Veeva QA & Document Control Specialist

NCBioImpact; Holly Springs (NC); On-site; USD 78,000 - 144,000; Full time

Job summary

Genentech in Holly Springs, North Carolina seeks a meticulous Document Control Specialist to ensure the integrity, accessibility, and regulatory compliance of quality and operational documents.

As part of the Document Control team, you will manage document lifecycles, work with Engineering, MS&T, QC, QA, and Operations, and implement standardized procedures and archival excellence across the site.

Qualifications

• Bachelor's degree in a scientific/technical discipline.
• Minimum of 5–8 years in a GxP environment with document control experience.
• Experience with Veeva Quality Documents system administration and support.
• Experience managing archival rooms and records retention.

Responsibilities

• Veeva Quality Documents management across business units.
• Cross-functional document lifecycle management with Engineering, MS&T, QC, QA, and Operations.
• Own site archival room, records classification, and retention workflows.

Skills

Attention to detail

Cross-functional collaboration

Regulatory compliance

Document control

GxP knowledge

Veeva admin

Education

Bachelor's degree in a scientific/technical discipline

Tools

Veeva Systems

Job description

Genentech in Holly Springs, North Carolina seeks a meticulous Document Control Specialist to ensure the integrity, accessibility, and regulatory compliance of quality and operational documents.

As part of the Document Control team, you will manage document lifecycles, work with Engineering, MS&T, QC, QA, and Operations, and implement standardized procedures and archival excellence across the site.