Specialist, Lab Execution System, Tester

Drugdiscovery

Hyderabad, India
Hybrid
Gmp validation
Fda 21 cfr part 11
Regulated environment

Skills & Requirements

Must-have

  • GMP validation
  • FDA 21 CFR Part 11
  • regulated environment
  • test scripts
  • SDLC development

Nice-to-have

  • Agile methodologies
  • LIMS or LES experience
  • Biovia OneLab experience
  • Bachelor's degree

Key Requirements

  • 3-7 years in regulated GxP pharma lab environment
  • Understanding of regulatory requirements
  • Experience developing test scripts in a regulated environment

Work Rights

Not specified

Tailored Resume

Cover Letter