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The Quality Assurance Specialist at Nidec Motor Corporation owns defined QMS processes, advancing from execution to independent ownership. You will drive document control, CAPA, audit support, and data integrity to ensure regulatory compliance.
Typically reporting to a Senior Quality Specialist or QA Manager, you will collaborate across Manufacturing, Operations, Engineering, and Regulatory teams to improve processes and ensure audit readiness and effective CAPA outcomes.
We begin with dreams. Dreams drive our motivation. Dreams are our future. The world's dreams, people's dreams, our dreams. Our passion creates ideas that make dreams come alive. Technology and products that were only dreams become reality.
All for dreams. Dreams challenge and the Nidec-Group will continue to meet the challenge. For the world's and people's tomorrows; the world's first, the world's best technologies and products; we will continue our part in creating a better society.
The Quality Assurance Specialist is an intermediate professional role responsible for independently executing and maintaining key Quality Management System (QMS) processes to ensure ongoing compliance with internal standards, customer requirements, and applicable regulations. This role applies strong procedural discipline, technical compliance knowledge, and professional judgment to support audit readiness, issue resolution, and continuous improvement.
The Quality Assurance Specialist owns one or more defined quality system processes or workstreams (e.g., document control, CAPA coordination, audit support, training compliance). The role moves beyond entrylevel execution into independent ownership, interpretation of requirements, and influence on compliance outcomes.
This position typically reports to a Senior Quality Specialist, Quality Systems Manager, Quality Manager, or Compliance Leader.
Independently execute assigned Quality Management System (QMS) processes.
Ensure quality activities are completed accurately, on time, and in compliance with procedures.
Serve as the point of accountability for defined quality system workstreams.
Manage the lifecycle of quality documents and records (creation, revision, approval, archiving).
Ensure documentation complies with internal policies and regulatory requirements.
Conduct periodic reviews to maintain document accuracy and relevance.
Independently document, track, and coordinate nonconformances and deviations.
Support rootcause analysis activities and CAPA development.
Track corrective and preventive actions to completion and perform effectiveness checks.
Support internal, customer, and thirdparty audits with minimal supervision.
Prepare audit evidence, participate in audits, and coordinate responses.
Track audit actions and ensure timely and effective closure.
Collect, verify, and maintain quality metrics and KPIs.
Ensure data accuracy and integrity across quality systems.
Support trend analysis and identification of recurring compliance issues.
Maintain training and qualification records for personnel.
Coordinate required training and monitor completion status.
Escalate training gaps or compliance risks as needed.
Partner with Manufacturing, Operations, Engineering, Supply Chain, and Regulatory teams.
Communicate quality requirements, findings, and expectations clearly.
Support implementation of corrective actions across functions.
Identify opportunities to improve quality system efficiency or clarity.
Support updates to quality procedures, templates, and workflows.
Apply lessons learned to strengthen compliance and execution discipline.
Provide informal guidance to Quality Assurance Specialist I roles.
Share best practices related to documentation, audits, and CAPA execution.
Support onboarding of new quality specialists as needed.
Bachelor's degree in Quality, Life Sciences, Engineering, Manufacturing, Business, or related field Preferred.
IPC -610 A Industry Printed Cricut board strongly recommended.
Typically, 2-4 years of experience in quality systems, compliance, audits, or regulated environments.
Working knowledge of Quality Management Systems and compliance requirements.
Ability to independently execute quality processes within defined scope.
Strong attention to detail and documentation discipline.
Ability to interpret and apply procedures, standards, and regulations.
Proficiency with document control systems and quality tracking tools.
Clear written and verbal communication skills.
Professional judgment, accountability, and strong followthrough.
Nidec is an Equal Employment Opportunity (EEO) and Affiantive Action Employer encouraging diversity in the workplace. All qualified applicants receive consideration for employment without regard to their age, gender, gender identity, sexual orientation, race, color, genetic information, religious creed, national origin, physical or mental disability, protected veteran status, or any other characteristic protected by law. For more information regarding your (EEO) rights as an applicant, please visit the following website: http://www1.eeoc.gov/employers/upload/eeoc_self_print_poster.pdf
First Shift (United States of America)
Nidec will not accept unsolicited resumes from individual recruiters or third party recruiting agencies in response to Nidec job postings. No fee will be paid to third parties who submit unsolicited candidates directly to our hiring managers. Pre-approval from the Nidec Talent Acquisition team is required before any external candidate can be submitted and such candidate must be submitted to the Nidec Talent Acquisition team.