Senior Manager, Safety, Medical & Regulatory Quality - Hybrid

Role: Senior Manager, Safety, Medical & Regulatory Quality, overseeing quality assurance for safety, regulatory affairs, and medical activities within AbbVie’s R&D and non-R&D portfolios. Responsibilities: ensure continuous compliance with global regulations and AbbVie policies, support regulatory inspections, manage GxP activities, and provide expert quality guidance to cross-functional partners. Facilitate risk assessments, support process development, and contribute to audit readiness and metrics reporting. Lead quality initiatives across safety, RA, and MA functions, fostering a culture of open communication and continuous improvement. Requirements: Bachelor's degree in Biology, Nursing, Pharmacy, or related science; 5+ years in pharmaceutical quality assurance, pharmacovigilance, or regulatory affairs; strong knowledge of industry standards, global regulations, and GxP compliance; project management, communication, and influencing skills. Preferred: experience supporting regulatory inspections and working in fast-paced environments. HighValue: expertise in safety, pharmacovigilance, regulatory compliance, and quality systems within a global biopharma setting. Work setup: not specified; based in US or Puerto Rico, with potential for remote work.