Associate, Quality Records

Role: Regulatory Affairs Associate supporting vaccine research and development, focusing on compliance and documentation within GxP environments. Responsibilities: manage electronic workflows and records governance in systems like GDMS, Veeva, and ValGenesis; administer and troubleshoot ELN systems; ensure adherence to GLP and GCLP standards; develop and deliver compliance training; identify opportunities for process automation and digital innovation; support audit readiness and data integrity initiatives. Requirements: Bachelor's degree in a scientific, technical, or related field; proficiency in Microsoft Office and digital tools; strong organizational, communication, and attention to detail skills; self-motivated with a collaborative mindset. Preferred: experience in regulated pharma or biotech, familiarity with document management systems and GxP compliance, and knowledge of AI-enabled digital solutions. High-Value: vaccine research, electronic record management, GxP, regulatory compliance, process automation, hybrid work model, no travel specified.