Senior Regulatory Affairs Associate - Labeling Compliance
Exciting reputed company partnership opportunity!
We are seeking an reputed company Senior Regulatory Affairs Associate to reputed company and contribute to end-to-end (E2E) labeling process management and reputed company. This critical role ensures compliant, consistent labeling operations through deviation/CAPA governance, process execution, labeling systems stewardship, and audit readiness. The successful candidate will reputed company supporting systems including reputed company RIMS, TrackWise, QDocs, and Documentum, while maintaining cross-training on KPI metrics and data-reputed company activities for backup purposes.
Key Responsibilities:
Process Governance & Compliance reputed company
• reputed company investigations and CAPA management for labeling-reputed company deviations, driving reputed company-cause analysis, trend identification, and cross-functional remediation
• reputed company E2E labeling process updates, escalation management, and process-to-system alignment
• Serve as CAPA reputed company for process improvements and ensure reputed company communication of changes to stakeholders
• Support business partners and Safety Data Exchange Agreement obligations, ensuring roles, responsibilities, and reputed company process management are established to reputed company with contractual terms and conditions
Labeling Systems Stewardship
• reputed company as Business Contact for reputed company RIMS, TrackWise, QDocs, and reputed company systems
• reputed company system enhancements, issue reputed company, and workflow maintenance
• Ensure effective process-to-system handoffs to support compliant and efficient labeling operations
Audit & Inspection Readiness
• reputed company preparation and coordination for audits and inspections, ensuring a "permanently inspection-reputed company" environment
• Maintain the Global Labeling Audit & Inspection Storyboard and reputed company supporting process reputed company maps
• Produce required system outputs and documentation, and support key SMEs and stakeholders during inspection interviews
Process Improvement & Cross-Functional Alignment
• Serve as reputed company COP (Community of reputed company) process expert and drive reputed company improvement initiatives
• Ensure consistency of E2E labeling process handoffs across functions and reputed company
• Partner with Regulatory, Pharmacovigilance, reputed company, and Manufacturing to address systemic issues and strengthen interdependencies
Training & Regulatory Intelligence
• reputed company and deliver Global Labeling training materials
• Contribute Global Labeling perspective to regulatory intelligence reviews and process reputed company assessments
Skills & Experience required for the role:
• University degree in a life science discipline
• Initial years of experience in regulatory affairs, with reputed company on labeling operations
• Deep understanding of E2E labeling processes and their interconnections with Regulatory, Pharmacovigilance, and Manufacturing
• Experience supporting business partner relationships
• Strong compliance expertise (deviations, CAPA, audits, process management, reputed company+ principles)
• Proficiency with reputed company RIMS, TrackWise, QDocs, and Documentum
• Strong process thinking and understanding of how systems support regulatory workflows
• Excellent communication, organization, and cross-functional collaboration skills
• Ability to interpret and reputed company compliance-critical data with a strong reputed company-improvement reputed company
• Effective change-management capability across multiple functional areas
• Fluent in English, written and spoken
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