Business Analyst - GXP

Maverick Technology Partners; Waltham (MA); Hybrid; USD 90,000 - 130,000; Full time

Job summary

Maverick Technology Partners is seeking a seasoned hybrid IT/PM/BA professional to support GMP-regulated life sciences IT initiatives in the MetroWest Boston area. The role focuses on quality systems process improvement and regulatory systems migration, coordinating with external vendors and MSPs.

Ideal candidates bring 5-7+ years in regulated environments, direct GxP and Veeva experience, and the ability to switch between analyst and PM work while communicating clearly with technical and

Qualifications

• 5-7+ years in business analysis, PM, or hybrid IT in regulated environments.
• Direct experience with GxP and Veeva.
• Proven ability to lead process improvement and requirements documentation.
• Experience supporting manufacturing, quality, or regulatory operations.

Responsibilities

• Own end-to-end quality systems process improvement projects.
• Support regulatory systems migration and coordinate with vendors/partners.

Skills

Business analysis

Project management

GxP compliance

Veeva experience

Process mapping

Regulatory operations

Stakeholder communication

Job description

Hybrid in MetroWest Boston. Do Not Apply If Not Local

No C2C- Must be able to work without sponsorship

Project

You will support IT initiatives within a GMP/regulated life sciences environment.

• Quality Systems Process Improvement: Own enhancement project end-to-end, including current-state and future-state process mapping, requirements gathering, deliverables management, scope control, and risk mitigation.
• Regulatory Systems Migration: Support a regulatory information management system migration/reconfiguration effort, coordinating closely with external technology vendors and managed service partners.

Must Haves:

• 5-7+ years of experience in a business analyst, project manager, or hybrid IT role, ideally supporting regulated (GxP/GLP/GMP) business functions
• Direct experience within a GxP and Veeva experience
• Demonstrated ability to lead or co-lead process improvement initiatives, including current-state/future-state mapping, requirements documentation, and roadmap development
• Experience supporting manufacturing, quality, or regulatory operations functions (as opposed to clinical operations)
• Ability to manage multiple priorities and shift between analyst-style and PM-style work depending on project needs
• Strong written and verbal communication skills, with the ability to produce clear documentation for both technical and non-technical audiences