A company is looking for a Lead Validation Specialist to oversee validation initiatives in compliance with regulatory standards.
Key Responsibilities
Lead and manage the validation team to ensure compliance with GxP and 21 CFR Part 11
Develop, execute, and maintain validation strategies and documentation for clinical systems
Collaborate cross-functionally with developers, QA, and SMEs to support validated environments
Required Qualifications
Bachelor's degree required
8+ years of professional experience in computer systems validation within life sciences or clinical research
5+ years leading a validation team or similar function
Proven expertise with GxP and 21 CFR Part 11 compliance
Strong technical foundation with relational databases (Oracle, MS SQL)
Validation Specialist • Saint Petersburg, Florida, United States