Quality Management Systems Specialist
Lear Corporation - Job Location (country) Spain
Posted Jun 12, 2026
Benefits
- Parental leave
- Not verified
- Non-birth-parent leave
- Not verified
- Family-building benefits
-
- Fertility benefits: Not verified
- Adoption assistance: Not verified
- Surrogacy assistance: Not verified
- Mental health support
- Not verified
- Relocation assistance
- Not verified
- Childcare support
- Not verified
- Learning budget
- Not verified
- Verification
- Not verified checked Jun 7, 2026
- Salary
- Not verified
- 401(k) match
- Reported from DOL Form 5500 industry filing (not employer-specific)
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Market context
- U.S. role benchmark (BLS OEWS)
- $106,409 U.S. median for this role
- Projected growth (BLS Employment Projections)
- +7.7% - Faster than average
Matched to SOC 13-2011 - Finance aggregate by role bucket.
Source: U.S. Bureau of Labor Statistics, OEWS, May 2024 and Employment Projections, 2024-2034.
Schedule
- Shift type
- Not verified
- Weekend work
- Not verified
Company
- Equity
- Offered Verified - SEC 10-K source
Application
- Cover letter
- Not verified
- Assessment
- Not verified
- Deadline
- Not stated
Where they hire
State eligibility is not yet verified.
About this role
Quality Management Systems Specialist Job Location (country) Spain Job Description LEAR Valls manuf. plant is looking for a high‑skilled Quality Management Systems Specialist eager to join a global leader in automotive technology. We are a large multinational company based at the Electronics Campus in Valls (Tarragona, Spain). We are seeking a professional with strong knowledge of Quality Systems and a proactive approach to continuous improvement. The ideal candidate will: •Maintain, develop, and improve the Quality Management Systems (QMS) according to corporate and industry standards (ISO/IATF). •Ensure that documentation, procedures, and internal processes remain aligned with customer and certification requirements. •Support internal and external audits, coordinating preparation, execution, and follow‑up activities. •Coordinate the management of non‑conformities, corrective actions, and preventive measures. •Train and support the organization in QMS requirements, methodologies, and quality tools. Key Outcome •Strong ownership of the QMS, ensuring a robust, updated, and compliant system aligned with corporate and customer expectations. •Effective coordination of internal audits and improvement actions to reinforce process conformity. •High-quality documentation management: procedures, instructions, standards, forms, and records. •Strong communication and interpersonal skills, enabling effective collaboration with all departments. •Contribution to a culture of quality, standardization, and operational excellence. Job Requirements •Universit
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