Associate Specialist, Scientific Compliance

Role: Scientific Compliance Associate supporting Development Sciences activities at AbbVie, ensuring GxP adherence across research and product development. Responsibilities: manage and support document management processes, collaborate with global teams on compliance with quality and regulatory standards, act as central contact for Quality Intelligence, and contribute to process improvements within a cross-functional, team-driven environment. Qualifications: associate's degree (scientific preferred), 0-3 years of industry-related GxP experience, familiarity with document management systems (e.g., Veeva Vault, SharePoint), and basic understanding of R&D drug development or medical device processes. Skills include strong communication, organization, attention to detail, and working in fast-paced, global teams. High-Value: supporting biopharma R&D compliance, cross-functional collaboration, and documentation in a GxP-regulated environment. Work setup: unspecified; likely hybrid or on-site based on standard industry practices.