Quality Assurance Specialist
- Location
- North America/USA/Indiana/Princeton, IN
- Listed
- 2 days ago
About the role
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.
Job Summary
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.
Role Overview
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 entry-level 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.
Key Responsibilities
Independent Quality System Execution
- 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
Documentation Control & Records Management
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
Nonconformance & CAPA Coordination
- Independently document, track, and coordinate nonconformances and deviations
- Support root-cause analysis activities and CAPA development
- Track corrective and preventive actions to completion and perform effectiveness checks
Audit Support & Compliance Execution
Support internal, customer, and third-party audits with minimal supervision
Prepare audit evidence, participate in audits, and coordinate responses
- Track audit actions and ensure timely and effective closure
- Quality Data, Metrics & Reporting
- 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
- Cross-Functional Collaboration
Partner with Manufacturing, Operations, Engineering, Supply Chain, and Regulatory teams
Communicate quality requirements, findings, and expectations clearly
- Support implementation of corrective actions across functions
- Process Improvement & Standardization
- 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
Knowledge Sharing & Informal Mentorship
- 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
Education & Experience
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 follow-through
- Additional Job Details
- Professional - P2
- Organizational Impact
- Works to achieve operational, functional, and/or business targets within team with direct and indirect impact on departmental or job family results
- Intermediate-level professional; generally works independently under moderate supervision and may seek advice of more senior employees in the same area
- Works on smaller, less complex projects/assignments
Communication & Influence
- Communicates with employees typically within the department and/or job family, explaining and interpreting matters related to the department; may communicate with external clients or partners depending upon the job area
- May influence employees within own job area at an operational level
Innovation & Complexity
- Responsible for making minor improvements of processes, procedures, or systems to contribute to the performance of the team
- Problems faced may be difficult but are not complex and typically involve consideration of multiple issues and impact job family and/or multiple teams
Leadership & Talent Management
- May provide guidance, help with training and review work of entry-level employees
- May lead parts of less complex projects or processes
Knowledge & Experience
- Requires practical theoretical job knowledge and demonstrated competence within team typically obtained through advanced education and relevant experience
- Typically requires a bachelor's degree or equivalent experience and minimum 2 years of relevant experience
Equal opportunity and legal notices
Nidec is an Equal Employment Opportunity (EEO) and Affirmative 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.
- Work Shift Schedule
- First Shift (United States of America)
- No Soliciting
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.
From Nidec's careers page, first listed on Rolev.ai on November 8, 2026. Rolev.ai is not the employer.
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Common questions
Where is the Quality Assurance Specialist job at Nidec located?
This Quality Assurance Specialist position at Nidec is located in North America/USA/Indiana/Princeton, IN. Always check Nidec's application page for specific state eligibility or relocation policies.
How do I apply for the Quality Assurance Specialist position at Nidec?
This listing links directly to Nidec's Workday application page. You can apply directly on Nidec's site, or use Rolev.ai to check your resume fit, generate a zero-hallucination tailored resume and cover letter for this posting, and autofill the Workday application form in 1 click with the Rolev.ai Chrome extension. You always review the form and press Submit yourself.