GxP Document Control Lead — Veeva Expert

F. Hoffmann-La Roche AG; Holly Springs (MS); On-site; USD 78,000 - 144,000; Full time

Job summary

Genentech in Holly Springs is seeking a highly detail-oriented Document Control Specialist to ensure the integrity and compliance of quality and operational documents. You will manage document lifecycles, work with Engineering, MS&T, QC, and Quality Assurance, and embed best practices across the site.

You will lead Veeva Quality Documents workflows, configuration, and training, and own the site archival program, including retention scheduling and audits.

Qualifications

• Bachelor's degree in a scientific/technical field required.
• 5–8 years in a GxP environment with document control experience.
• 3+ years in document control, records management, or quality documentation at a manufacturing site.
• Experience with SOPs and regulatory documentation requirements.

Responsibilities

• Lead Veeva Quality Documents workflows, templates, and hierarchies.
• Collaborate with Engineering, MS&T, QC, and Operations to tailor workflows.
• Lead training on Veeva Quality Documents best practices.
• Ensure compliance with global GxP standards across documentation.

Skills

Veeva Quality Documents

Regulatory compliance

GxP experience

Documentation management

Cross-functional collaboration

Education

Bachelor's degree in a scientific/technical discipline

Tools

Veeva Quality Documents

Job description

Genentech in Holly Springs is seeking a highly detail-oriented Document Control Specialist to ensure the integrity and compliance of quality and operational documents. You will manage document lifecycles, work with Engineering, MS&T, QC, and Quality Assurance, and embed best practices across the site.

You will lead Veeva Quality Documents workflows, configuration, and training, and own the site archival program, including retention scheduling and audits.