Description

You will manage document control processes within a pharmaceutical quality assurance environment.

Responsibilities

• Maintain document management systems in compliance with GMP standards.
• Ensure all documentation meets strict regulatory requirements and FDA guidelines.
• Support readiness for regulatory examinations and audits.
• Execute quality assurance protocols related to document lifecycle management.

Required Skills

• 2+ years of experience in Quality Assurance or Document Control.
• Direct experience with GMP (Good Manufacturing Practice).
• Knowledge of FDA regulatory requirements.
• Proficiency in Document Management systems.
• Experience managing documentation for regulatory examinations.
• Bachelor's degree or equivalent graduate-level education.

Key Skills

Education

ANY GRADUATE