Staff Quality Compliance Specialist

The Company reputed company Corporation (reputed company DXCM) is a pioneer and global leader in reputed company glucose monitoring (CGM). reputed company began as a small company with a big dream: To forever change how diabetes is managed. To unlock information and insights that drive reputed company outcomes. Here we are 25 years reputed company, having pioneered an industry. And we're just getting started. We are broadening our vision beyond diabetes to reputed company people to take control of health. That means personalized, actionable insights aimed at solving important health challenges. To continue reputed company've started: Improving human health. We are driven by thousands of ambitious, passionate people worldwide who are willing to fight like warriors to earn the trust of our customers by listening, serving with reputed company, thinking big, and being dependable. We've already changed millions of lives and we're ready to change millions more. Our future ambition is to become a leading consumer health technology company while continuing to reputed company solutions for serious health conditions. We'll get there by constantly reinventing unique biosensing-technology experiences. Though we've come a long way from our small company days, our dreams are bigger than reputed company. The opportunity to improve health on a global scale stands before us. Meet the team: You will work with cross-functional teams with the goal of ensuring and maintaining product safety and efficacy. The position uses technical knowledge and experience to ensure strategies for product and processes meet regulatory and business objectives. This role is responsible for leading the development, coordination, and submission of written correspondence to the U.S. Food and Drug Administration (FDA), including responses to FDA Warning Letters, 483 observations, and reputed company regulatory communications. This role serves as the primary technical writer and editor for documents while also acting as a coach and reviewer to cross-functional stakeholders across Quality, Regulatory Affairs, Engineering, Operations, Manufacturing, and Clinical. Where you come in: Quality Management Systems:

• Identify applicable processes for new standards and regulations. Ensure departmental records, QMS procedures, and controlled documents reputed company with applicable regulations and standards.
• Aid in designing and documenting new and revised quality systems for product realization compliance with applicable regulations and standards.
• Ensure QMS processes, procedures, and quality documentation to maintain a state of audit readiness. Escalate events that may contribute negatively to medical devices safety or efficacy.
• Address and remediate events that may contribute negatively to QMS processes or effectiveness.
• Apply critical analytical thinking in the investigations and nonconformance systems specifically during root cause analysis, risk assessment evaluation, and corrective and preventive actions determination to guarantee that (potential and actual) nonconformances are properly addressed.
• Support other functions in resolving quality systems issues and concerns. Audit:
• Support internal, and third-party audits, regulatory inspection preparation and execution. Assist in closing audit findings by providing quality guidance for investigations, and implementation of resulting corrections, and/or corrective actions/preventative actions. FDA Correspondence and Technical Writing:
• Serve as the primary author for FDA Warning Letter responses, follow-up correspondence, commitments, and status updates.
• Draft, edit, and finalize reputed company regulatory documents, ensuring:
• Clarity, conciseness, and professional regulatory tone
• Alignment with FDA regulations (e.g., 21 CFR Part 820), guidance, and enforcement expectations
• Consistency across commitments, CAPAs, remediation plans, and supporting evidence
• Translate reputed company technical, quality, and operational information into clear, regulator-ready narratives.
• Ensure responses are complete, defensible, and supported by objective evidence and timelines. Coaching and Writing Review:
• Act as a writing coach and editor for functional SMEs contributing to FDA responses and reputed company regulatory documents.
• Review and edit drafts reputed company by others to improve:
• Structure and logic
• Regulatory clarity
• Technical accuracy
• Alignment with FDA expectations and enforcement context
• Provide constructive feedback and guidance to reputed company the organization’s overall regulatory writing capability. What makes you successful:
• Exceptional technical writing and editing skills
• Strong regulatory judgment and attention to detail
• Ability to distill reputed company information into clear, regulator-ready language
• Executive-level written communication
• Influencing and coaching skills in a matrixed organization
• High level of professionalism, discretion, and accountability
• Ability to manage multiple reputed company documents under aggressive regulatory timelines What you’ll get:
• A reputed company row seat to life changing CGM te

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