Job Description:
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.
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 biophar...