Quality Specialist - GxP Electronic Systems - REVOLUTION Medicines

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers.  The company’s R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS proteins, and RAS Companion Inhibitors for use in combination treatment strategies. As a new member of the Revolution Medicines team, you will join other outstanding Revolutionaries in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.

The Opportunity:

• Provide Veeva Quality Platform business administration support, including configuration support, access management, and user assistance within validated GxP systems.

• Provide administrative support for quality systems including ComplianceWire, Inspection Management Systems, and DocuSign by coordinating user provisioning, overseeing training records, generating reports, and maintaining system documentation.

• Deliver instructor-led classroom training sessions for end users on Quality Platforms functionality and system workflows.

• Develop and maintain system reports and interactive dashboards to track key performance indicators (KPIs) and operational metrics.

• Support GxP training compliance by ensuring completeness and accuracy of training files, including CVs and job descriptions for GxP personnel.

• Update and manage internal content on RevMed’s intranet site, contributing to clear and effective interdepartmental communications.

• Execute and document test scripts for configuration changes to validated electronic systems, ensuring compliance with quality and regulatory requirements.

• Support the development and distribution of information newsletters and communications related to Veeva system configuration updates.

• Contribute to internal audit & inspection readiness by gathering records, generating reports, and ensuring document traceability within the electronic QMS.

Required Skills, Experience and Education:

• Bachelor’s degree in Life Sciences or related field (advanced degree preferred)

• 1-2 years of experience in GxP Quality Assurance within the pharmaceutical, biotechnology, or related regulated industry.

• Demonstrate ability to manage multiple tasks, prioritize effectively, and meet deadlines.

• Excellent written and verbal communication skills.

• Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, and Outlook).

• Experience with electronic Quality Management Systems (eQMS) such as Veeva Quality Suite

• Ability to work independently and collaboratively across cross-functional teams in a dynamic environment

Preferred Skills:

• Familiarity with Document Control, Training Compliance, Audit Management, GxP systems validation within a pharmaceutical quality system.

• Experience supporting change management in GxP systems.

• A continuous improvement mindset and willingness to take initiative in solving problems. 

  #LI-Hybrid #LI-JC1