Veeva Configuration Analyst

We are seeking a highly motivated individual to participate in projects at life sciences companies, designing and deploying Quality systems. This role involves supporting Functional Analysts in workshops, leading customer discussions, and directly configuring and implementing Veeva Vault Quality Suite solutions.

What You'll Do:

• Participate in projects at life sciences companies

  designing and deploying Quality systems.

• Support Functional Analysts in workshops

  and be part of customer discussions of the Vault Quality suite (Vault QMS, Vault QualityDocs, Vault Training).
• Perform

  Quality/Content management solution design, prototyping, configuration, and documentation

  .

• Solution and configuration of Veeva Vault Quality Suite per customer requirements

  , including workflows, document types, security, fields, page layouts, reports, dashboards, formatted output reports, and notifications.
• Leverage enablement of

  out-of-the-box or best practices configuration approach

  to solution strategy.

• Assess the impact of change on the current configuration

  and work with key stakeholders to make informed decisions in a timely manner.

• Represent Professional Services across multiple engagements and workstreams

  (e.g., solution design and configuration, data migration, systems integration, etc.).

• Ensure customer success

  from the beginning to the end of the engagement lifecycle.

Requirements:

• 4+ years of experience implementing Document or Quality Management systems for life sciences

  as a consultant, business, or IT representative.

• Bachelor's Degree

  in Life Science, Computer Science, or a related field.

• Solid analytical and excellent interpersonal skills

  .

• Excellent communication skills

  (written and verbal).

• Strong attention to detail

  .

• Highly organized

  .
• Ability to act with speed to understand business requirements and willingness to

  roll up your sleeves to design and implement a solution

  .
• Exposure to

  life sciences compliance and computer systems validation requirements

  .

Nice to Have:

• Understanding of

  global quality requirements, compliance considerations, and processes

  for Quality process and content management, life sciences compliance, and/or computer systems validation.
• Proven track record

  leading high-impact global system implementation programs

  as a consultant, business, or IT lead, and/or business sponsor.
• Direct experience with systems, such as

  Veeva Vault, ETQ Reliance, Sparta TrackWise, OpenText, SharePoint, Documentum D2, FirstDoc, FirstPoint, NextDocs, UL ComplianceWire, and other quality information management or content management systems

  .

• SaaS/Cloud experience

  .
• Knowledge of

  Quality operations within the Life Sciences, Pharmaceutical, Biotech industry

  , and/or equivalent.