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Regulatory Affairs Consultant
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The Ranger Group
Santa Clara, CA (In Person)
Full-Time
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Job Description
Regulatory Affairs Consultant The Ranger Group - 4.0 Santa Clara, CA Job Details Full-time 14 hours ago Qualifications FDA submissions Document review Regulatory submission editing and review Biomedical regulatory compliance Quality systems Document change management Full Job Description Regulatory Affairs Consultant We are seeking an experienced Regulatory Affairs Consultant to support sustaining activities for Class III medical devices. This role will focus on assessing and managing regulatory impact of manufacturing and process changes to ensure continued compliance with global regulatory requirements. Key Responsibilities Review, assess, and document regulatory impact of manufacturing, process, and validation changes Support change control activities, including regulatory strategy, submission impact assessments, and regulatory documentation updates. Provide regulatory input on process validation, revalidation, and verification activities for Class III devices. Collaborate with Quality, Manufacturing, and Engineering teams to ensure compliant implementation of changes. Support IDE-related activities as needed, including amendments and regulatory correspondence. Required Qualifications Proven experience supporting Class III medical devices. Hands-on experience reviewing and assessing manufacturing and validation change orders Solid understanding of FDA regulations, Quality System Regulation (21 CFR 820), and change control processes. Experience supporting IDE submissions or amendments.