Associate Specialist, Regulatory Affairs - Hybrid

Role: Support Global Regulatory Affairs within HRM Business Process Operations by managing system transition, process documentation, training, and compliance reporting for Veeva Registrations. Responsibilities: facilitate process updates, develop and support training materials, support change management and communication efforts, gather and document requirements, support change control processes, and maintain the HRM website for real-time user engagement. Requirements: BS/BA in Biology, Health Sciences, Information Systems, or related field; proficiency in MS Office, Veeva Vaults (particularly Veeva Registrations), website design; strong communication and collaboration skills; experience in documentation, regulatory processes, change management, and process implementation. Preferred: experience with regulatory applications, business systems, and results-oriented approach. HighValue: biopharma, regulatory affairs, Veeva platform, process documentation and training, cross-functional collaboration, 10% travel, hybrid work setup. Work setup: hybrid, US-based, with travel requirements.