GMP Compliance Specialist ensuring products meet GMP compliance requirements in production. Involves batch record reviews, monitoring, and training in a pharmaceutical company.
GMP Compliance Specialist ensuring products meet GMP compliance requirements in production. Involves batch record reviews, monitoring, and training in a pharmaceutical company.
Compliance Administrator at Flagship Homes supporting compliance in housing by managing documentation and asset data. Aiming to ensure regulatory adherence in Fire Safety and other domains.
Regulatory expert leading global strategy and execution for digital medical devices at Novartis. Drive regulatory direction across development, registration, and post - approval ensuring compliance.
Global Regulatory Affairs Associate Director managing regulatory submissions and strategies in a global context. Ensuring compliance and operational efficiency throughout the regulatory process.
Global Regulatory Affairs Director at Novartis leading regulatory strategies for development and marketed products. Involves managing submissions and team leadership, ensuring regulatory compliance.
Associate Director providing strategic and operational regulatory direction for medical device projects. Collaborating with cross - functional teams for successful global submissions and regulatory compliance.

Senior Clinical Pharmacist in Medical Affairs developing clinical programs and regulatory strategies for CVS Health's diverse healthcare solutions. Ensuring compliance and driving performance through analytics and cross - functional collaboration.
Associate Director providing regulatory direction for medical device products at Novartis. Leading strategies, ensuring compliance, and communicating with Health Authorities globally.
Global Program Regulatory Director responsible for regulatory strategies at Novartis, integrating inputs from health authorities and stakeholders to meet commercial objectives.
Global Regulatory Affairs Associate Director managing regulatory strategies for cardio - metabolic products and leading cross - functional collaboration for agency interactions in the pharmaceutical industry.
Director of CMC Regulatory Affairs managing regulatory strategies and team for pharmaceutical/biotech company. Oversee global regulatory submissions and compliance activities with authorities and internal teams.
Regulatory Affairs Student supporting documentation compliance for labeling in healthcare projects. Engaging in regulatory tasks and enhancing personal skills in a hybrid work setup.