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Manage end-to-end artwork and labeling projects regionally, coordinating cross-functional teams and vendors to ensure compliant, on-time delivery. Oversee timelines, approvals, Veraciti/PLM issues, process improvements, RCA/CAPA, supervise Artwork Controllers, provide training, and support KPI reporting and cost/timeline tracking.

The Assistant - Operations will manage biometric systems, CCTV monitoring, vendor relations, finance coordination, and ensure operational efficiency within the office.

The Senior Statistical Programmer will program and validate datasets for clinical trials, oversee deliverables, manage projects, and ensure compliance with industry standards. Requires strong skills in SAS and R for statistical programming.

The Regulatory Affairs Specialist Consultant assists in regulatory documentation management, ensures compliance, performs completeness checks, and updates regulatory systems under supervision.

The Regulatory Affairs Analyst Consultant ensures timely submissions for market licenses, supports audits, and manages documentation while collaborating with stakeholders.

Lead analytical efforts in Real World Data research, develop specifications and methodologies, manage projects, and communicate findings to stakeholders.

The Regulatory Affairs Jr Analyst Consultant ensures regulatory data compliance, supports submission and approvals of market licenses, organizes tasks, and communicates with stakeholders.

Manage procurement for a pharmaceutical client: source and negotiate with suppliers across engineering, production, packaging, construction and capital services; process POs and invoices; perform bid analysis and reporting; implement category strategies with global team; drive cost savings, efficiency improvements, and strong supplier relationships while ensuring regulatory compliance.