Quality System Specialist
Johnson & Johnson · Milpitas, CA
QualityFull-time$75k–$121kCompany career page
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Role summary
Johnson & Johnson seeks a Quality System Specialist in Milpitas, California to administer and improve the Quality Management System, ensuring compliance with FDA regulations and ISO standards. The role involves supporting document control, change management, audits, and cross-functional quality initiatives.
What they're looking for
- Bachelor's degree in scientific, engineering, business, or related field
- 2-5 years quality assurance, regulatory compliance, or related experience in regulated industry
- Medical device industry experience preferred
- Knowledge of FDA 21 CFR Part 820/QMSR and ISO 13485 standards
- Experience with eQMS platforms, Agile PLM, SAP, ETQ, or ComplianceWire
- Proficiency in CAPA, Change Control, Document Control, and audit processes
- Strong project management, analytical, and interpersonal skills
What you'll be doing
- Prepare and maintain quality metrics, dashboards, trend analyses, and performance reports
- Coordinate Quality Management System Review activities and support nonconformance and CAPA processes
- Administer document control, records management, and lifecycle management in electronic systems
- Assist with internal, external, supplier audits and regulatory inspections including remediation
- Collaborate cross-functionally to implement and continuously improve QMS processes
Privacy & handoff
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