Zealand Pharma Benefits Overview

Lead clinical trial inspection readiness and regulatory inspections; develop and maintain SOPs, records, and compliance documentation; provide GCP guidance; support CTIS and ClinicalTrials.gov submissions; collaborate cross-functionally to resolve compliance issues.

Lead and project-manage D365 F&O improvements for finance and supply chain, identify and implement AI use cases, translate business requirements into system solutions, manage vendors and stakeholders, drive process automation, change management, and user adoption.

Lead formulation development for monoclonal antibodies and antibody-drug conjugates from discovery through Phase 2. Design formulations, plan and execute lab-scale experiments and characterization, define manufacturing and scale-up strategies, manage tech transfer and CMO interactions, perform product/process risk assessments, and contribute to DS/DP specifications to ensure clinical supply readiness under GMP and CMC requirements.