Senior eDiscovery Specialist — Forensics & Automation

Roche; Indianapolis (IN); On-site; USD 108,000 - 200,000; Full time

Job summary

Roche is seeking an experienced eDiscovery Specialist to join the Digital Technology group. You will bridge RDT with Legal, Compliance and Investigations, leading defensible collection and preservation of ESI across diverse systems.

You will apply Microsoft Purview, Relativity and Cellebrite to optimize processes, automate workflows, and support litigation, investigations and regulatory requests in a global pharma environment.

Qualifications

• Bachelor's degree in Information Technology, Computer Science, or related field.
• 5+ years of hands-on eDiscovery, digital forensics, or IT incident response experience.
• Experience with legal holds and defensible data collection practices.

Responsibilities

• Data Preservation and Collection across enterprise landscape with defensible methods.
• Data Processing and Review management using Relativity and Purview Premium.
• eDiscovery Operations: time-sensitive data requests, chain of custody, SOPs and audits.
• eDiscovery Platform & Tool Management: maintain Purview, Relativity, Cellebrite, and Druva.
• Process Improvement & Automation: optimize collection workflows for OS updates and security features.
• Stakeholder Trust & Communication: liaise with legal/compliance teams and business partners.

Skills

Communication skills

Project management

Problem-solving

Adaptability

Multitasking

Education

Bachelor's degree in Information Technology or Computer Science

Tools

Microsoft Purview

Relativity

Cellebrite

Druva

Google Workspace

Slack

Job description

Roche is seeking an experienced eDiscovery Specialist to join the Digital Technology group. You will bridge RDT with Legal, Compliance and Investigations, leading defensible collection and preservation of ESI across diverse systems.

You will apply Microsoft Purview, Relativity and Cellebrite to optimize processes, automate workflows, and support litigation, investigations and regulatory requests in a global pharma environment.