Duration: 12 Months with possibility of extension and conversion to full-time
Location: San Diego, CA
Hours: 8 AM to 5 PM with possible overtime
Only W2 candidates are eligible for this position. Third-party or C2C candidates will not be considered.
Where you come in:
You serve as the Staff Operational Compliance Specialist on key project teams, providing expertise in Quality Systems, Regulatory Compliance, and operational excellence.
You drive operational compliance initiatives, including system remediation, process improvement, quality system reviews, and audit readiness activities.
You proactively identify compliance and procedural gaps across programs or sites and lead corrective and preventive actions to drive sustainable improvement.
You provide expert-level guidance in strengthening and governing the Quality Management System, including CAPA strategy, nonconformance management, process controls, and continuous improvement initiatives.
You partner with cross-functional teams to ensure compliance with FDA 21 CFR 820, ISO 13485, and other applicable regulatory requirements.
You represent the organization during internal audits and external regulatory inspections, supporting inspection readiness and regulatory responses.
You ensure adherence to Quality Compliance and Regulatory Compliance requirements across products, processes, and systems.
You drive enhancements within Design Controls, Pilot Manufacturing, and Manufacturing environments to improve compliance, quality system effectiveness, and operational performance.
Preferred experience includes Quality Engineering, Design Controls, Manufacturing, and Validation activities.
Day-to-Day Responsibilities: Operational compliance including:
Work-related years of experience: 10+ Years Required Skills :(top 3 non-negotiables):
Preferred Skills (nice to have):
Education: Requires a Bachelors degree (B.S in Science of Engineering)
Software Skills Required:
Staff Operational Compliance Specialist • San Diego, CA, United States
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