Associate Director, IS Quality & Compliance

revolutionmedicines; Redwood City (CA); On-site; USD 180,000 - 240,000; Full time

Job summary

Revolution Medicines seeks an experienced leader to direct IS Quality and Compliance with a focus on CSV/CSA across GxP computerized systems. You will partner with Quality and business stakeholders to maintain inspection readiness and regulatory compliance, while developing teams and external resources.

The role reports to the Senior Director, IS Quality, Risk & Compliance, and requires hands-on leadership in risk-based validation, data integrity, and lifecycle management across enterprise

Qualifications

• Experience leading CSV programs for GxP systems.
• Strong knowledge of ALCOA+ data integrity and electronic records.

Responsibilities

• Lead day‑to‑day CSV program for IS.
• Serve as technical lead for CSV/CSA and electronic records.
• Ensure validation activities meet regulatory requirements and policies.
• Provide guidance on GxP regulations and standards for computerized systems.
• Mentor teams and coordinate resources across projects.
• Oversee lifecycle deliverables, deviations, CAPAs and change controls.
• Support inspection readiness and audit responses under senior leadership.

Skills

CSV leadership

GxP compliance

Data integrity

Regulatory understanding

Education

Bachelor's degree

Job description

Revolution Medicines seeks an experienced leader to direct IS Quality and Compliance with a focus on CSV/CSA across GxP computerized systems. You will partner with Quality and business stakeholders to maintain inspection readiness and regulatory compliance, while developing teams and external resources.

The role reports to the Senior Director, IS Quality, Risk & Compliance, and requires hands-on leadership in risk-based validation, data integrity, and lifecycle management across enterprise