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Veeva Vault Quality Jobs in Bothell, WA (NOW HIRING)

Veeva Vault Quality information

See Bothell, WA salary details

$11

$15

$19

How much do veeva vault quality jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for veeva vault quality in Bothell, WA is $15.61, according to ZipRecruiter salary data. Most workers in this role earn between $13.99 and $17.21 per hour, depending on experience, location, and employer.

What is Veeva Vault Quality?

Veeva Vault Quality is a cloud-based quality management system (QMS) designed specifically for the life sciences industry. It helps organizations manage quality processes such as document control, change control, training, and audits in a single platform. Veeva Vault Quality streamlines compliance, improves collaboration, and provides real-time visibility into quality data to ensure products meet regulatory standards.

What are some common challenges faced by professionals working with Veeva Vault Quality, and how can they be addressed?

Professionals working with Veeva Vault Quality often encounter challenges related to system configuration, change management, and ensuring regulatory compliance across global teams. It is common to face difficulties in standardizing processes and training end-users on new functionalities. These challenges can be addressed by fostering close collaboration with IT and quality assurance teams, participating in ongoing training, and leveraging Veeva's support resources to stay current with updates and best practices. Proactive communication and thorough documentation are also key to successful implementation and daily operation.

What are the key skills and qualifications needed to thrive as a Veeva Vault Quality specialist, and why are they important?

To thrive as a Veeva Vault Quality specialist, you need a solid background in quality management systems, life sciences regulations, and experience with document control processes, often supported by a relevant degree in life sciences or IT. Familiarity with Veeva Vault Quality Suite, GxP compliance, and data migration tools is typically required; certifications in Veeva Vault or similar platforms are highly valued. Strong analytical thinking, attention to detail, and effective communication skills help professionals excel in collaborating with cross-functional teams and managing complex quality processes. These competencies are crucial for ensuring regulatory compliance, process efficiency, and data integrity in highly regulated industries.

What is the difference between Veeva Vault Quality vs Veeva Vault Quality Associate?

AspectVeeva Vault QualityVeeva Vault Quality Associate
CertificationsGxP, Validation, ComplianceGxP, Validation, Compliance
Work EnvironmentRegulated industries, Quality departmentsRegulated industries, Quality teams
ResponsibilitiesSystem administration, validation, compliance oversightSupporting system users, data entry, basic validation tasks

Veeva Vault Quality professionals typically handle system validation, compliance, and administration within regulated industries, requiring specialized certifications. Veeva Vault Quality Associates support these systems through data management and user support, focusing on operational tasks. The roles differ mainly in responsibility level and scope, but both are essential in maintaining quality standards in life sciences companies.

What job categories do people searching Veeva Vault Quality jobs in Bothell, WA look for?

The top searched job categories for Veeva Vault Quality jobs in Bothell, WA are:

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Posted 3 days ago

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Job description

Job Description:
  • The CSV Engineer is responsible for ensuring that GxP computerized systems at the client site are validated in compliance with regulatory standards (21 CFR Part 11, EU Annex 11, GAMP 5).
  • This role directly supports gene therapy manufacturing operations by leading validation activities for key systems, including Veeva QMS, BMRAM, analytical lab instruments, and the Metasys Client.
  • By maintaining data integrity and system compliance, the CSV Engineer plays a critical part in ensuring product quality, patient safety, and regulatory inspection readiness.
Roles & Responsibilities:
  • uthor, review, and execute validation deliverables for GxP computerized systems, including Validation Plans, Requirements Specifications (URS/FS/DS), IQ/OQ/PQ protocols, Trace Matrices, and Validation Summary Reports.
  • Support computer system validation efforts for Veeva Vault QMS, BMRAM (laboratory information management), analytical lab instruments (e.g., HPLC, UHPLC, PCR instruments, plate readers etc.), ERP System (NetSuite).
  • Perform risk assessments to determine validation approach and ensure appropriate testing of system functionality, data integrity, and audit trail review.
  • Manage system change control, deviations, and CAPAs related to validated systems, ensuring compliance with Forge's quality system.
  • Collaborate with IT, QA, Lab Operations, and Facilities teams to support system upgrades, patches, and periodic reviews while maintaining a validated state.
Requirements:
  • Bachelor's degree in Computer Science, Engineering, Life Sciences, or related field (or equivalent experience).
  • 5-7+ years of experience in Computer System Validation (CSV) within a GxP regulated environment (pharmaceutical, biotech, or medical device).
  • Working knowledge of GAMP 5, 21 CFR Part 11, EU Annex 11, and data integrity principles (ALCOA+).
  • Experience validating at least one of the following: Veeva Vault QMS, BMRAM, laboratory instrumentation (e.g., Waters, Agilent, Chromeleon, Softmax or similar), or a building management system (Client) like Metasys.
  • Strong technical writing skills and ability to execute protocols with minimal supervision.
  • Nice to have: BMRAM and analytical lab instruments experience.