Associate Director, Digital Quality Compliance

Scorpion Therapeutics; United States; Remote; USD 180,000 - 240,000; Full time

Job summary

Scorpion Therapeutics in the United States seeks an Associate Director for Quality Digital Capabilities to own and lead enterprise QA/QC digital systems, including SAP QM, Veeva Vault Quality, LIMS, and analytics dashboards.

You will shape digital roadmaps, ensure data integrity, drive validation strategies, manage changes, and align stakeholders across QA/QC functions in a fast-growing biotech environment.

Qualifications

• 8+ years in GxP Quality within biotech/pharma.
• Strong knowledge of Quality data domains (deviations, CAPA, change control).
• Expertise in GxP compliance, validation, and risk management.

Responsibilities

• Manage day-to-day administration, system validation, validation strategy, and continuous improvement of GxP-compliant digital systems supporting QA/QC functions; develop multi-year digital roadmaps; align stakeholders; evaluate new features; drive system integration, data integrity, and governance; oversee validation, change control, and documentation; facilitate governance forums.

Skills

GxP quality experience

Data governance

Cross-functional collaboration

Education

Bachelor's degree in Life Sciences, Engineering, or Computer Science

Tools

SAP QM

Veeva Vault Quality

Job description

Role

Associate Director for Quality Digital Capabilities, serving as business system owner and leader to shape, develop, and optimize enterprise Quality technologies like SAP, Veeva, LIMS, and analytics dashboards.

Responsibilities

• manage day-to-day administration, system validation, validation strategy, and continuous improvement of GxP-compliant digital systems supporting QA/QC functions; develop multi-year digital roadmaps; align stakeholders; evaluate new features; drive system integration, data integrity, and governance; oversee validation, change control, and documentation; and facilitate governance forums.

Requirements

• Bachelor's in Life Sciences, Engineering, or Computer Science; 8+ years in GxP Quality within biotech/pharma; extensive experience with SAP QM (5+ years), Veeva Vault Quality (7+ years), and related systems; strong knowledge of Quality data domains (deviations, CAPA, change control); expertise in GxP compliance, validation, and risk management.

Preferred

• experience translating complex data into insights for leadership, cross-functional collaboration skills.

High-Value

• focus on digital quality systems, GxP compliance, validation strategies, and enterprise-wide quality data management.

Work Setup

• Virtual; no travel specified.