Veeva Vault System Senior Specialist (Night Shift: 6 PM - 2 AM EST)

Kindeva; Woodbury (MN); On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

Medical

Dental

Vision

Health Savings Accounts

Flexible Spending Accounts

Disability Benefits

Life Insurance

Voluntary Benefits

Paid Absences

401k Benefits

Job summary

Kindeva Drug Delivery in Woodbury, MN, is seeking a Senior Veeva Vault System Specialist to administer and optimize the Global Veeva system for Documents, Training and Quality Management. The role emphasizes GMP compliance, data integrity, and continuous improvement, with a 6 PM–2 AM EST shift and collaboration across QA, Validation, IT, and business SMEs to drive system stability and user satisfaction.

Responsibilities include configuration, access management, change control support, and

Qualifications

• Bachelor’s or Master’s degree in Engineering, Life Sciences, Pharmacy, or related field.
• Minimum 2 years of experience in Quality Systems, Document Control, IT systems support or life sciences business systems.
• Must be able to work 6 PM – 2 AM EST.
• Certified system administrator with Veeva or equivalent.
• GxP, data integrity, document control, training, change control, or QMS knowledge preferred.

Responsibilities

• Support routine Veeva Vault administration activities including user maintenance and access requests.
• Assist with configuration updates for document types, metadata, workflows, lifecycle states, templates, and roles.
• Provide first-line user support and triage issues for Veeva Vault Quality applications.
• Support document lifecycle activities including routing, version control, and archival.
• Create or update work instructions, quick reference guides, training materials, job aids, and communications.
• Assist with reports, dashboards, metrics, and data extracts for monitoring and decision-making.
• Participate in change control activities by documenting requirements and coordinating approvals.
• Collaborate with Quality, IT, Validation, Training, Document Control, and SMEs to improve processes.

Skills

Veeva Vault administration

Quality systems

Regulatory compliance

Change control

Data integrity

Documentation management

Validation support

Cross-functional collaboration

Microsoft Office

Education

Bachelor’s or Master’s degree in Engineering, Life Sciences, Pharmacy

Tools

Veeva Vault

IT systems support

Validation tools

Job description

11200 Hudson Rd, Woodbury, MN 55129, USA

Job Description

Posted Friday, August 14, 2026 at 5:00 AM

Our Work Matters

At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.

The Impact You Will Make

The Veeva Vault System Senior Specialist is responsible for administering and driving the Global Veeva administration related to Documents, Training and Quality Management System modules. This role ensures the system operates efficiently, securely and in compliance with regulatory requirements and internal policies while fostering a culture of quality, risk management, and continuous improvement.

Schedule

6:00 PM – 2:00 AM EST

Responsibilities

System Administration & Configuration

• Support routine Veeva Vault administration activities, including user account maintenance, role assignments, group membership updates, and access request processing in accordance with approved procedures.
• Assist with configuration updates for document types, metadata, workflows, lifecycle states, templates, controlled vocabularies, user roles, and permissions under the direction of senior administrators or system owners.
• Provide first-line user support for Veeva Vault Quality applications by triaging issues, answering basic system questions, documenting incidents, and escalating complex items as appropriate.
• Support document lifecycle activities such as controlled document routing, workflow troubleshooting, version control, issuance support, archival assistance, and metadata/data quality checks.
• Create or update work instructions, quick reference guides, training materials, job aids, and support communications for end users.
• Assist with reports, dashboards, metrics, and data extracts to support business monitoring, compliance reviews, and operational decision-making.
• Participate in change control activities by documenting requirements, supporting testing, coordinating approvals and ensuring updates are implemented in a controlled manner.
• Collaborate with Quality, IT, Validation, Training, Document Control, and business SMEs to support continuous improvement of Veeva Vault processes and user experience

Business Process Support

• Collaborate with cross-functional teams to understand requirements and translate them into system solutions.
• Support quality processes such as Change Control, CAPA, Deviations, Complaints, and Document Management.
• Ensure alignment with GMP and other regulatory requirements.

Global Governance & Standards

• Establish and maintain global Templates for SOPs, Forms, Documentation Management, and all Quality System Modules.
• Lead or participate in cross-functional governance forums, quality councils, and harmonization initiatives.

System Maintenance & Upgrades

• Assist with Veeva Vault release management activities, including impact assessment support, test script preparation, regression testing, defect documentation, and deployment readiness tasks.
• Support validation and compliance deliverables, including drafting test cases, test execution, evidence capture, deviation/defect documentation, traceability support, and maintenance of system documentation.
• Maintain documentation for system configuration and validation activities.

Collaboration & Stakeholder Engagement

• Work closely with site QA, Validation, Engineering, Automation, and IT teams to ensure alignment and consistent execution of quality programs.
• Collaborate with Quality, HR, IT, and business stakeholders to support onboarding and ongoing training

Data & Security Management

• Ensure data integrity, backup, and disaster recovery protocols are in place.
• Monitor system logs and security alerts; implement corrective actions as needed.

Requirements

• Must be able to work 6 PM – 2 AM EST
• Bachelor’s or Master’s degree in Engineering, Life Sciences, Pharmacy, or related field preferred not required.
• Bachelors +5 years or Masters +3 years of experience in the pharmaceutical or biotechnology industry
• Minimum 2 years of experience in Quality Systems, Document Control, IT systems support, regulated operations, validation support, or life sciences business systems.
• Basic understanding of GxP, data integrity, document control, training, change control, or QMS processes preferred.
• Strong attention to detail and ability to follow controlled procedures in a regulated environment.
• Ability to document issues clearly, capture objective evidence, and communicate status to stakeholders.
• Proficiency with Microsoft Office applications, especially Excel, Word, PowerPoint, Teams, and Outlook
• Ability to work independently and in a global, cross-functional team environment.
• Certified system administrator with Veeva or equivalent

The expected compensation range for this position represents a good faith estimate. The specific compensation offered to a candidate may vary based on factors including, but not limited to, the candidate’s relevant knowledge, training, skills, work location, and/or experience.

Benefits

• Medical
• Dental
• Vision
• Health Savings Accounts
• Flexible Spending Accounts
• Disability Benefits
• Life Insurance
• Voluntary Benefits
• Paid Absences
• 401k Benefits

Equal Opportunity Employer

Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state or local law.