QA Document Control Specialist

📋 Description

• Manage document control in EDMS (Veeva Quality Vault) for GXP docs.
• Support Phase III and commercial readiness documentation.
• Ensure proper classification, indexing, versioning, and archiving.
• Conduct audits to identify discrepancies and ensure compliance.
• Provide Veeva guidance and training for document control.
• Collaborate with cross-functional teams for document accuracy.

🎯 Requirements

• Bachelor's degree or relevant comparable background.
• 3-5 years QA in biotech/pharma, with 1-2 years' Veeva experience.
• Working knowledge of electronic document management systems; Veeva Quality Vault required.
• Knowledge of GXP regulatory requirements (FDA, EMA, ICH).
• Proficiency in Word, Excel, SharePoint, Adobe Acrobat, Smartsheet.
• Excellent organizational, communication, and problem-solving skills.

🎁 Benefits

• Culture anchored in C.O.R.E. values: Caring, Original, Resilient, Egoless.
• Fast-paced, dynamic environment with growth opportunities.
• Competitive compensation: base, bonus, equity, health benefits.
• Paid time off: three weeks, shutdowns, sick leave.
• Resources for professional development and growth.
• Regular all-team in-person meetings for collaboration.