical device or other regulated industry (ISO 13485 and/or FDA 21 CFR Part 820). Experience with electronic QMS platforms and/or ERP systems. ASQ certification (e.g., CQI, CQT) or Internal Auditor training. Perks
Comprehensive benefits package including medical, dental, and vision insurance. Generous Paid Time Off including paid holidays and floating holidays. 401(k) employer match on retirement planning. Hybrid working schedule for eligible positions. Tuition reimbursement on approved programs. Flexible and health spending accounts. Talent Development program. Other
Minimum Salary: $66,002 Maximum Salary: $88,359 We consider various factors in determining actual pay including your skills, qualifications, and experience. In addition to salary, this position is eligible for incentive awards based on individual and business performance as well as competitive benefits. Seniority level
Entry level Employment type
Full-time Job function
Manufacturing and Quality Assurance Industries
Motor Vehicle Manufacturing
#J-18808-Ljbffr