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Manager, Quality Computerized System Validation (CSV) at Nuvalent, Inc. - ApplyBlast

Manager, Quality Computerized System Validation (CSV)

Nuvalent, Inc.

5 months ago

Remote

Full Time

Manager

3 applicants

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About this role

The Manager, Quality Computerized System Validation is responsible for maintaining the validation lifecycle of GxP-regulated computerized systems across the organization in a remote pharmaceutical operating model.

Skills

Qualifications

Bachelor’s DegreeVeeva QualityDocs

About Nuvalent, Inc.

nuvalent.com

Headquarters

Cambridge, Massachusetts, United States

Company Size

11-50 employees

Founded

2017

View Profile

Nuvalent, now a part of GSK following an acquisition completed in July 2026, is an oncology company that creates precisely targeted small-molecule therapies using deep expertise in chemistry and structure-based drug discovery. Its pipeline focuses on selective kinase inhibitors for genetically defined cancers, including ALK, ROS1, and HER2-driven solid tumors, with the goal of overcoming resistance and improving patient outcomes. The company has an approved therapy for locally advanced ROS1-positive non-small cell lung cancer, with lead programs including NVL-520, NVL-655, and NVL-330.