Specialist, Qa Document Control

OXB

Durham, NC, US
On-site
Gmp document lifecycle management
Site documentation management system
Day-to-day document control activities
We’re on a mission to enable life-changing therapies to reach patients around the world—and we’re looking for passionate individuals who embody our core values every day: Responsible, Responsive, Resilient, and Respectful

Job Summary

  • We’re on a mission to enable life-changing therapies to reach patients around the world—and we’re looking for passionate individuals who embody our core values every day: Responsible, Responsive, Resilient, and Respectful.
  • Your responsibilities in this role would be: Ensures quality activities are carried out according to regulatory and quality requirements.
  • We offer competitive total reward packages, wellbeing programs, and career development opportunities to help you grow and thrive.

Matching Summary

We’re on a mission to enable life-changing therapies to reach patients around the world—and we’re looking for passionate individuals who embody our core values every day: Responsible, Responsive, Resilient, and Respectful.

Skills & Requirements

Must-have

  • GMP document lifecycle management
  • site documentation management system
  • day-to-day document control activities
  • eDMS and Veeva experience
  • Audit readiness support

Nice-to-have

  • passionate individuals
  • supportive, inclusive, and collaborative culture
  • future-focused and growing fast

Key Requirements

  • Bachelor’s degree or higher in Data/Information Management or related field
  • Minimum of 3 years GMP document control experience
  • Hands-on experience creation of GMP documents
  • Comprehensive knowledge of GMP regulations
  • Prior experience with electronic document management system (Veeva)

Work Rights

Not specified

Tailored Resume

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