Validation Engineer

*Summary:* A great opportunity for a Validation Engineer II to support QC laboratory equipment qualification activities within a world-class biopharmaceutical environment. This role ensures full compliance with cGMP, corporate quality standards, and regulatory expectations, all while contributing directly to patient safety and operational excellence. *Key Responsibilities:* * Perform equipment qualification per EQ policies and procedures * Partner with QC lab staff to define qualification requirements * Author, review & execute qualification protocols * Coordinate with vendors and cross-functional support teams * Identify quality, compliance, and operational gaps * Review/sign-controlled documentation per Genentech guidelines * Support QC operations with additional assignments *Requirements:* * BS/BA in a relevant scientific discipline (preferred). * Pharma or biopharma experience required. * Knowledge of cGMP regulations. * 2+ years in validation or equipment qualification (preferred). * Ability to manage schedules, shifting priorities, and deadlines. *Skills:* * Strong verbal & written communication. * Ability to influence and build relationships. * Strategic and execution-focused mindset. * High accountability and ownership of deliverables. *Environment:* * Standard office/lab setting with required safety protocols. Job Type: Contract Pay: Up to $35.00 per hour Expected hours: 40 per week Work Location: In person